Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes

Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties. Strain-release driven reactions have emerged as an atom- and step-economic strategy for the organic synthesis. Using this strategy, a variety...

Full description

Saved in:
Bibliographic Details
Published inTetrahedron chem Vol. 9; p. 100070
Main Authors Hu, Qian-Qian, Chen, Jie, Yang, Yang, Yang, Hui, Zhou, Ling
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.03.2024
Elsevier
Subjects
[1.1.1]Propellanes
Bicyclo[1.1.0]butanes
Strain-release transformation
[1.1.1]Propellanes
Strain-release transformation
Bicyclo[1.1.0]butanes
Online AccessGet full text

Cover

Abstract Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties. Strain-release driven reactions have emerged as an atom- and step-economic strategy for the organic synthesis. Using this strategy, a variety of functional ring molecules have been efficiently synthesized, including various cyclobutane molecules, bicyclo[2.1.1]hexanes, bicyclo[1.1.1]pentanes, and others. More specifically, these strain release-driven reactions include aspects of nucleophilic addition, radical addition, electrophilic or transition metal catalysis. This review will discuss the recent developments in the strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes. [Display omitted]
AbstractList Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties. Strain-release driven reactions have emerged as an atom- and step-economic strategy for the organic synthesis. Using this strategy, a variety of functional ring molecules have been efficiently synthesized, including various cyclobutane molecules, bicyclo[2.1.1]hexanes, bicyclo[1.1.1]pentanes, and others. More specifically, these strain release-driven reactions include aspects of nucleophilic addition, radical addition, electrophilic or transition metal catalysis. This review will discuss the recent developments in the strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes.
Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties. Strain-release driven reactions have emerged as an atom- and step-economic strategy for the organic synthesis. Using this strategy, a variety of functional ring molecules have been efficiently synthesized, including various cyclobutane molecules, bicyclo[2.1.1]hexanes, bicyclo[1.1.1]pentanes, and others. More specifically, these strain release-driven reactions include aspects of nucleophilic addition, radical addition, electrophilic or transition metal catalysis. This review will discuss the recent developments in the strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes. [Display omitted]
ArticleNumber 100070
Author Zhou, Ling
Chen, Jie
Yang, Yang
Hu, Qian-Qian
Yang, Hui
Author_xml – sequence: 1
  givenname: Qian-Qian
  surname: Hu
  fullname: Hu, Qian-Qian
  organization: Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710127, China
– sequence: 2
  givenname: Jie
  surname: Chen
  fullname: Chen, Jie
  organization: Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710127, China
– sequence: 3
  givenname: Yang
  surname: Yang
  fullname: Yang, Yang
  organization: Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710127, China
– sequence: 4
  givenname: Hui
  surname: Yang
  fullname: Yang, Hui
  email: yanghui@xust.edu.cn
  organization: College of Chemistry and Chemical Engineering, Xi'an University of Science and Technology, Xi'an, 710054, China
– sequence: 5
  givenname: Ling
  orcidid: 0000-0002-6805-2961
  surname: Zhou
  fullname: Zhou, Ling
  email: zhoul@nwu.edu.cn
  organization: Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710127, China
BookMark eNp9kMtKxDAUhoMoOOo8gZu-QGtO0qaThQsZvAyILlQQREKSnmiGTjMkVZi3t51REBducvnJ95PzHZH9LnRIyCnQAiiIs2XR23dcFYyyckgorekemTAhRC4reN7_dT4k05SWwxM2A2BSTsjdQx-17_KILeqE2XDrkgtxpXsfupQFlxlvN7YNL1BAQV_NR687TJnummwbwes6hjW27RifkAOn24TT7_2YPF1dPs5v8tv768X84ja3nEmaaydLUxnbDIthsqxsNTOOlRIr7WojOEBjNBdQYePAUQm1gUoIOeN1KbDkx2Sx622CXqp19CsdNypor7ZBiG9Kx97bFhVvEBzwqrY1LalgEmTDrbS2llJIXg9dctdlY0gpolPW99vxRzWtAqpGz2qptp7V6FntPA8s_8P-_OV_6nxH4aDo02NUyXrsLDY-ou2HGfy__Be5sZh1
CitedBy_id crossref_primary_10_1002_ange_202420831
crossref_primary_10_1002_anie_202416741
crossref_primary_10_1021_acscatal_4c04837
crossref_primary_10_1002_ange_202418239
crossref_primary_10_1039_D5QO00020C
crossref_primary_10_1055_a_2456_9789
crossref_primary_10_1021_acs_orglett_4c04519
crossref_primary_10_1016_j_ccr_2024_216136
crossref_primary_10_1021_acs_orglett_5c00710
crossref_primary_10_1002_ange_202405781
crossref_primary_10_1055_a_2406_3243
crossref_primary_10_1021_jacsau_4c00839
crossref_primary_10_1039_D4SC06334A
crossref_primary_10_1002_ange_202416741
crossref_primary_10_1002_chem_202404099
crossref_primary_10_1039_D4GC03193H
crossref_primary_10_1002_anie_202418239
crossref_primary_10_1002_anie_202420831
crossref_primary_10_1002_anie_202405781
crossref_primary_10_1021_acs_joc_4c01920
crossref_primary_10_1021_acs_orglett_4c01219
crossref_primary_10_1021_acs_orglett_5c00705
crossref_primary_10_1039_D4SC03893B
crossref_primary_10_1021_acscatal_4c05622
crossref_primary_10_1039_D4QO02245A
crossref_primary_10_1039_D4SC07243J
crossref_primary_10_1021_acs_jpca_4c08396
crossref_primary_10_1055_a_2402_6920
Cites_doi 10.1039/D3SC04457B
10.1021/acs.orglett.1c04071
10.1002/anie.202305043
10.1021/jacs.3c09789
10.1038/s41557-018-0181-x
10.1038/s41467-023-44653-6
10.1021/jacs.3c13080
10.1002/anie.201909655
10.1039/D3CC01955A
10.1039/C9CC07610G
10.1002/anie.201905531
10.1002/chem.201804225
10.1039/D2QO00186A
10.1002/adsc.202200281
10.1039/C8OB02812E
10.1021/acs.orglett.5b01888
10.1038/s41557-022-00979-0
10.1021/acs.orglett.9b02426
10.1126/science.aad6252
10.1039/C9CS00311H
10.1002/anie.198603121
10.1021/jacs.3c02961
10.1002/anie.202011739
10.1038/s41557-023-01135-y
10.1002/anie.201603951
10.1021/acscatal.3c00305
10.1021/acs.joc.1c02267
10.1039/D2QO00167E
10.1002/anie.201600766
10.1002/anie.201908951
10.3762/bjoc.15.114
10.1021/jo00216a027
10.1021/jo00001a058
10.1039/D3SC01373A
10.1021/jacs.1c03492
10.1021/jacs.6b13229
10.1002/anie.202011738
10.1021/jo00333a039
10.1021/acscatal.3c03681
10.1002/anie.202217064
10.1021/cr60302a003
10.1039/D1SC02386A
10.1039/C8SC01355A
10.1021/jacs.0c07357
10.1002/cber.18850180296
10.1039/D3SC05700C
10.1021/jo00333a040
10.1021/cr990094z
10.1021/acs.orglett.2c01721
10.1039/D3QO01019H
10.1002/anie.202308606
10.1021/jacs.0c07490
10.1021/jacs.9b03653
10.1007/s11426-020-9733-y
10.1016/S0040-4039(00)80361-5
10.1021/jacs.1c11244
10.1002/ejoc.202000679
10.1002/anie.202213508
10.1002/anie.202016156
10.1039/D1CS00529D
10.1039/D3CC01262J
10.1055/s-0037-1610314
10.1021/jacs.2c13740
10.1016/S0040-4039(00)85802-5
10.1021/jo00146a031
10.1002/cmdc.201700082
10.1002/(SICI)1099-0690(199909)1999:9<2079::AID-EJOC2079>3.0.CO;2-D
10.1039/D2SC03948F
10.1021/jacs.8b08605
10.1002/anie.202004183
10.1021/acs.orglett.2c01707
10.1021/jacs.3c08512
10.1038/s41557-023-01222-0
10.1002/anie.201914875
10.1039/D0CC01771J
10.1080/00304949509458453
10.1002/anie.202214507
10.1021/acscatal.3c05003
10.1002/chem.201905539
10.1002/anie.200600723
10.1021/jacs.2c05304
10.1038/s41586-022-04636-x
10.1021/acsmedchemlett.6b00281
10.1021/acs.bioconjchem.7b00790
10.1021/jo00216a028
10.1039/D3OB01036H
10.1021/jacs.2c09248
10.1021/jacs.3c08206
10.1055/s-0039-1690197
10.1021/jacs.2c02976
10.1039/D1CS00510C
10.1021/jm300094u
10.1002/anie.201706799
10.1021/acs.orglett.9b03999
10.1002/anie.202304771
10.1016/S0040-4039(01)83253-6
10.1126/science.adh9737
10.1002/1099-0690(200004)2000:7<1137::AID-EJOC1137>3.0.CO;2-2
10.1021/acscatal.2c04511
10.1021/jacs.7b11865
10.1021/acs.orglett.6b02051
10.1021/acs.chemrev.6b00005
10.1021/jacs.3c06525
10.1021/jacs.2c11501
10.1021/jacs.2c09045
10.1021/acs.orglett.1c00889
10.1016/S0040-4020(01)96386-0
10.1021/ja00192a043
10.1002/ajoc.201900589
10.1007/BF00962498
10.1021/ja802906k
10.1039/D0QO00460J
10.1515/pac-2019-1007
10.1016/S0040-4020(01)80112-5
10.1039/D2SC05100A
10.1002/jcc.23165
10.1021/acs.orglett.3c02332
10.1016/j.tetlet.2008.07.179
10.1002/anie.202204719
10.1002/chem.201704105
10.1021/jacs.9b10689
10.1021/jo00288a002
10.1002/anie.201810061
10.1021/jacs.0c00245
10.1021/acs.orglett.2c02345
10.1002/anie.202106352
10.1002/anie.202000140
10.1002/anie.202000548
10.1002/anie.202302199
10.1039/C4GC00013G
10.1016/S0040-4020(01)98361-9
10.1002/anie.202211892
10.1021/acs.orglett.3c03222
10.1038/s41586-020-2060-z
10.1038/s42004-022-00811-3
10.1080/00304949609356550
10.1021/acs.orglett.3c01877
10.1039/D1CC03141D
10.1039/D1SC01349A
10.1016/j.chempr.2020.06.015
10.1016/0009-2614(94)01174-5
10.1002/anie.202310066
10.1016/S0040-4039(00)85801-3
10.1021/acs.orglett.1c01004
10.1016/j.tet.2004.06.100
10.1002/anie.202111291
10.1002/anie.202009340
10.1021/jacs.1c04180
10.1021/jacs.3c03248
10.1021/ar50039a001
10.1021/ja00162a022
10.1021/acscatal.9b03190
10.1021/acs.orglett.1c03346
10.1021/ar500437h
10.1021/jo00254a038
10.1021/acs.orglett.9b02026
10.1016/j.tet.2023.133296
10.1039/D3SC03258B
10.1002/anie.202205103
10.1021/jacs.3c12894
10.1021/ja403811t
10.1039/D1SC01836A
10.1002/jcc.20615
10.1021/ja00028a029
10.1021/jacs.2c13298
10.1021/acs.joc.9b01947
10.1021/acs.orglett.0c02115
ContentType Journal Article
Copyright 2024 The Authors
Copyright_xml – notice: 2024 The Authors
DBID 6I.
AAFTH
AAYXX
CITATION
DOA
DOI 10.1016/j.tchem.2024.100070
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
DatabaseTitleList

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
DeliveryMethod fulltext_linktorsrc
EISSN 2666-951X
ExternalDocumentID oai_doaj_org_article_3de1f1357c704062919d3c9cc7996937
10_1016_j_tchem_2024_100070
S2666951X24000093
GroupedDBID 6I.
AAFTH
AAFWJ
AAXUO
AFPKN
AKRWK
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
EBS
FDB
GROUPED_DOAJ
M41
M~E
OK1
ROL
0R~
AALRI
AAYWO
AAYXX
ACVFH
ADCNI
ADVLN
AEUPX
AFJKZ
AFPUW
AIGII
AITUG
AKBMS
AKYEP
APXCP
CITATION
ID FETCH-LOGICAL-c3290-af94b5bcdb5bb2945c58bf249e5af7b6311dba3615edf1f0917b1566983746e43
IEDL.DBID DOA
ISSN 2666-951X
IngestDate Wed Aug 27 01:19:47 EDT 2025
Thu Apr 24 23:03:49 EDT 2025
Tue Jul 01 04:18:58 EDT 2025
Sat Apr 06 16:23:41 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords [1.1.1]Propellanes
Strain-release transformation
Bicyclo[1.1.0]butanes
Language English
License This is an open access article under the CC BY license.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3290-af94b5bcdb5bb2945c58bf249e5af7b6311dba3615edf1f0917b1566983746e43
ORCID 0000-0002-6805-2961
OpenAccessLink https://doaj.org/article/3de1f1357c704062919d3c9cc7996937
ParticipantIDs doaj_primary_oai_doaj_org_article_3de1f1357c704062919d3c9cc7996937
crossref_citationtrail_10_1016_j_tchem_2024_100070
crossref_primary_10_1016_j_tchem_2024_100070
elsevier_sciencedirect_doi_10_1016_j_tchem_2024_100070
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate March 2024
2024-03-00
2024-03-01
PublicationDateYYYYMMDD 2024-03-01
PublicationDate_xml – month: 03
  year: 2024
  text: March 2024
PublicationDecade 2020
PublicationTitle Tetrahedron chem
PublicationYear 2024
Publisher Elsevier Ltd
Elsevier
Publisher_xml – name: Elsevier Ltd
– name: Elsevier
References Schwartz, Smyth, Nashar, Gardiner, Malins (bib81) 2022; 24
Ni, Hu, Tan, Yu, Li, Deng (bib73) 2023; 62
Ueda, Walczak, Wipf (bib97) 2008; 49
Wiberg, Waddell (bib157) 1990; 112
Chen, Li, Ou, Xue, Deng (bib48) 2023; 25
Xu, Wang, Sun, Ouyang, Ding, Yu, Xu, Li (bib69) 2022; 61
McNamee, Thompson, Anderson (bib60) 2021; 143
Swindell, Patel (bib119) 1990; 55
Wu, Ma, Feng, Zhu (bib95) 2021; 50
Panish, Chintala, Fox (bib40) 2016; 55
Locke, Bernhard, Senge (bib8) 2019; 25
Yu, Lübbesmeyer, Studer (bib46) 2021; 60
Ma, Nhat Pham (bib9) 2020; 9
Bychek, Hutskalova, Bas, Zaporozhets, Zozulya, Levterov, Mykhailiuk (bib58) 2019; 84
Jiang, Zheng, Gao, Lan, Xu, Zhang, Chen (bib160) 2022; 9
Zhang, Zhuang, Wang, Liu, Li, Su, Chen, Zhang (bib36) 2018; 29
Fawcett, Biberger, Aggarwal (bib101) 2019; 11
Guo, Noble, Aggarwal (bib104) 2021; 60
Rigotti, Bach (bib65) 2022; 24
Lin, Chen, Liu, Xiang, Tan (bib107) 2023; 145
Schwärzer, Zipse, Karaghiosoff, Knochel (bib171) 2020; 59
Nugent, Sterling, Frank, Mousseau, Anderson (bib128) 2021; 23
Yu, Jing, Noble, Aggarwal (bib166) 2020; 59
Gianatassio, Lopchuk, Wang, Pan, Malins, Prieto, Brandt, Collins, Gallego, Sach, Spangler, Zhu, Zhu, Baran (bib5) 2016; 351
Ma, Sloman, Han, Bennett (bib56) 2019; 21
Cheng, Feng, Zhang, You (bib77) 2022; 51
Fawcett (bib10) 2020; 92
Liu, Jiang, Zhang, Mei, Li, Pan (bib143) 2023; 10
Kelly, Milligan, Tilley, Sodano (bib12) 2022; 13
Kanazawa, Uchiyama (bib7) 2019; 30
Gaoni, Tomazic (bib29) 1985; 50
Jung, Muir, Lindsay (bib99) 2023; 134
Silvi, Aggarwal (bib102) 2019; 141
Dilmaç, Spuling, de Meijere, Bräse (bib6) 2017; 56
Lopchuk, Fjelbye, Kawamata, Malins, Pan, Gianatassio, Wang, Prieto, Bradow, Brandt, Collins, Elleraas, Ewanicki, Farrell, Fadeyi, Gallego, Mousseau, Oliver, Sach, Smith, Spangler, Zhu, Zhu, Baran (bib32) 2017; 139
Ma, Pinto, Pham, Sloman, Han (bib57) 2020; 2020
Ioffe, Svyatkin, Nefedov (bib17) 1988; 37
Gaoni (bib27) 1989; 45
Amey, Smart (bib82) 1981; 46
McNamee, Haugland, Nugent, Chan, Christensen, Anderson (bib59) 2021; 12
Bär, Kirschner, Nieger, Bräse (bib147) 2018; 24
Shin, Kim, Hong (bib162) 2023; 13
Chang, Dougherty (bib83) 1981; 46
Kerner, Wipf (bib98) 2021; 23
Kraemer, Ghiazza, Ragan, Ni, Lutz, Neumann, Fettinger, Nöthling, Goddard, Cornella, Pitts (bib129) 2022; 61
Gao, Guo, Shi, Zhu, Yang, Xia (bib47) 2022; 364
de Robichon, Kratz, Beyer, Zuber, Merten, Bach (bib108) 2023; 145
Kaszynski, Michl (bib118) 1988; 53
Ren, Ke, Zhou, Jiao, Li, Cao, Wang, Gao, Wang (bib130) 2023; 62
Tokunaga, Sato, Kuwata, Miura, Fuchida, Matsunaga, Koyanagi, Ohdo, Shindo, Ojida (bib34) 2020; 142
Takatsuki, Aoyama, Murai, Arisawa, Sako (bib41) 2023; 59
Agasti, Beltran, Pye, Kaltsoyannis, Crisenza, Procter (bib71) 2023; 15
Gaoni (bib31) 1995; 27
Messner, Kozhushkov, de Meijere (bib164) 2000; 2000
Radhoff, Daniliuc, Studer (bib87) 2023; 62
Du, Xu, Xu, Yu, Jiang (bib161) 2022; 24
Baeyer (bib1) 1885; 18
Zhang, Wang, Wu, Zhu (bib152) 2020; 40
Meiboom, Snyder (bib14) 1971; 4
Huang, Keess, Molander (bib138) 2022; 13
Lasányi, Máth, Tolnai (bib168) 2022; 87
Schwartz, Zhang, Attard, Gardiner, Malins (bib35) 2020; 26
Livingstone, Siebold, Meyer, Martín-Heras, Daniliuc, Gilmour (bib106) 2022; 12
Milligan, Busacca, Senanayake, Wipf (bib33) 2016; 18
Guo, Zhu, Wang, Li, Hu, Zhang, Xu, Li (bib144) 2024; 14
Daniel Rehm, Ziemer, Szeimies (bib163) 1999; 1999
Denisenko, Garbuz, Shishkina, Voloshchuk, Mykhailiuk (bib63) 2020; 59
Saya, Vos, Kleinnijenhuis, van Maarseveen, Ingemann, Hiemstra (bib64) 2015; 17
Bellotti, Glorius (bib124) 2023; 145
Wipf, Walczak (bib66) 2006; 45
Liang, Paulus, Daniliuc, Glorius (bib93) 2023; 62
Wu, Hao, Ye, Jiang, Pombar, Song, Lin (bib43) 2018; 140
Wang, Huang, Li, Lu (bib80) 2022; 9
Turkowska, Durka, Gryko (bib11) 2020; 56
Owen, de Gaetano, Gaffney, Godson, Guiry (bib149) 2022; 24
Nguyen, Bossonnet, Wodrich, Waser (bib85) 2023; 145
Kleinmans, Pinkert, Dutta, Paulisch, Keum, Daniliuc, Glorius (bib67) 2022; 605
Panish, Chintala, Boruta, Fang, Taylor, Fox (bib39) 2013; 135
Coppola, Pillitteri, Van der Eycken, You, Sharma (bib132) 2022; 51
Tang, Huang, Wu, Xiao, Zhou, Xu, Wu, Qu, Feng (bib38) 2023; 14
Shelp, Walsh (bib172) 2018; 57
Mandanaro, Dailey (bib24) 1998; 75
Measom, Down, Hirst, Jamieson, Manas, Patel, Somers (bib22) 2017; 8
Gaoni (bib26) 1982; 23
Pratt, Aycock, King, Jui (bib44) 2020; 31
Wölfl, Winter, Li, Noble, Aggarwal (bib100) 2023; 62
Cioc, Ruijter, Orru (bib131) 2014; 16
Caputo, Arroniz, Dürr, Mousseau, Stepan, Mansfield, Anderson (bib148) 2018; 9
Jackson, Mock, Tetef, Zheng, Jones (bib55) 1985; 41
Li, Li, Xu, Pan (bib155) 2022; 24
Livesley, Sterling, Robertson, Goundry, Morris, Duarte, Aïssa (bib176) 2022; 61
Auberson, Brocklehurst, Furegati, Fessard, Koch, Decker, La Vecchia, Briard (bib23) 2017; 12
Wang, Erchinger, Lenz, Dutta, Daniliuc, Glorius (bib49) 2023; 145
Stepan, Subramanyam, Efremov, Dutra, O'Sullivan, DiRico, McDonald, Won, Dorff, Nolan, Becker, Pustilnik, Riddell, Kauffman, Kormos, Zhang, Lu, Capetta, Green, Karki, Sibley, Atchison, Hallgren, Oborski, Robshaw, Sneed, O'Donnell (bib21) 2012; 55
Zheng, Huang, Dhungana, Granados, Keess, Makvandi, Molander (bib88) 2022; 144
Levterov, Panasyuk, Pivnytska, Mykhailiuk (bib90) 2020; 59
He, Xie, Yao, Wu (bib114) 2020; 31
Dong, Yen-Pon, Li, Bhattacharjee, Jolit, Molander (bib139) 2022; 14
Huang, Keess, Molander (bib141) 2023; 62
Remy, Bochet (bib75) 2016; 116
Zhang, Li, Wang, Zhang, Zhang, Tu (bib94) 2021; 12
Vyas, Clarkson, Wills (bib169) 2021; 23
Srinivasu, Das, Chandu, Ghosh, Sureshkumar (bib145) 2023; 25
Zhang, Gevorgyan (bib111) 2022; 144
Kim, Ruffoni, Al-Faiyz, Sheikh, Leonori (bib135) 2020; 59
Walczak, Krainz, Wipf (bib4) 2015; 48
Bennett, Fawcett, Denton, Biberger, Fasano, Winter, Aggarwal (bib103) 2020; 142
Galasso (bib18) 1994; 230
Mykhailiuk (bib62) 2019; 17
Guin, Bhattacharjee, Harariya, Biju (bib37) 2023; 14
Chen, Cui, Chen, Shang, Zhang (bib146) 2024; 15
Wu, Xu, Liu, Wu, Zhu (bib151) 2020; 63
Denisenko, Garbuz, Voloshchuk, Holota, Al-Maali, Borysko, Mykhailiuk (bib91) 2023; 15
Huang, Keess, Molander (bib137) 2022; 144
Hughes, Scarlata, Chen, Burch, Gleason (bib170) 2019; 21
Zhang, Su, Zheng, Li, Deng (bib89) 2024
Shin, Lee, Choi, Kim, Hong (bib127) 2021; 60
Rout, Marghem, Lan, Leyssens, Riant (bib150) 2019; 55
Andersen, Ferey, Daumas, Bernardelli, Guérinot, Cossy (bib167) 2020; 22
Liang, Kleinmans, Daniliuc, Glorius (bib92) 2022; 144
Das, Pedada, Singha, Hari (bib52) 2024
Kleinmans, Dutta, Ozols, Shao, Schäfer, Thielemann, Chan, Daniliuc, Houk, Glorius (bib78) 2023; 145
Kanazawa, Maeda, Uchiyama (bib133) 2017; 139
Wiberg, Lampman, Ciula, Connor, Schertler, Lavanish (bib2) 1965; 21
Kaszynski, McMurdie, Michl (bib117) 1991; 56
Khoury, Goddard, Tam (bib16) 2004; 60
Yu, Noble, Bedford, Aggarwal (bib159) 2019; 141
Applequist, Wheeler (bib53) 1977; 18
Makarov, Brocklehurst, Karaghiosoff, Koch, Knochel (bib165) 2017; 56
Pramanik, Qian, Xiao, Chen (bib123) 2020; 7
Levin, Kaszynski, Michl (bib121) 2000; 100
Pickford, Ripenko, McNamee, Holovchuk, Thompson, Smith, Mykhailiuk, Anderson (bib156) 2023; 62
Li, Lan, Zhou, Li, Zhu, Yu, Jiang (bib142) 2023; 59
Livesley, Trueman, Robertson, Goundry, Morris, Aïssa (bib175) 2022; 24
Shi, Xu, Ni, Li, Pan (bib136) 2022; 24
Shelp, Ciro, Pu, Merchant, Hughes, Walsh (bib174) 2021; 12
Gaoni (bib25) 1982; 23
Anderson, Measom, Murphy, Poole (bib115) 2021; 60
Yasukawa, Håheim, Cossy (bib113) 2023; 21
Huang, Zheng, Keess, Molander (bib140) 2023; 145
Dhake, Woelk, Becica, Un, Jenny, Leitch (bib86) 2022; 61
Wiberg (bib15) 1986; 25
Bychek, Mykhailiuk (bib61) 2022; 61
Zhang, Smith, Le, McCarver, Shireman, Carruthers, MacMillan (bib134) 2020; 580
Pinkert, Das, Schrader, Glorius (bib110) 2021; 143
Kaszynski, Friedli, Michl (bib120) 1992; 114
Applequist, Renken, Wheeler (bib54) 1982; 47
Tang, Xiao, Wu, Zhou, Xu, Feng (bib74) 2023; 62
Huck, Sarlah (bib76) 2020; 6
Liu, Lin, Li, Xue, Li, Wang (bib70) 2023; 13
Dai, Han, Wang, Tian (bib105) 2021; 57
Dasgupta, Bhattacharjee, Tong, Guin, McNamee, Christensen, Biju, Anderson (bib42) 2024; 146
Ociepa, Wierzba, Turkowska, Gryko (bib51) 2020; 142
Yan, Liu, Feng, Shi (bib72) 2023; 25
Trongsiriwat, Pu, Nieves-Quinones, Shelp, Kozlowski, Walsh (bib173) 2019; 58
Wang, Shao, Das, Dutta, Chan, Daniliuc, Houk, Glorius (bib112) 2023; 381
Kondo, Kanazawa, Ichikawa, Shimokawa, Nagashima, Miyamoto, Uchiyama (bib153) 2020; 59
Golfmann, Walker (bib13) 2023; 6
Bär, Heinrich, Nieger, Fuhr, Bräse (bib125) 2019; 15
Dutta, Lee, Ozols, Daniliuc, Shintani, Glorius (bib79) 2024
Gaoni (bib30) 1988; 29
Yu, Yang, Wang, Ding, Xu, Wen, Xu, Li (bib84) 2023; 145
Gaoni, Tomazic, Potgieter (bib28) 1985; 50
Bishop (bib3) 1976; 76
Lasányi, Tolnai (bib158) 2019; 21
Shen, Popescu, Wang, de Lescure, Noble, Paton, Aggarwal (bib109) 2023; 145
Ernouf, Chirkin, Rhyman, Ramasami, Cintrat (bib45) 2020; 59
Walczak, Wipf (bib96) 2008; 130
Nugent, Arroniz, Shire, Sterling, Pickford, Wong, Mansfield, Caputo, Owen, Mousseau, Duarte, Anderson (bib126) 2019; 9
Pickford, Nugent, Owen, Mousseau, Smith, Anderson (bib154) 2021; 143
Polo, Andres, Silvi (bib19) 2007; 28
Xiao, Xu, Zhou, Wu, Tang, Liu, Wu, Feng (bib50) 2023; 14
Guo, Chang, Herter, Salome, Braley, Fessard, Brown (bib68) 2022; 144
Smith, Hand, Love, Hill, Magers (bib20) 2013; 34
McGarry, Johnston, Scaiano (bib116) 1989; 111
Delia, Lochert (bib122) 1996; 28
Milligan (10.1016/j.tchem.2024.100070_bib33) 2016; 18
Ioffe (10.1016/j.tchem.2024.100070_bib17) 1988; 37
Coppola (10.1016/j.tchem.2024.100070_bib132) 2022; 51
Nugent (10.1016/j.tchem.2024.100070_bib126) 2019; 9
Smith (10.1016/j.tchem.2024.100070_bib20) 2013; 34
Pinkert (10.1016/j.tchem.2024.100070_bib110) 2021; 143
Meiboom (10.1016/j.tchem.2024.100070_bib14) 1971; 4
Shelp (10.1016/j.tchem.2024.100070_bib174) 2021; 12
Zheng (10.1016/j.tchem.2024.100070_bib88) 2022; 144
Shen (10.1016/j.tchem.2024.100070_bib109) 2023; 145
Yu (10.1016/j.tchem.2024.100070_bib159) 2019; 141
Yan (10.1016/j.tchem.2024.100070_bib72) 2023; 25
Baeyer (10.1016/j.tchem.2024.100070_bib1) 1885; 18
Hughes (10.1016/j.tchem.2024.100070_bib170) 2019; 21
Panish (10.1016/j.tchem.2024.100070_bib40) 2016; 55
Wu (10.1016/j.tchem.2024.100070_bib43) 2018; 140
Schwärzer (10.1016/j.tchem.2024.100070_bib171) 2020; 59
Wölfl (10.1016/j.tchem.2024.100070_bib100) 2023; 62
Dong (10.1016/j.tchem.2024.100070_bib139) 2022; 14
Shelp (10.1016/j.tchem.2024.100070_bib172) 2018; 57
Shin (10.1016/j.tchem.2024.100070_bib162) 2023; 13
Anderson (10.1016/j.tchem.2024.100070_bib115) 2021; 60
Dilmaç (10.1016/j.tchem.2024.100070_bib6) 2017; 56
Nugent (10.1016/j.tchem.2024.100070_bib128) 2021; 23
Bellotti (10.1016/j.tchem.2024.100070_bib124) 2023; 145
Li (10.1016/j.tchem.2024.100070_bib155) 2022; 24
He (10.1016/j.tchem.2024.100070_bib114) 2020; 31
Fawcett (10.1016/j.tchem.2024.100070_bib10) 2020; 92
Ma (10.1016/j.tchem.2024.100070_bib56) 2019; 21
Gaoni (10.1016/j.tchem.2024.100070_bib26) 1982; 23
Denisenko (10.1016/j.tchem.2024.100070_bib63) 2020; 59
Walczak (10.1016/j.tchem.2024.100070_bib4) 2015; 48
Livingstone (10.1016/j.tchem.2024.100070_bib106) 2022; 12
Huck (10.1016/j.tchem.2024.100070_bib76) 2020; 6
Guin (10.1016/j.tchem.2024.100070_bib37) 2023; 14
Lasányi (10.1016/j.tchem.2024.100070_bib168) 2022; 87
Huang (10.1016/j.tchem.2024.100070_bib138) 2022; 13
Du (10.1016/j.tchem.2024.100070_bib161) 2022; 24
Tang (10.1016/j.tchem.2024.100070_bib38) 2023; 14
Silvi (10.1016/j.tchem.2024.100070_bib102) 2019; 141
Caputo (10.1016/j.tchem.2024.100070_bib148) 2018; 9
Locke (10.1016/j.tchem.2024.100070_bib8) 2019; 25
Khoury (10.1016/j.tchem.2024.100070_bib16) 2004; 60
Owen (10.1016/j.tchem.2024.100070_bib149) 2022; 24
Measom (10.1016/j.tchem.2024.100070_bib22) 2017; 8
Das (10.1016/j.tchem.2024.100070_bib52) 2024
Jung (10.1016/j.tchem.2024.100070_bib99) 2023; 134
Denisenko (10.1016/j.tchem.2024.100070_bib91) 2023; 15
Wang (10.1016/j.tchem.2024.100070_bib80) 2022; 9
Kanazawa (10.1016/j.tchem.2024.100070_bib7) 2019; 30
Delia (10.1016/j.tchem.2024.100070_bib122) 1996; 28
Lin (10.1016/j.tchem.2024.100070_bib107) 2023; 145
Lasányi (10.1016/j.tchem.2024.100070_bib158) 2019; 21
Cioc (10.1016/j.tchem.2024.100070_bib131) 2014; 16
Yu (10.1016/j.tchem.2024.100070_bib166) 2020; 59
Applequist (10.1016/j.tchem.2024.100070_bib53) 1977; 18
Kaszynski (10.1016/j.tchem.2024.100070_bib117) 1991; 56
Ociepa (10.1016/j.tchem.2024.100070_bib51) 2020; 142
Kondo (10.1016/j.tchem.2024.100070_bib153) 2020; 59
Golfmann (10.1016/j.tchem.2024.100070_bib13) 2023; 6
Kerner (10.1016/j.tchem.2024.100070_bib98) 2021; 23
Yu (10.1016/j.tchem.2024.100070_bib46) 2021; 60
Kanazawa (10.1016/j.tchem.2024.100070_bib133) 2017; 139
Bishop (10.1016/j.tchem.2024.100070_bib3) 1976; 76
Shi (10.1016/j.tchem.2024.100070_bib136) 2022; 24
Livesley (10.1016/j.tchem.2024.100070_bib175) 2022; 24
Ren (10.1016/j.tchem.2024.100070_bib130) 2023; 62
Galasso (10.1016/j.tchem.2024.100070_bib18) 1994; 230
Yu (10.1016/j.tchem.2024.100070_bib84) 2023; 145
Takatsuki (10.1016/j.tchem.2024.100070_bib41) 2023; 59
Bär (10.1016/j.tchem.2024.100070_bib125) 2019; 15
Zhang (10.1016/j.tchem.2024.100070_bib152) 2020; 40
Saya (10.1016/j.tchem.2024.100070_bib64) 2015; 17
Guo (10.1016/j.tchem.2024.100070_bib144) 2024; 14
Trongsiriwat (10.1016/j.tchem.2024.100070_bib173) 2019; 58
Rout (10.1016/j.tchem.2024.100070_bib150) 2019; 55
Wiberg (10.1016/j.tchem.2024.100070_bib2) 1965; 21
Ma (10.1016/j.tchem.2024.100070_bib9) 2020; 9
McNamee (10.1016/j.tchem.2024.100070_bib59) 2021; 12
Chang (10.1016/j.tchem.2024.100070_bib83) 1981; 46
Swindell (10.1016/j.tchem.2024.100070_bib119) 1990; 55
Huang (10.1016/j.tchem.2024.100070_bib137) 2022; 144
Kaszynski (10.1016/j.tchem.2024.100070_bib120) 1992; 114
Huang (10.1016/j.tchem.2024.100070_bib141) 2023; 62
Liu (10.1016/j.tchem.2024.100070_bib143) 2023; 10
Pramanik (10.1016/j.tchem.2024.100070_bib123) 2020; 7
Rigotti (10.1016/j.tchem.2024.100070_bib65) 2022; 24
Shin (10.1016/j.tchem.2024.100070_bib127) 2021; 60
McGarry (10.1016/j.tchem.2024.100070_bib116) 1989; 111
Agasti (10.1016/j.tchem.2024.100070_bib71) 2023; 15
Vyas (10.1016/j.tchem.2024.100070_bib169) 2021; 23
Dai (10.1016/j.tchem.2024.100070_bib105) 2021; 57
Ernouf (10.1016/j.tchem.2024.100070_bib45) 2020; 59
Xu (10.1016/j.tchem.2024.100070_bib69) 2022; 61
Kaszynski (10.1016/j.tchem.2024.100070_bib118) 1988; 53
Livesley (10.1016/j.tchem.2024.100070_bib176) 2022; 61
Levterov (10.1016/j.tchem.2024.100070_bib90) 2020; 59
Fawcett (10.1016/j.tchem.2024.100070_bib101) 2019; 11
Gaoni (10.1016/j.tchem.2024.100070_bib25) 1982; 23
Schwartz (10.1016/j.tchem.2024.100070_bib81) 2022; 24
Lopchuk (10.1016/j.tchem.2024.100070_bib32) 2017; 139
Tang (10.1016/j.tchem.2024.100070_bib74) 2023; 62
Liu (10.1016/j.tchem.2024.100070_bib70) 2023; 13
Gaoni (10.1016/j.tchem.2024.100070_bib28) 1985; 50
Wiberg (10.1016/j.tchem.2024.100070_bib157) 1990; 112
Schwartz (10.1016/j.tchem.2024.100070_bib35) 2020; 26
Mykhailiuk (10.1016/j.tchem.2024.100070_bib62) 2019; 17
Andersen (10.1016/j.tchem.2024.100070_bib167) 2020; 22
Zhang (10.1016/j.tchem.2024.100070_bib134) 2020; 580
Wu (10.1016/j.tchem.2024.100070_bib95) 2021; 50
Walczak (10.1016/j.tchem.2024.100070_bib96) 2008; 130
Pickford (10.1016/j.tchem.2024.100070_bib154) 2021; 143
Kelly (10.1016/j.tchem.2024.100070_bib12) 2022; 13
Zhang (10.1016/j.tchem.2024.100070_bib36) 2018; 29
McNamee (10.1016/j.tchem.2024.100070_bib60) 2021; 143
Dutta (10.1016/j.tchem.2024.100070_bib79) 2024
Panish (10.1016/j.tchem.2024.100070_bib39) 2013; 135
Mandanaro (10.1016/j.tchem.2024.100070_bib24) 1998; 75
Bär (10.1016/j.tchem.2024.100070_bib147) 2018; 24
Dasgupta (10.1016/j.tchem.2024.100070_bib42) 2024; 146
Polo (10.1016/j.tchem.2024.100070_bib19) 2007; 28
Gaoni (10.1016/j.tchem.2024.100070_bib29) 1985; 50
Zhang (10.1016/j.tchem.2024.100070_bib94) 2021; 12
Bennett (10.1016/j.tchem.2024.100070_bib103) 2020; 142
Radhoff (10.1016/j.tchem.2024.100070_bib87) 2023; 62
Amey (10.1016/j.tchem.2024.100070_bib82) 1981; 46
Gaoni (10.1016/j.tchem.2024.100070_bib30) 1988; 29
Kim (10.1016/j.tchem.2024.100070_bib135) 2020; 59
Tokunaga (10.1016/j.tchem.2024.100070_bib34) 2020; 142
Gao (10.1016/j.tchem.2024.100070_bib47) 2022; 364
Zhang (10.1016/j.tchem.2024.100070_bib89) 2024
Wang (10.1016/j.tchem.2024.100070_bib112) 2023; 381
Daniel Rehm (10.1016/j.tchem.2024.100070_bib163) 1999; 1999
Huang (10.1016/j.tchem.2024.100070_bib140) 2023; 145
Li (10.1016/j.tchem.2024.100070_bib142) 2023; 59
Auberson (10.1016/j.tchem.2024.100070_bib23) 2017; 12
Jackson (10.1016/j.tchem.2024.100070_bib55) 1985; 41
Guo (10.1016/j.tchem.2024.100070_bib104) 2021; 60
Bychek (10.1016/j.tchem.2024.100070_bib58) 2019; 84
Cheng (10.1016/j.tchem.2024.100070_bib77) 2022; 51
Pratt (10.1016/j.tchem.2024.100070_bib44) 2020; 31
Yasukawa (10.1016/j.tchem.2024.100070_bib113) 2023; 21
Kraemer (10.1016/j.tchem.2024.100070_bib129) 2022; 61
Gaoni (10.1016/j.tchem.2024.100070_bib31) 1995; 27
Wu (10.1016/j.tchem.2024.100070_bib151) 2020; 63
Stepan (10.1016/j.tchem.2024.100070_bib21) 2012; 55
Bychek (10.1016/j.tchem.2024.100070_bib61) 2022; 61
Pickford (10.1016/j.tchem.2024.100070_bib156) 2023; 62
Wipf (10.1016/j.tchem.2024.100070_bib66) 2006; 45
Dhake (10.1016/j.tchem.2024.100070_bib86) 2022; 61
Xiao (10.1016/j.tchem.2024.100070_bib50) 2023; 14
Ma (10.1016/j.tchem.2024.100070_bib57) 2020; 2020
Ueda (10.1016/j.tchem.2024.100070_bib97) 2008; 49
Applequist (10.1016/j.tchem.2024.100070_bib54) 1982; 47
Wiberg (10.1016/j.tchem.2024.100070_bib15) 1986; 25
Kleinmans (10.1016/j.tchem.2024.100070_bib67) 2022; 605
Gianatassio (10.1016/j.tchem.2024.100070_bib5) 2016; 351
Ni (10.1016/j.tchem.2024.100070_bib73) 2023; 62
Guo (10.1016/j.tchem.2024.100070_bib68) 2022; 144
Levin (10.1016/j.tchem.2024.100070_bib121) 2000; 100
Makarov (10.1016/j.tchem.2024.100070_bib165) 2017; 56
Chen (10.1016/j.tchem.2024.100070_bib48) 2023; 25
Turkowska (10.1016/j.tchem.2024.100070_bib11) 2020; 56
Nguyen (10.1016/j.tchem.2024.100070_bib85) 2023; 145
Liang (10.1016/j.tchem.2024.100070_bib93) 2023; 62
Messner (10.1016/j.tchem.2024.100070_bib164) 2000; 2000
Wang (10.1016/j.tchem.2024.100070_bib49) 2023; 145
Remy (10.1016/j.tchem.2024.100070_bib75) 2016; 116
de Robichon (10.1016/j.tchem.2024.100070_bib108) 2023; 145
Chen (10.1016/j.tchem.2024.100070_bib146) 2024; 15
Srinivasu (10.1016/j.tchem.2024.100070_bib145) 2023; 25
Jiang (10.1016/j.tchem.2024.100070_bib160) 2022; 9
Gaoni (10.1016/j.tchem.2024.100070_bib27) 1989; 45
Liang (10.1016/j.tchem.2024.100070_bib92) 2022; 144
Zhang (10.1016/j.tchem.2024.100070_bib111) 2022; 144
Kleinmans (10.1016/j.tchem.2024.100070_bib78) 2023; 145
References_xml – volume: 25
  start-page: 4590
  year: 2019
  end-page: 4647
  ident: bib8
  article-title: Nonconjugated hydrocarbons as rigid-linear motifs: isosteres for material sciences and bioorganic and medicinal chemistry
  publication-title: Chem. Eur J.
– volume: 21
  start-page: 7666
  year: 2023
  end-page: 7680
  ident: bib113
  article-title: Synthesis of 1,3-disubstituted bicyclo[1.1.1]pentanes by cross-coupling induced by transition metals–formation of C–C bonds, Org
  publication-title: Biomol. Chem.
– volume: 30
  start-page: 1
  year: 2019
  end-page: 11
  ident: bib7
  article-title: Recent advances in the synthetic chemistry of bicyclo[1.1.1]pentane
  publication-title: Synlett
– volume: 145
  start-page: 4304
  year: 2023
  end-page: 4310
  ident: bib84
  article-title: Selective [2σ + 2σ] cycloaddition enabled by boronyl radical catalysis: synthesis of highly substituted bicyclo[3.1.1]heptanes
  publication-title: J. Am. Chem. Soc.
– volume: 14
  start-page: 9696
  year: 2023
  end-page: 9703
  ident: bib38
  article-title: C(sp
  publication-title: Chem. Sci.
– volume: 144
  start-page: 7988
  year: 2022
  end-page: 7994
  ident: bib68
  article-title: Strain-release [2π + 2σ] cycloadditions for the synthesis of bicyclo[2.1.1]hexanes initiated by energy transfer
  publication-title: J. Am. Chem. Soc.
– volume: 1999
  start-page: 2079
  year: 1999
  end-page: 2085
  ident: bib163
  article-title: A facile route to bridgehead disubstituted bicyclo[1.1.1]pentanes involving palladium-catalyzed cross-coupling reactions
  publication-title: Eur. J. Org. Chem.
– volume: 112
  start-page: 2194
  year: 1990
  end-page: 2216
  ident: bib157
  article-title: Reactions of [1.1.1]propellane
  publication-title: J. Am. Chem. Soc.
– volume: 2000
  start-page: 1137
  year: 2000
  end-page: 1155
  ident: bib164
  article-title: Nickel- and palladium-catalyzed cross-coupling reactions at the bridgehead of bicyclo[1.1.1]pentane derivatives - a convenient access to liquid crystalline compounds containing bicyclo[1.1.1]pentane moieties
  publication-title: Eur. J. Org. Chem.
– volume: 17
  start-page: 2839
  year: 2019
  end-page: 2849
  ident: bib62
  article-title: Saturated bioisosteres of benzene: where to go next?
  publication-title: Org. Biomol. Chem.
– volume: 130
  start-page: 6924
  year: 2008
  end-page: 6925
  ident: bib96
  article-title: Rhodium(I)-Catalyzed cycloisomerizations of bicyclobutanes
  publication-title: J. Am. Chem. Soc.
– volume: 11
  start-page: 117
  year: 2019
  end-page: 122
  ident: bib101
  article-title: Carbopalladation of C–C σ-bonds enabled by strained boronate complexes
  publication-title: Nat. Chem.
– volume: 13
  start-page: 13325
  year: 2023
  end-page: 13332
  ident: bib162
  article-title: Three-component cyclobutylation via silver(I)-Catalyzed carbene transfer reactions with [1.1.1]Propellane
  publication-title: ACS Catal.
– volume: 60
  start-page: 675
  year: 2021
  end-page: 679
  ident: bib46
  article-title: Oligosilanes as silyl radical precursors through oxidative Si−Si bond cleavage using redox catalysis
  publication-title: Angew. Chem. Int. Ed.
– volume: 62
  year: 2023
  ident: bib93
  article-title: Catalytic formal [2π+2σ] cycloaddition of aldehydes with bicyclobutanes: expedient access to polysubstituted 2-oxabicyclo[2.1.1]hexanes
  publication-title: Angew. Chem. Int. Ed.
– volume: 55
  start-page: 3
  year: 1990
  end-page: 5
  ident: bib119
  article-title: Stereoselective construction of the taxinine AB system through a novel tandem aldol-Payne rearrangement annulation
  publication-title: J. Org. Chem.
– volume: 25
  start-page: 5308
  year: 2023
  end-page: 5313
  ident: bib145
  article-title: Metal-free photoredox four-component strategy to 1,3-functionalized BCP derivatives
  publication-title: Org. Lett.
– volume: 21
  start-page: 10057
  year: 2019
  end-page: 10062
  ident: bib158
  article-title: Copper-catalyzed ring opening of [1.1.1]Propellane with alkynes: synthesis of exocyclic allenic cyclobutanes
  publication-title: Org. Lett.
– volume: 15
  start-page: 535
  year: 2023
  end-page: 541
  ident: bib71
  article-title: A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres
  publication-title: Nat. Chem.
– volume: 142
  start-page: 5355
  year: 2020
  end-page: 5361
  ident: bib51
  article-title: Polarity-reversal strategy for the functionalization of electrophilic strained molecules via light-driven cobalt catalysis
  publication-title: J. Am. Chem. Soc.
– volume: 142
  start-page: 16766
  year: 2020
  end-page: 16775
  ident: bib103
  article-title: Difunctionalization of C–C σ-bonds enabled by the reaction of bicyclo[1.1.0]butyl boronate complexes with electrophiles: reaction development, scope, and stereochemical origins
  publication-title: J. Am. Chem. Soc.
– volume: 24
  start-page: 7323
  year: 2022
  end-page: 7327
  ident: bib161
  article-title: Synthesis of imidized cyclobutene derivatives by strain release of [1.1.1]Propellane, org
  publication-title: Letture
– volume: 37
  start-page: 1827
  year: 1988
  end-page: 1836
  ident: bib17
  article-title: Molecular-mechanical analysis of the structure of strained organic molecules. 6. [m.n.k]-Propellanes
  publication-title: Bull. Acad. Sci. USSR, Div. Chem. Sci.
– volume: 145
  start-page: 20716
  year: 2023
  end-page: 20732
  ident: bib124
  article-title: Strain-release photocatalysis
  publication-title: J. Am. Chem. Soc.
– volume: 2020
  start-page: 4581
  year: 2020
  end-page: 4605
  ident: bib57
  article-title: Synthetic studies of 2,2-difluorobicyclo[1.1.1]pentanes (BCP-F
  publication-title: Eur. J. Org. Chem.
– volume: 9
  start-page: 2149
  year: 2022
  end-page: 2153
  ident: bib80
  article-title: Diastereoselective synthesis of 1,1,3,3-tetrasubstituted cyclobutanes enabled by cycloaddition of bicyclo[1.1.0]butanes
  publication-title: Org. Chem. Front.
– volume: 59
  start-page: 3917
  year: 2020
  end-page: 3921
  ident: bib166
  article-title: 1,3-Difunctionalizations of [1.1.1]Propellane via 1,2-metallate rearrangements of boronate complexes
  publication-title: Angew. Chem. Int. Ed.
– volume: 9
  start-page: 5295
  year: 2018
  end-page: 5300
  ident: bib148
  article-title: Synthesis and applications of highly functionalized 1-halo-3-substituted bicyclo[1.1.1]pentanes
  publication-title: Chem. Sci.
– volume: 144
  start-page: 23685
  year: 2022
  end-page: 23690
  ident: bib88
  article-title: Photochemical intermolecular [3σ + 2σ]-cycloaddition for the construction of aminobicyclo[3.1.1]heptanes
  publication-title: J. Am. Chem. Soc.
– volume: 56
  start-page: 307
  year: 1991
  end-page: 316
  ident: bib117
  article-title: Synthesis of doubly bridgehead substituted bicyclo[1.1.1]pentanes. Radical transformations of bridgehead halides and carboxylic acids
  publication-title: J. Org. Chem.
– volume: 31
  start-page: 51
  year: 2020
  end-page: 54
  ident: bib44
  article-title: Radical α-C–H cyclobutylation of aniline derivatives
  publication-title: Synlett
– volume: 141
  start-page: 9511
  year: 2019
  end-page: 9515
  ident: bib102
  article-title: Radical addition to strained σ-bonds enables the stereocontrolled synthesis of cyclobutyl boronic esters
  publication-title: J. Am. Chem. Soc.
– volume: 34
  start-page: 558
  year: 2013
  end-page: 565
  ident: bib20
  article-title: Conventional strain energies of azetidine and phosphetane: can density functional theory yield reliable results?
  publication-title: J. Comput. Chem.
– volume: 9
  start-page: 2234
  year: 2022
  end-page: 2239
  ident: bib160
  article-title: Synthesis of tetrasubstituted alkenyl nitriles via cyanocarbene addition of [1.1.1]propellane
  publication-title: Org. Chem. Front.
– volume: 9
  start-page: 9568
  year: 2019
  end-page: 9574
  ident: bib126
  article-title: A general route to bicyclo[1.1.1]pentanes through photoredox catalysis
  publication-title: ACS Catal.
– volume: 139
  start-page: 17791
  year: 2017
  end-page: 17794
  ident: bib133
  article-title: Radical multicomponent carboamination of [1.1.1]Propellane
  publication-title: J. Am. Chem. Soc.
– volume: 145
  start-page: 5363
  year: 2023
  end-page: 5369
  ident: bib140
  article-title: A general and modular approach to BCP alkylamines via multicomponent difunctionalization of [1.1.1]Propellane
  publication-title: J. Am. Chem. Soc.
– volume: 351
  start-page: 241
  year: 2016
  end-page: 246
  ident: bib5
  article-title: Strain-release amination
  publication-title: Science
– volume: 55
  start-page: 14976
  year: 2019
  end-page: 14979
  ident: bib150
  article-title: A radical exchange process: synthesis of bicyclo[1.1.1]pentane derivatives of xanthates
  publication-title: Chem. Commun.
– volume: 24
  start-page: 1268
  year: 2022
  end-page: 1273
  ident: bib81
  article-title: Investigating bicyclobutane–triazolinedione cycloadditions as a tool for peptide modification
  publication-title: Org. Lett.
– volume: 18
  start-page: 2269
  year: 1885
  end-page: 2281
  ident: bib1
  article-title: Ueber polyacetylenverbindungen
  publication-title: Ber. Dtsch. Chem. Ges.
– volume: 61
  year: 2022
  ident: bib176
  article-title: Electrophilic activation of [1.1.1]Propellane for the synthesis of nitrogen-substituted bicyclo[1.1.1]pentanes
  publication-title: Angew. Chem. Int. Ed.
– volume: 14
  start-page: 6585
  year: 2023
  end-page: 6591
  ident: bib37
  article-title: Lewis acid-catalyzed diastereoselective carbofunctionalization of bicyclobutanes employing naphthols
  publication-title: Chem. Sci.
– volume: 59
  start-page: 7161
  year: 2020
  end-page: 7167
  ident: bib90
  article-title: Water-soluble non-classical benzene mimetics
  publication-title: Angew. Chem. Int. Ed.
– volume: 12
  start-page: 9262
  year: 2021
  end-page: 9274
  ident: bib94
  article-title: Recent development and applications of semipinacol rearrangement reactions
  publication-title: Chem. Sci.
– volume: 24
  start-page: 1373
  year: 2018
  end-page: 1382
  ident: bib147
  article-title: Alkyl and aryl thiol addition to [1.1.1]Propellane: scope and limitations of a fast conjugation reaction
  publication-title: Chem. Eur J.
– volume: 12
  start-page: 14507
  year: 2022
  end-page: 14516
  ident: bib106
  article-title: Skeletal ring contractions via I(I)/I(III) catalysis: stereoselective synthesis of cis-α,α-Difluorocyclopropanes
  publication-title: ACS Catal.
– volume: 145
  start-page: 23771
  year: 2023
  end-page: 23780
  ident: bib49
  article-title: syn-Selective difunctionalization of bicyclobutanes enabled by photoredox-mediated C–S σ-bond scission
  publication-title: J. Am. Chem. Soc.
– volume: 24
  start-page: 4609
  year: 2022
  end-page: 4614
  ident: bib136
  article-title: Radical multicomponent alkyl alkynylation of propellane via synergistic photoredox and copper catalysis
  publication-title: Org. Lett.
– volume: 28
  start-page: 857
  year: 2007
  end-page: 864
  ident: bib19
  article-title: New insights on the bridge carbon–carbon bond in propellanes: a theoretical study based on the analysis of the electron localization function
  publication-title: J. Comput. Chem.
– volume: 48
  start-page: 1149
  year: 2015
  end-page: 1158
  ident: bib4
  article-title: Ring-strain-enabled reaction discovery: new heterocycles from bicyclo[1.1.0]butanes
  publication-title: Acc. Chem. Res.
– volume: 56
  start-page: 12774
  year: 2017
  end-page: 12777
  ident: bib165
  article-title: Synthesis of bicyclo[1.1.1]pentane bioisosteres of internal alkynes and para-disubstituted benzenes from [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
– volume: 21
  start-page: 2749
  year: 1965
  end-page: 2769
  ident: bib2
  article-title: Bicyclo[1.1.0]butane
  publication-title: Tetrahedron
– volume: 50
  start-page: 11577
  year: 2021
  end-page: 11613
  ident: bib95
  article-title: Radical-mediated rearrangements: past, present, and future
  publication-title: Chem. Soc. Rev.
– year: 2024
  ident: bib89
  article-title: Eu(OTf)
– volume: 62
  year: 2023
  ident: bib100
  article-title: Strain-release driven epoxidation and aziridination of bicyclo[1.1.0]butanes via palladium catalyzed σ-bond nucleopalladation
  publication-title: Angew. Chem. Int. Ed.
– volume: 7
  start-page: 2531
  year: 2020
  end-page: 2537
  ident: bib123
  article-title: Photoinduced strategies towards strained molecules
  publication-title: Org. Chem. Front.
– volume: 144
  start-page: 20207
  year: 2022
  end-page: 20213
  ident: bib92
  article-title: Synthesis of polysubstituted 2-oxabicyclo[2.1.1]hexanes via visible-light-induced energy transfer
  publication-title: J. Am. Chem. Soc.
– volume: 6
  start-page: 9
  year: 2023
  ident: bib13
  article-title: Bicyclobutanes as unusual building blocks for complexity generation in organic synthesis
  publication-title: Commun. Chem.
– volume: 63
  start-page: 1025
  year: 2020
  end-page: 1029
  ident: bib151
  article-title: A practical access to fluoroalkylthio(seleno)-functionalized bicyclo[1.1.1]pentanes
  publication-title: Sci. China Chem.
– volume: 25
  start-page: 6184
  year: 2023
  end-page: 6188
  ident: bib48
  article-title: 2-Isopropylthioxanthone-Catalyzed divergent functionalization of bicyclo[1.1.0]butanes under visible-light irradiation
  publication-title: Org. Lett.
– volume: 31
  start-page: 3065
  year: 2020
  end-page: 3072
  ident: bib114
  article-title: Recent advances in the applications of [1.1.1]propellane in organic synthesis, Chin
  publication-title: Chem. Lett.
– volume: 60
  start-page: 212
  year: 2021
  end-page: 216
  ident: bib104
  article-title: α-Selective ring-opening reactions of bicyclo[1.1.0]butyl boronic ester with nucleophiles
  publication-title: Angew. Chem. Int. Ed.
– volume: 230
  start-page: 387
  year: 1994
  end-page: 390
  ident: bib18
  article-title: Theoretical study of the
  publication-title: Chem. Phys. Lett.
– volume: 46
  start-page: 4092
  year: 1981
  end-page: 4093
  ident: bib83
  article-title: 2,3-Diazabicyclo[2.1.1]hex-2-ene. Synthesis and thermal decomposition
  publication-title: J. Org. Chem.
– volume: 23
  start-page: 5219
  year: 1982
  end-page: 5220
  ident: bib25
  article-title: Aryl cyclobutyl sulfones by reduction of 1-arylsulfonylbicyclobutanes with lithium aluminium hydride. synthesis of racemic junionone
  publication-title: Tetrahedron Lett.
– volume: 62
  year: 2023
  ident: bib74
  article-title: Silver-catalyzed dearomative [2π+2σ] cycloadditions of indoles with bicyclobutanes: access to indoline fused bicyclo[2.1.1]hexanes
  publication-title: Angew. Chem. Int. Ed.
– volume: 13
  start-page: 11936
  year: 2022
  end-page: 11942
  ident: bib138
  article-title: One step synthesis of unsymmetrical 1,3-disubstituted BCP ketones via nickel/photoredox-catalyzed [1.1.1]propellane multicomponent dicarbofunctionalization
  publication-title: Chem. Sci.
– volume: 15
  start-page: 1155
  year: 2023
  end-page: 1163
  ident: bib91
  article-title: 2-Oxabicyclo[2.1.1]hexanes as saturated bioisosteres of the ortho-substituted phenyl ring
  publication-title: Nat. Chem.
– volume: 50
  start-page: 2948
  year: 1985
  end-page: 2957
  ident: bib29
  article-title: Bridgehead reactivity, nucleophilic and radical additions, and lithium aluminum hydride reduction of 1-(arylsulfonyl)bicyclobutanes: general access to substituted, functionalized cyclobutanes. Syntheses of (.+-.)-citrilol acetate, (.+-.)-junionone, and the tricyclo[3.3.0.01,4]octane and tricyclo[4.3.0.01,7]nonane ring systems
  publication-title: J. Org. Chem.
– volume: 13
  start-page: 11721
  year: 2022
  end-page: 11737
  ident: bib12
  article-title: Bicyclobutanes: from curiosities to versatile reagents and covalent warheads
  publication-title: Chem. Sci.
– volume: 381
  start-page: 75
  year: 2023
  end-page: 81
  ident: bib112
  article-title: Dearomative ring expansion of thiophenes by bicyclobutane insertion
  publication-title: Science
– volume: 111
  start-page: 3750
  year: 1989
  end-page: 3751
  ident: bib116
  article-title: Kinetics and mechanism of the reaction of diphenylcarbene with [1.1.1]propellane
  publication-title: J. Am. Chem. Soc.
– volume: 146
  start-page: 1196
  year: 2024
  end-page: 1203
  ident: bib42
  article-title: Stereoselective alder-ene reactions of bicyclo[1.1.0]butanes: facile synthesis of cyclopropyl- and aryl-substituted cyclobutenes
  publication-title: J. Am. Chem. Soc.
– volume: 25
  start-page: 312
  year: 1986
  end-page: 322
  ident: bib15
  article-title: The concept of strain in organic chemistry
  publication-title: Angew. Chem. Int. Ed.
– volume: 45
  start-page: 2819
  year: 1989
  end-page: 2840
  ident: bib27
  article-title: New bridgehead-substituted 1-(arylsulfonyl)bicyclo[1.1.0]butanes and some novel addition reactions of the bicyclic system
  publication-title: Tetrahedron
– volume: 26
  start-page: 2808
  year: 2020
  end-page: 2812
  ident: bib35
  article-title: Structurally diverse acyl bicyclobutanes: valuable strained electrophiles
  publication-title: Chem. Eur J.
– volume: 15
  start-page: 419
  year: 2024
  ident: bib146
  article-title: C−F bond activation enables synthesis of aryl difluoromethyl bicyclopentanes as benzophenone-type bioisosteres
  publication-title: Nat. Commun.
– volume: 61
  year: 2022
  ident: bib61
  article-title: A practical and scalable approach to fluoro-substituted bicyclo[1.1.1]pentanes
  publication-title: Angew. Chem. Int. Ed.
– volume: 47
  start-page: 4985
  year: 1982
  end-page: 4995
  ident: bib54
  article-title: Polar substituent effects in 1,3-disubstituted bicyclo[1.1.1]pentanes
  publication-title: J. Org. Chem.
– volume: 55
  start-page: 3414
  year: 2012
  end-page: 3424
  ident: bib21
  article-title: Application of the bicyclo[1.1.1]pentane motif as a nonclassical phenyl ring bioisostere in the design of a potent and orally active γ-secretase inhibitor
  publication-title: J. Med. Chem.
– volume: 61
  year: 2022
  ident: bib86
  article-title: Beyond bioisosteres: divergent synthesis of azabicyclohexanes and cyclobutenyl amines from bicyclobutanes
  publication-title: Angew. Chem. Int. Ed.
– volume: 10
  start-page: 4616
  year: 2023
  end-page: 4622
  ident: bib143
  article-title: Photocatalyzed radical multicomponent alkylacylation of [1.1.1]propellane to synthesize 1,3-disubstituted BCP ketones
  publication-title: Org. Chem. Front.
– volume: 84
  start-page: 15106
  year: 2019
  end-page: 15117
  ident: bib58
  article-title: Difluoro-substituted bicyclo[1.1.1]pentanes for medicinal chemistry: design, synthesis, and characterization
  publication-title: J. Org. Chem.
– volume: 40
  start-page: 3431
  year: 2020
  end-page: 3438
  ident: bib152
  article-title: Radical-mediated bromoalkylation of [1.1.1]propellane: synthesis of bromo-substituted bicyclo[1.1.1]pentane derivatives, chin
  publication-title: J. Org. Chem.
– volume: 12
  start-page: 7066
  year: 2021
  end-page: 7072
  ident: bib174
  article-title: Strain-release 2-azaallyl anion addition/borylation of [1.1.1]propellane: synthesis and functionalization of benzylamine bicyclo[1.1.1]pentyl boronates
  publication-title: Chem. Sci.
– volume: 56
  start-page: 5718
  year: 2020
  end-page: 5734
  ident: bib11
  article-title: Strain release–an old tool for new transformations
  publication-title: Chem. Commun.
– volume: 145
  start-page: 24466
  year: 2023
  end-page: 24470
  ident: bib108
  article-title: Enantioselective, intermolecular [π2+σ2] photocycloaddition reactions of 2(1H)-Quinolones and bicyclo[1.1.0]butanes
  publication-title: J. Am. Chem. Soc.
– volume: 56
  start-page: 5684
  year: 2017
  end-page: 5718
  ident: bib6
  article-title: Propellanes—from a chemical curiosity to “explosive” materials and natural products
  publication-title: Angew. Chem. Int. Ed.
– volume: 14
  start-page: 619
  year: 2024
  end-page: 627
  ident: bib144
  article-title: General and modular route to (Halo)alkyl BCP-heteroaryls enabled by
  publication-title: ACS Catal.
– volume: 60
  start-page: 8103
  year: 2004
  end-page: 8112
  ident: bib16
  article-title: Ring strain energies: substituted rings, norbornanes, norbornenes and norbornadienes
  publication-title: Tetrahedron
– volume: 141
  start-page: 20325
  year: 2019
  end-page: 20334
  ident: bib159
  article-title: Methylenespiro[2.3]hexanes via nickel-catalyzed cyclopropanations with [1.1.1]Propellane
  publication-title: J. Am. Chem. Soc.
– volume: 28
  start-page: 411
  year: 1996
  end-page: 441
  ident: bib122
  article-title: Synthesis of biudgehead-substttuted bicyclo[1.1.1]pentanes
  publication-title: A Review, Org. Prep. Proced. Int.
– volume: 15
  start-page: 1172
  year: 2019
  end-page: 1180
  ident: bib125
  article-title: Insertion of [1.1.1]propellane into aromatic disulfides
  publication-title: Beilstein J. Org. Chem.
– volume: 57
  start-page: 15857
  year: 2018
  end-page: 15861
  ident: bib172
  article-title: Synthesis of BCP benzylamines from 2-azaallyl anions and [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
– volume: 18
  start-page: 4300
  year: 2016
  end-page: 4303
  ident: bib33
  article-title: Hydrophosphination of bicyclo[1.1.0]butane-1-carbonitriles
  publication-title: Org. Lett.
– year: 2024
  ident: bib79
  article-title: Photoredox-enabled dearomative [2π + 2σ] cycloaddition of phenols
  publication-title: J. Am. Chem. Soc.
– volume: 12
  start-page: 590
  year: 2017
  end-page: 598
  ident: bib23
  article-title: Improving nonspecific binding and solubility: bicycloalkyl groups and cubanes as para-phenyl bioisosteres
  publication-title: ChemMedChem
– volume: 59
  start-page: 20515
  year: 2020
  end-page: 20521
  ident: bib63
  article-title: Saturated bioisosteres of ortho-substituted benzenes
  publication-title: Angew. Chem. Int. Ed.
– volume: 21
  start-page: 6800
  year: 2019
  end-page: 6804
  ident: bib170
  article-title: Aminoalkylation of [1.1.1]Propellane enables direct access to high-value 3-Alkylbicyclo[1.1.1]pentan-1-amines
  publication-title: Org. Lett.
– volume: 364
  start-page: 2140
  year: 2022
  end-page: 2145
  ident: bib47
  article-title: Transition metal-free radical α-oxy C−H cyclobutylation via photoinduced hydrogen atom transfer
  publication-title: Adv. Synth. Catal.
– volume: 62
  year: 2023
  ident: bib130
  article-title: Access to polysulfides through photocatalyzed dithiosulfonylation
  publication-title: Angew. Chem. Int. Ed.
– volume: 24
  start-page: 8821
  year: 2022
  end-page: 8825
  ident: bib65
  article-title: Bicyclo[2.1.1]hexanes by visible light-driven intramolecular crossed [2 + 2] photocycloadditions, org
  publication-title: Letture
– volume: 4
  start-page: 81
  year: 1971
  end-page: 87
  ident: bib14
  article-title: Nuclear magnetic resonance spectra in liquid crystals and molecular structure
  publication-title: Acc. Chem. Res.
– volume: 61
  year: 2022
  ident: bib129
  article-title: Strain-release pentafluorosulfanylation and tetrafluoro(aryl)sulfanylation of [1.1.1]Propellane: reactivity and structural insight
  publication-title: Angew. Chem. Int. Ed.
– volume: 145
  start-page: 21152
  year: 2023
  end-page: 21158
  ident: bib107
  article-title: Enantioselective synthesis of chiral cyclobutenes enabled by brønsted acid-catalyzed isomerization of BCBs
  publication-title: J. Am. Chem. Soc.
– volume: 9
  start-page: 8
  year: 2020
  end-page: 22
  ident: bib9
  article-title: Selected topics in the syntheses of bicyclo[1.1.1]Pentane (BCP) analogues
  publication-title: Asian J. Org. Chem.
– volume: 27
  start-page: 185
  year: 1995
  end-page: 212
  ident: bib31
  article-title: Synthesis of AMINOCYCLOBUTANE mono- and dicarboxylic acids and derivatives thereof from (PHENYLSULFONYL)BICYCLOBUTANES
  publication-title: Org. Prep. Proced. Int.
– volume: 41
  start-page: 1453
  year: 1985
  end-page: 1464
  ident: bib55
  article-title: Reactions of carbenes with bicyclobutanes and quadricyclane: cycloadditions with two σ bonds
  publication-title: Tetrahedron
– volume: 605
  start-page: 477
  year: 2022
  end-page: 482
  ident: bib67
  article-title: Intermolecular [2π+2σ]-photocycloaddition enabled by triplet energy transfer
  publication-title: Nature
– volume: 75
  start-page: 98
  year: 1998
  ident: bib24
  article-title: [1.1.1]propellane, Org
  publication-title: Synth. Met.
– volume: 145
  start-page: 16508
  year: 2023
  end-page: 16516
  ident: bib109
  article-title: Iridium-catalyzed asymmetric difunctionalization of C–C σ-bonds enabled by ring-strained boronate complexes
  publication-title: J. Am. Chem. Soc.
– volume: 116
  start-page: 9816
  year: 2016
  end-page: 9849
  ident: bib75
  article-title: Arene–Alkene cycloaddition
  publication-title: Chem. Rev.
– volume: 14
  start-page: 1068
  year: 2022
  end-page: 1077
  ident: bib139
  article-title: Exploiting the sp
  publication-title: Nat. Chem.
– volume: 29
  start-page: 1591
  year: 1988
  end-page: 1594
  ident: bib30
  article-title: Regiospecific additions of hydrazoic acid and benzylamine to 1-(arylsulfonyl)bicyclo[1.1.0]Butanes. Application to the synthesis of cis and trans 2,7-methanoglutamic acids
  publication-title: Tetrahedron Lett.
– volume: 144
  start-page: 12961
  year: 2022
  end-page: 12969
  ident: bib137
  article-title: Dicarbofunctionalization of [1.1.1]Propellane enabled by nickel/photoredox dual catalysis: one-step multicomponent strategy for the synthesis of BCP-aryl derivatives
  publication-title: J. Am. Chem. Soc.
– volume: 76
  start-page: 461
  year: 1976
  end-page: 486
  ident: bib3
  article-title: Transition metal catalyzed rearrangements of small ring organic molecules
  publication-title: Chem. Rev.
– volume: 143
  start-page: 7648
  year: 2021
  end-page: 7654
  ident: bib110
  article-title: Use of strain-release for the diastereoselective construction of quaternary carbon centers
  publication-title: J. Am. Chem. Soc.
– volume: 25
  start-page: 8116
  year: 2023
  end-page: 8120
  ident: bib72
  article-title: Hantzsch esters enabled [2π+2σ] cycloadditions of bicyclo [1.1.0] butanes and alkenes under photo conditions
  publication-title: Org. Lett.
– volume: 45
  start-page: 4172
  year: 2006
  end-page: 4175
  ident: bib66
  article-title: Pericyclic cascade reactions of (Bicyclo[1.1.0]butylmethyl)amines
  publication-title: Angew. Chem. Int. Ed.
– volume: 51
  start-page: 2145
  year: 2022
  end-page: 2170
  ident: bib77
  article-title: Visible-light induced dearomatization reactions
  publication-title: Chem. Soc. Rev.
– volume: 59
  start-page: 8225
  year: 2020
  end-page: 8231
  ident: bib135
  article-title: Divergent strain-release amino-functionalization of [1.1.1]Propellane with electrophilic nitrogen-radicals
  publication-title: Angew. Chem. Int. Ed.
– volume: 145
  start-page: 25411
  year: 2023
  end-page: 25421
  ident: bib85
  article-title: Photocatalyzed [2σ + 2σ] and [2σ + 2π] cycloadditions for the synthesis of bicyclo[3.1.1]heptanes and 5- or 6-membered carbocycles
  publication-title: J. Am. Chem. Soc.
– volume: 59
  start-page: 6056
  year: 2023
  end-page: 6059
  ident: bib142
  article-title: Synthesis of C3-halo substituted bicyclo[1.1.1]pentylamines via halosulfoamidation of [1.1.1]propellane with sodium hypohalites and sulfonamides
  publication-title: Chem. Commun.
– volume: 92
  start-page: 751
  year: 2020
  end-page: 765
  ident: bib10
  article-title: Recent advances in the chemistry of bicyclo- and 1-azabicyclo[1.1.0]butanes
  publication-title: Pure Appl. Chem.
– volume: 59
  start-page: 7467
  year: 2023
  end-page: 7470
  ident: bib41
  article-title: Heteroannulation of bicyclobutane derivatives via Au-catalyzed hydration to enol ethers and intramolecular cyclization giving spirocyclobutanes
  publication-title: Chem. Commun.
– volume: 61
  year: 2022
  ident: bib69
  article-title: Diboron(4)-Catalyzed remote [3+2] cycloaddition of cyclopropanes via dearomative/rearomative radical transmission through pyridine
  publication-title: Angew. Chem. Int. Ed.
– volume: 22
  start-page: 6021
  year: 2020
  end-page: 6025
  ident: bib167
  article-title: Copper-catalyzed cross-coupling between alkyl (Pseudo)halides and bicyclopentyl grignard reagents
  publication-title: Org. Lett.
– volume: 49
  start-page: 5986
  year: 2008
  end-page: 5989
  ident: bib97
  article-title: Formal Alder-ene reaction of a bicyclo[1.1.0]butane in the synthesis of the tricyclic quaternary ammonium core of daphniglaucins
  publication-title: Tetrahedron Lett.
– volume: 16
  start-page: 2958
  year: 2014
  end-page: 2975
  ident: bib131
  article-title: Multicomponent reactions: advanced tools for sustainable organic synthesis
  publication-title: Green Chem.
– volume: 24
  start-page: 4292
  year: 2022
  end-page: 4297
  ident: bib155
  article-title: Radical acylation of [1.1.1]Propellane with aldehydes: synthesis of bicyclo[1.1.1]pentane ketones
  publication-title: Org. Lett.
– volume: 6
  start-page: 1589
  year: 2020
  end-page: 1603
  ident: bib76
  article-title: Shaping molecular landscapes: recent advances, opportunities, and challenges in dearomatization
  publication-title: Chem
– volume: 114
  start-page: 601
  year: 1992
  end-page: 620
  ident: bib120
  article-title: Toward a molecular-size tinkertoy construction set. Preparation of terminally functionalized [n]staffanes from [1.1.1]propellane
  publication-title: J. Am. Chem. Soc.
– volume: 59
  start-page: 2618
  year: 2020
  end-page: 2622
  ident: bib45
  article-title: Photochemical strain-release-driven cyclobutylation of C(sp
  publication-title: Angew. Chem. Int. Ed.
– volume: 23
  start-page: 3615
  year: 2021
  end-page: 3619
  ident: bib98
  article-title: Semipinacol-Type Rearrangements of [3-(Arylsulfonyl)bicyclo[1.1.0]butan-1-yl]alkanols
  publication-title: Org. Lett.
– volume: 24
  start-page: 7015
  year: 2022
  end-page: 7020
  ident: bib175
  article-title: Synthesis of sulfur-substituted bicyclo[1.1.1]pentanes by iodo-sulfenylation of [1.1.1]Propellane, org
  publication-title: Letture
– volume: 58
  start-page: 13416
  year: 2019
  end-page: 13420
  ident: bib173
  article-title: Reactions of 2-aryl-1,3-dithianes and [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
– volume: 53
  start-page: 4593
  year: 1988
  end-page: 4594
  ident: bib118
  article-title: A practical photochemical synthesis of bicyclo[1.1.1]pentane-1,3-dicarboxylic acid
  publication-title: J. Org. Chem.
– volume: 134
  year: 2023
  ident: bib99
  article-title: Expedient synthesis of spiro[3.3]heptan-1-ones via strain-relocating semipinacol rearrangements
  publication-title: Tetrahedron
– volume: 8
  start-page: 43
  year: 2017
  end-page: 48
  ident: bib22
  article-title: Investigation of a bicyclo[1.1.1]pentane as a phenyl replacement within an LpPLA
  publication-title: ACS Med. Chem. Lett.
– volume: 62
  year: 2023
  ident: bib156
  article-title: Rapid and scalable halosulfonylation of strain-release reagents
  publication-title: Angew. Chem. Int. Ed.
– volume: 60
  start-page: 24754
  year: 2021
  end-page: 24769
  ident: bib115
  article-title: Bridge functionalisation of bicyclo[1.1.1]pentane derivatives
  publication-title: Angew. Chem. Int. Ed.
– volume: 17
  start-page: 3892
  year: 2015
  end-page: 3894
  ident: bib64
  article-title: Total synthesis of aquatolide
  publication-title: Org. Lett.
– volume: 18
  start-page: 3411
  year: 1977
  end-page: 3412
  ident: bib53
  article-title: Synthesis of 1,3-disubstituted bicyclo[1.1.1]pentanes
  publication-title: Tetrahedron Lett.
– volume: 57
  start-page: 8449
  year: 2021
  end-page: 8451
  ident: bib105
  article-title: Strain-release C–C bond cleavage enables the [2,3]-sigmatropic rearrangement of tertiary allylamines
  publication-title: Chem. Commun.
– volume: 62
  year: 2023
  ident: bib73
  article-title: Intermolecular formal cycloaddition of indoles with bicyclo[1.1.0]butanes by Lewis acid catalysis
  publication-title: Angew. Chem. Int. Ed.
– volume: 580
  start-page: 220
  year: 2020
  end-page: 226
  ident: bib134
  article-title: Copper-mediated synthesis of drug-like bicyclopentanes
  publication-title: Nature
– volume: 50
  start-page: 2943
  year: 1985
  end-page: 2947
  ident: bib28
  article-title: Stereochemistry of addition of organocopper reagents and of the hydride ion to 1-(arylsulfonyl)bicyclo[1.1.0]butanes
  publication-title: J. Org. Chem.
– volume: 135
  start-page: 9283
  year: 2013
  end-page: 9286
  ident: bib39
  article-title: Enantioselective synthesis of cyclobutanes via sequential Rh-catalyzed bicyclobutanation/Cu-catalyzed homoconjugate addition
  publication-title: J. Am. Chem. Soc.
– volume: 145
  start-page: 12324
  year: 2023
  end-page: 12332
  ident: bib78
  article-title: ortho-Selective dearomative [2π + 2σ] photocycloadditions of bicyclic aza-arenes
  publication-title: J. Am. Chem. Soc.
– volume: 59
  start-page: 20235
  year: 2020
  end-page: 20241
  ident: bib171
  article-title: Highly regioselective addition of allylic zinc halides and various zinc enolates to [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
– volume: 144
  start-page: 20875
  year: 2022
  end-page: 20883
  ident: bib111
  article-title: Palladium hydride-enabled hydroalkenylation of strained molecules
  publication-title: J. Am. Chem. Soc.
– volume: 62
  year: 2023
  ident: bib141
  article-title: A general and practical route to functionalized bicyclo[1.1.1]Pentane-heteroaryls enabled by photocatalytic multicomponent heteroarylation of [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
– volume: 143
  start-page: 9729
  year: 2021
  end-page: 9736
  ident: bib154
  article-title: Twofold radical-based synthesis of N,C-difunctionalized bicyclo[1.1.1]pentanes
  publication-title: J. Am. Chem. Soc.
– volume: 23
  start-page: 5215
  year: 1982
  end-page: 5218
  ident: bib26
  article-title: Conjugate addition of organocopper reagents to 1-arylsulfonylbicyclobutanes. synthesis of the racemic form of the sex pheromone of the citrus mealybug, Planococcus citri (Risso)
  publication-title: Tetrahedron Lett.
– volume: 51
  start-page: 2313
  year: 2022
  end-page: 2382
  ident: bib132
  article-title: Multicomponent reactions and photo/electrochemistry join forces: atom economy meets energy efficiency
  publication-title: Chem. Soc. Rev.
– volume: 13
  start-page: 5096
  year: 2023
  end-page: 5103
  ident: bib70
  article-title: Pyridine-boryl radical-catalyzed [2π + 2σ] cycloaddition of bicyclo[1.1.0]butanes with alkenes
  publication-title: ACS Catal.
– volume: 140
  start-page: 14836
  year: 2018
  end-page: 14843
  ident: bib43
  article-title: Ti-catalyzed radical alkylation of secondary and tertiary alkyl chlorides using michael acceptors
  publication-title: J. Am. Chem. Soc.
– volume: 100
  start-page: 169
  year: 2000
  end-page: 234
  ident: bib121
  article-title: Bicyclo[1.1.1]pentanes, [n]Staffanes, [1.1.1]Propellanes, and tricyclo[2.1.0.0
  publication-title: Chem. Rev.
– volume: 14
  start-page: 13060
  year: 2023
  end-page: 13066
  ident: bib50
  article-title: Photochemical α-selective radical ring-opening reactions of 1,3-disubstituted acyl bicyclobutanes with alkyl halides: modular access to functionalized cyclobutenes
  publication-title: Chem. Sci.
– volume: 142
  start-page: 18522
  year: 2020
  end-page: 18531
  ident: bib34
  article-title: Bicyclobutane carboxylic amide as a cysteine-directed strained electrophile for selective targeting of proteins
  publication-title: J. Am. Chem. Soc.
– volume: 24
  start-page: 6049
  year: 2022
  end-page: 6053
  ident: bib149
  article-title: Synthesis and biological evaluation of bicyclo[1.1.1]pentane-containing aromatic lipoxin A
  publication-title: Org. Lett.
– volume: 23
  start-page: 3179
  year: 2021
  end-page: 3183
  ident: bib169
  article-title: Enantioselective synthesis of bicyclopentane-containing alcohols via asymmetric transfer hydrogenation
  publication-title: Org. Lett.
– volume: 62
  year: 2023
  ident: bib87
  article-title: Lewis acid catalyzed formal (3+2)-cycloaddition of bicyclo[1.1.0]butanes with ketenes
  publication-title: Angew. Chem. Int. Ed.
– volume: 59
  start-page: 1970
  year: 2020
  end-page: 1974
  ident: bib153
  article-title: Silaboration of [1.1.1]Propellane: a storable feedstock for bicyclo[1.1.1]pentane derivatives
  publication-title: Angew. Chem. Int. Ed.
– volume: 21
  start-page: 7199
  year: 2019
  end-page: 7203
  ident: bib56
  article-title: A selective synthesis of 2,2-difluorobicyclo[1.1.1]pentane analogues: “BCP-F
  publication-title: Org. Lett.
– volume: 87
  start-page: 2393
  year: 2022
  end-page: 2401
  ident: bib168
  article-title: Synthesis and use of bicyclo[1.1.1]pentylaldehyde building blocks
  publication-title: J. Org. Chem.
– volume: 139
  start-page: 3209
  year: 2017
  end-page: 3226
  ident: bib32
  article-title: Strain-release heteroatom functionalization: development, scope, and stereospecificity
  publication-title: J. Am. Chem. Soc.
– volume: 23
  start-page: 8628
  year: 2021
  end-page: 8633
  ident: bib128
  article-title: Synthesis of α-quaternary bicyclo[1.1.1]pentanes through synergistic organophotoredox and hydrogen atom transfer catalysis
  publication-title: Org. Lett.
– year: 2024
  ident: bib52
  article-title: Strain-enabled radical spirocyclization cascades: rapid access to spirocyclobutyl lactones and – lactams
  publication-title: Chem. Sci.
– volume: 46
  start-page: 4090
  year: 1981
  end-page: 4092
  ident: bib82
  article-title: Bicyclo[1.1.0]butanes. Reactions with cyclic azo compounds
  publication-title: J. Org. Chem.
– volume: 60
  start-page: 7873
  year: 2021
  end-page: 7879
  ident: bib127
  article-title: Visible-light-induced 1,3-aminopyridylation of [1.1.1]Propellane with N-aminopyridinium salts
  publication-title: Angew. Chem. Int. Ed.
– volume: 29
  start-page: 467
  year: 2018
  end-page: 472
  ident: bib36
  article-title: Highly efficient and stable strain-release radioiodination for thiol chemoselective bioconjugation
  publication-title: Bioconjugate Chem.
– volume: 55
  start-page: 4983
  year: 2016
  end-page: 4987
  ident: bib40
  article-title: A mixed-ligand chiral rhodium(II) catalyst enables the enantioselective total synthesis of piperarborenine B
  publication-title: Angew. Chem. Int. Ed.
– volume: 143
  start-page: 21246
  year: 2021
  end-page: 21251
  ident: bib60
  article-title: Synthesis and applications of polysubstituted bicyclo[1.1.0]butanes
  publication-title: J. Am. Chem. Soc.
– volume: 12
  start-page: 7480
  year: 2021
  end-page: 7485
  ident: bib59
  article-title: Synthesis of 1,3-disubstituted bicyclo[1.1.0]butanes via directed bridgehead functionalization
  publication-title: Chem. Sci.
– volume: 145
  start-page: 24466
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib108
  article-title: Enantioselective, intermolecular [π2+σ2] photocycloaddition reactions of 2(1H)-Quinolones and bicyclo[1.1.0]butanes
  publication-title: J. Am. Chem. Soc.
– volume: 14
  start-page: 13060
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib50
  article-title: Photochemical α-selective radical ring-opening reactions of 1,3-disubstituted acyl bicyclobutanes with alkyl halides: modular access to functionalized cyclobutenes
  publication-title: Chem. Sci.
  doi: 10.1039/D3SC04457B
– volume: 24
  start-page: 1268
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib81
  article-title: Investigating bicyclobutane–triazolinedione cycloadditions as a tool for peptide modification
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.1c04071
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib93
  article-title: Catalytic formal [2π+2σ] cycloaddition of aldehydes with bicyclobutanes: expedient access to polysubstituted 2-oxabicyclo[2.1.1]hexanes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202305043
– volume: 145
  start-page: 25411
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib85
  article-title: Photocatalyzed [2σ + 2σ] and [2σ + 2π] cycloadditions for the synthesis of bicyclo[3.1.1]heptanes and 5- or 6-membered carbocycles
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c09789
– volume: 11
  start-page: 117
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib101
  article-title: Carbopalladation of C–C σ-bonds enabled by strained boronate complexes
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-018-0181-x
– volume: 15
  start-page: 419
  year: 2024
  ident: 10.1016/j.tchem.2024.100070_bib146
  article-title: C−F bond activation enables synthesis of aryl difluoromethyl bicyclopentanes as benzophenone-type bioisosteres
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-023-44653-6
– volume: 146
  start-page: 1196
  year: 2024
  ident: 10.1016/j.tchem.2024.100070_bib42
  article-title: Stereoselective alder-ene reactions of bicyclo[1.1.0]butanes: facile synthesis of cyclopropyl- and aryl-substituted cyclobutenes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c13080
– volume: 59
  start-page: 1970
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib153
  article-title: Silaboration of [1.1.1]Propellane: a storable feedstock for bicyclo[1.1.1]pentane derivatives
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201909655
– volume: 59
  start-page: 7467
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib41
  article-title: Heteroannulation of bicyclobutane derivatives via Au-catalyzed hydration to enol ethers and intramolecular cyclization giving spirocyclobutanes
  publication-title: Chem. Commun.
  doi: 10.1039/D3CC01955A
– volume: 55
  start-page: 14976
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib150
  article-title: A radical exchange process: synthesis of bicyclo[1.1.1]pentane derivatives of xanthates
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC07610G
– volume: 58
  start-page: 13416
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib173
  article-title: Reactions of 2-aryl-1,3-dithianes and [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201905531
– volume: 25
  start-page: 4590
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib8
  article-title: Nonconjugated hydrocarbons as rigid-linear motifs: isosteres for material sciences and bioorganic and medicinal chemistry
  publication-title: Chem. Eur J.
  doi: 10.1002/chem.201804225
– volume: 9
  start-page: 2234
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib160
  article-title: Synthesis of tetrasubstituted alkenyl nitriles via cyanocarbene addition of [1.1.1]propellane
  publication-title: Org. Chem. Front.
  doi: 10.1039/D2QO00186A
– volume: 364
  start-page: 2140
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib47
  article-title: Transition metal-free radical α-oxy C−H cyclobutylation via photoinduced hydrogen atom transfer
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.202200281
– volume: 17
  start-page: 2839
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib62
  article-title: Saturated bioisosteres of benzene: where to go next?
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C8OB02812E
– volume: 17
  start-page: 3892
  year: 2015
  ident: 10.1016/j.tchem.2024.100070_bib64
  article-title: Total synthesis of aquatolide
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b01888
– volume: 14
  start-page: 1068
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib139
  article-title: Exploiting the sp2 character of bicyclo[1.1.1]pentyl radicals in the transition-metal-free multi-component difunctionalization of [1.1.1]propellane
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-022-00979-0
– volume: 21
  start-page: 6800
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib170
  article-title: Aminoalkylation of [1.1.1]Propellane enables direct access to high-value 3-Alkylbicyclo[1.1.1]pentan-1-amines
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b02426
– volume: 24
  start-page: 7015
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib175
  article-title: Synthesis of sulfur-substituted bicyclo[1.1.1]pentanes by iodo-sulfenylation of [1.1.1]Propellane, org
  publication-title: Letture
– volume: 351
  start-page: 241
  year: 2016
  ident: 10.1016/j.tchem.2024.100070_bib5
  article-title: Strain-release amination
  publication-title: Science
  doi: 10.1126/science.aad6252
– volume: 51
  start-page: 2145
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib77
  article-title: Visible-light induced dearomatization reactions
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00311H
– volume: 25
  start-page: 312
  year: 1986
  ident: 10.1016/j.tchem.2024.100070_bib15
  article-title: The concept of strain in organic chemistry
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.198603121
– volume: 145
  start-page: 12324
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib78
  article-title: ortho-Selective dearomative [2π + 2σ] photocycloadditions of bicyclic aza-arenes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c02961
– volume: 60
  start-page: 212
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib104
  article-title: α-Selective ring-opening reactions of bicyclo[1.1.0]butyl boronic ester with nucleophiles
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202011739
– volume: 15
  start-page: 535
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib71
  article-title: A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-023-01135-y
– volume: 56
  start-page: 5684
  year: 2017
  ident: 10.1016/j.tchem.2024.100070_bib6
  article-title: Propellanes—from a chemical curiosity to “explosive” materials and natural products
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201603951
– volume: 13
  start-page: 5096
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib70
  article-title: Pyridine-boryl radical-catalyzed [2π + 2σ] cycloaddition of bicyclo[1.1.0]butanes with alkenes
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.3c00305
– volume: 87
  start-page: 2393
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib168
  article-title: Synthesis and use of bicyclo[1.1.1]pentylaldehyde building blocks
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.1c02267
– volume: 9
  start-page: 2149
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib80
  article-title: Diastereoselective synthesis of 1,1,3,3-tetrasubstituted cyclobutanes enabled by cycloaddition of bicyclo[1.1.0]butanes
  publication-title: Org. Chem. Front.
  doi: 10.1039/D2QO00167E
– volume: 55
  start-page: 4983
  year: 2016
  ident: 10.1016/j.tchem.2024.100070_bib40
  article-title: A mixed-ligand chiral rhodium(II) catalyst enables the enantioselective total synthesis of piperarborenine B
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201600766
– volume: 59
  start-page: 2618
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib45
  article-title: Photochemical strain-release-driven cyclobutylation of C(sp3)-Centered radicals
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201908951
– volume: 15
  start-page: 1172
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib125
  article-title: Insertion of [1.1.1]propellane into aromatic disulfides
  publication-title: Beilstein J. Org. Chem.
  doi: 10.3762/bjoc.15.114
– volume: 50
  start-page: 2943
  year: 1985
  ident: 10.1016/j.tchem.2024.100070_bib28
  article-title: Stereochemistry of addition of organocopper reagents and of the hydride ion to 1-(arylsulfonyl)bicyclo[1.1.0]butanes
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00216a027
– volume: 56
  start-page: 307
  year: 1991
  ident: 10.1016/j.tchem.2024.100070_bib117
  article-title: Synthesis of doubly bridgehead substituted bicyclo[1.1.1]pentanes. Radical transformations of bridgehead halides and carboxylic acids
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00001a058
– volume: 14
  start-page: 6585
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib37
  article-title: Lewis acid-catalyzed diastereoselective carbofunctionalization of bicyclobutanes employing naphthols
  publication-title: Chem. Sci.
  doi: 10.1039/D3SC01373A
– volume: 143
  start-page: 7648
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib110
  article-title: Use of strain-release for the diastereoselective construction of quaternary carbon centers
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.1c03492
– volume: 139
  start-page: 3209
  year: 2017
  ident: 10.1016/j.tchem.2024.100070_bib32
  article-title: Strain-release heteroatom functionalization: development, scope, and stereospecificity
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b13229
– volume: 60
  start-page: 675
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib46
  article-title: Oligosilanes as silyl radical precursors through oxidative Si−Si bond cleavage using redox catalysis
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202011738
– volume: 46
  start-page: 4090
  year: 1981
  ident: 10.1016/j.tchem.2024.100070_bib82
  article-title: Bicyclo[1.1.0]butanes. Reactions with cyclic azo compounds
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00333a039
– volume: 13
  start-page: 13325
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib162
  article-title: Three-component cyclobutylation via silver(I)-Catalyzed carbene transfer reactions with [1.1.1]Propellane
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.3c03681
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib100
  article-title: Strain-release driven epoxidation and aziridination of bicyclo[1.1.0]butanes via palladium catalyzed σ-bond nucleopalladation
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202217064
– volume: 76
  start-page: 461
  year: 1976
  ident: 10.1016/j.tchem.2024.100070_bib3
  article-title: Transition metal catalyzed rearrangements of small ring organic molecules
  publication-title: Chem. Rev.
  doi: 10.1021/cr60302a003
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib141
  article-title: A general and practical route to functionalized bicyclo[1.1.1]Pentane-heteroaryls enabled by photocatalytic multicomponent heteroarylation of [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
– volume: 12
  start-page: 9262
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib94
  article-title: Recent development and applications of semipinacol rearrangement reactions
  publication-title: Chem. Sci.
  doi: 10.1039/D1SC02386A
– volume: 9
  start-page: 5295
  year: 2018
  ident: 10.1016/j.tchem.2024.100070_bib148
  article-title: Synthesis and applications of highly functionalized 1-halo-3-substituted bicyclo[1.1.1]pentanes
  publication-title: Chem. Sci.
  doi: 10.1039/C8SC01355A
– volume: 142
  start-page: 16766
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib103
  article-title: Difunctionalization of C–C σ-bonds enabled by the reaction of bicyclo[1.1.0]butyl boronate complexes with electrophiles: reaction development, scope, and stereochemical origins
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c07357
– volume: 18
  start-page: 2269
  year: 1885
  ident: 10.1016/j.tchem.2024.100070_bib1
  article-title: Ueber polyacetylenverbindungen
  publication-title: Ber. Dtsch. Chem. Ges.
  doi: 10.1002/cber.18850180296
– year: 2024
  ident: 10.1016/j.tchem.2024.100070_bib52
  article-title: Strain-enabled radical spirocyclization cascades: rapid access to spirocyclobutyl lactones and – lactams
  publication-title: Chem. Sci.
  doi: 10.1039/D3SC05700C
– volume: 46
  start-page: 4092
  year: 1981
  ident: 10.1016/j.tchem.2024.100070_bib83
  article-title: 2,3-Diazabicyclo[2.1.1]hex-2-ene. Synthesis and thermal decomposition
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00333a040
– volume: 100
  start-page: 169
  year: 2000
  ident: 10.1016/j.tchem.2024.100070_bib121
  article-title: Bicyclo[1.1.1]pentanes, [n]Staffanes, [1.1.1]Propellanes, and tricyclo[2.1.0.02,5]pentanes
  publication-title: Chem. Rev.
  doi: 10.1021/cr990094z
– volume: 24
  start-page: 4609
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib136
  article-title: Radical multicomponent alkyl alkynylation of propellane via synergistic photoredox and copper catalysis
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.2c01721
– volume: 10
  start-page: 4616
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib143
  article-title: Photocatalyzed radical multicomponent alkylacylation of [1.1.1]propellane to synthesize 1,3-disubstituted BCP ketones
  publication-title: Org. Chem. Front.
  doi: 10.1039/D3QO01019H
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib73
  article-title: Intermolecular formal cycloaddition of indoles with bicyclo[1.1.0]butanes by Lewis acid catalysis
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202308606
– volume: 142
  start-page: 18522
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib34
  article-title: Bicyclobutane carboxylic amide as a cysteine-directed strained electrophile for selective targeting of proteins
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c07490
– volume: 141
  start-page: 9511
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib102
  article-title: Radical addition to strained σ-bonds enables the stereocontrolled synthesis of cyclobutyl boronic esters
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b03653
– volume: 63
  start-page: 1025
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib151
  article-title: A practical access to fluoroalkylthio(seleno)-functionalized bicyclo[1.1.1]pentanes
  publication-title: Sci. China Chem.
  doi: 10.1007/s11426-020-9733-y
– volume: 29
  start-page: 1591
  year: 1988
  ident: 10.1016/j.tchem.2024.100070_bib30
  article-title: Regiospecific additions of hydrazoic acid and benzylamine to 1-(arylsulfonyl)bicyclo[1.1.0]Butanes. Application to the synthesis of cis and trans 2,7-methanoglutamic acids
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(00)80361-5
– volume: 143
  start-page: 21246
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib60
  article-title: Synthesis and applications of polysubstituted bicyclo[1.1.0]butanes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.1c11244
– volume: 2020
  start-page: 4581
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib57
  article-title: Synthetic studies of 2,2-difluorobicyclo[1.1.1]pentanes (BCP-F2): the scope and limitation of useful building blocks for medicinal chemists
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.202000679
– volume: 31
  start-page: 3065
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib114
  article-title: Recent advances in the applications of [1.1.1]propellane in organic synthesis, Chin
  publication-title: Chem. Lett.
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib156
  article-title: Rapid and scalable halosulfonylation of strain-release reagents
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202213508
– volume: 60
  start-page: 7873
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib127
  article-title: Visible-light-induced 1,3-aminopyridylation of [1.1.1]Propellane with N-aminopyridinium salts
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202016156
– volume: 50
  start-page: 11577
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib95
  article-title: Radical-mediated rearrangements: past, present, and future
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/D1CS00529D
– volume: 59
  start-page: 6056
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib142
  article-title: Synthesis of C3-halo substituted bicyclo[1.1.1]pentylamines via halosulfoamidation of [1.1.1]propellane with sodium hypohalites and sulfonamides
  publication-title: Chem. Commun.
  doi: 10.1039/D3CC01262J
– volume: 30
  start-page: 1
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib7
  article-title: Recent advances in the synthetic chemistry of bicyclo[1.1.1]pentane
  publication-title: Synlett
  doi: 10.1055/s-0037-1610314
– volume: 145
  start-page: 4304
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib84
  article-title: Selective [2σ + 2σ] cycloaddition enabled by boronyl radical catalysis: synthesis of highly substituted bicyclo[3.1.1]heptanes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c13740
– volume: 23
  start-page: 5219
  year: 1982
  ident: 10.1016/j.tchem.2024.100070_bib25
  article-title: Aryl cyclobutyl sulfones by reduction of 1-arylsulfonylbicyclobutanes with lithium aluminium hydride. synthesis of racemic junionone
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(00)85802-5
– volume: 47
  start-page: 4985
  year: 1982
  ident: 10.1016/j.tchem.2024.100070_bib54
  article-title: Polar substituent effects in 1,3-disubstituted bicyclo[1.1.1]pentanes
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00146a031
– volume: 12
  start-page: 590
  year: 2017
  ident: 10.1016/j.tchem.2024.100070_bib23
  article-title: Improving nonspecific binding and solubility: bicycloalkyl groups and cubanes as para-phenyl bioisosteres
  publication-title: ChemMedChem
  doi: 10.1002/cmdc.201700082
– volume: 1999
  start-page: 2079
  year: 1999
  ident: 10.1016/j.tchem.2024.100070_bib163
  article-title: A facile route to bridgehead disubstituted bicyclo[1.1.1]pentanes involving palladium-catalyzed cross-coupling reactions
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/(SICI)1099-0690(199909)1999:9<2079::AID-EJOC2079>3.0.CO;2-D
– volume: 13
  start-page: 11721
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib12
  article-title: Bicyclobutanes: from curiosities to versatile reagents and covalent warheads
  publication-title: Chem. Sci.
  doi: 10.1039/D2SC03948F
– volume: 140
  start-page: 14836
  year: 2018
  ident: 10.1016/j.tchem.2024.100070_bib43
  article-title: Ti-catalyzed radical alkylation of secondary and tertiary alkyl chlorides using michael acceptors
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b08605
– volume: 59
  start-page: 20515
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib63
  article-title: Saturated bioisosteres of ortho-substituted benzenes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202004183
– volume: 24
  start-page: 4292
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib155
  article-title: Radical acylation of [1.1.1]Propellane with aldehydes: synthesis of bicyclo[1.1.1]pentane ketones
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.2c01707
– volume: 145
  start-page: 23771
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib49
  article-title: syn-Selective difunctionalization of bicyclobutanes enabled by photoredox-mediated C–S σ-bond scission
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c08512
– volume: 15
  start-page: 1155
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib91
  article-title: 2-Oxabicyclo[2.1.1]hexanes as saturated bioisosteres of the ortho-substituted phenyl ring
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-023-01222-0
– volume: 59
  start-page: 3917
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib166
  article-title: 1,3-Difunctionalizations of [1.1.1]Propellane via 1,2-metallate rearrangements of boronate complexes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201914875
– volume: 56
  start-page: 5718
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib11
  article-title: Strain release–an old tool for new transformations
  publication-title: Chem. Commun.
  doi: 10.1039/D0CC01771J
– volume: 27
  start-page: 185
  year: 1995
  ident: 10.1016/j.tchem.2024.100070_bib31
  article-title: Synthesis of AMINOCYCLOBUTANE mono- and dicarboxylic acids and derivatives thereof from (PHENYLSULFONYL)BICYCLOBUTANES
  publication-title: Org. Prep. Proced. Int.
  doi: 10.1080/00304949509458453
– volume: 61
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib69
  article-title: Diboron(4)-Catalyzed remote [3+2] cycloaddition of cyclopropanes via dearomative/rearomative radical transmission through pyridine
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202214507
– volume: 14
  start-page: 619
  year: 2024
  ident: 10.1016/j.tchem.2024.100070_bib144
  article-title: General and modular route to (Halo)alkyl BCP-heteroaryls enabled by α-aminoalkyl radical-mediated halogen-atom transfer
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.3c05003
– volume: 26
  start-page: 2808
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib35
  article-title: Structurally diverse acyl bicyclobutanes: valuable strained electrophiles
  publication-title: Chem. Eur J.
  doi: 10.1002/chem.201905539
– volume: 45
  start-page: 4172
  year: 2006
  ident: 10.1016/j.tchem.2024.100070_bib66
  article-title: Pericyclic cascade reactions of (Bicyclo[1.1.0]butylmethyl)amines
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.200600723
– volume: 144
  start-page: 12961
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib137
  article-title: Dicarbofunctionalization of [1.1.1]Propellane enabled by nickel/photoredox dual catalysis: one-step multicomponent strategy for the synthesis of BCP-aryl derivatives
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c05304
– volume: 24
  start-page: 8821
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib65
  article-title: Bicyclo[2.1.1]hexanes by visible light-driven intramolecular crossed [2 + 2] photocycloadditions, org
  publication-title: Letture
– volume: 605
  start-page: 477
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib67
  article-title: Intermolecular [2π+2σ]-photocycloaddition enabled by triplet energy transfer
  publication-title: Nature
  doi: 10.1038/s41586-022-04636-x
– volume: 8
  start-page: 43
  year: 2017
  ident: 10.1016/j.tchem.2024.100070_bib22
  article-title: Investigation of a bicyclo[1.1.1]pentane as a phenyl replacement within an LpPLA2 inhibitor
  publication-title: ACS Med. Chem. Lett.
  doi: 10.1021/acsmedchemlett.6b00281
– volume: 29
  start-page: 467
  year: 2018
  ident: 10.1016/j.tchem.2024.100070_bib36
  article-title: Highly efficient and stable strain-release radioiodination for thiol chemoselective bioconjugation
  publication-title: Bioconjugate Chem.
  doi: 10.1021/acs.bioconjchem.7b00790
– volume: 50
  start-page: 2948
  year: 1985
  ident: 10.1016/j.tchem.2024.100070_bib29
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00216a028
– volume: 21
  start-page: 7666
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib113
  article-title: Synthesis of 1,3-disubstituted bicyclo[1.1.1]pentanes by cross-coupling induced by transition metals–formation of C–C bonds, Org
  publication-title: Biomol. Chem.
  doi: 10.1039/D3OB01036H
– volume: 144
  start-page: 20207
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib92
  article-title: Synthesis of polysubstituted 2-oxabicyclo[2.1.1]hexanes via visible-light-induced energy transfer
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c09248
– volume: 145
  start-page: 20716
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib124
  article-title: Strain-release photocatalysis
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c08206
– volume: 31
  start-page: 51
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib44
  article-title: Radical α-C–H cyclobutylation of aniline derivatives
  publication-title: Synlett
  doi: 10.1055/s-0039-1690197
– volume: 144
  start-page: 7988
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib68
  article-title: Strain-release [2π + 2σ] cycloadditions for the synthesis of bicyclo[2.1.1]hexanes initiated by energy transfer
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c02976
– volume: 51
  start-page: 2313
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib132
  article-title: Multicomponent reactions and photo/electrochemistry join forces: atom economy meets energy efficiency
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/D1CS00510C
– volume: 55
  start-page: 3414
  year: 2012
  ident: 10.1016/j.tchem.2024.100070_bib21
  article-title: Application of the bicyclo[1.1.1]pentane motif as a nonclassical phenyl ring bioisostere in the design of a potent and orally active γ-secretase inhibitor
  publication-title: J. Med. Chem.
  doi: 10.1021/jm300094u
– volume: 56
  start-page: 12774
  year: 2017
  ident: 10.1016/j.tchem.2024.100070_bib165
  article-title: Synthesis of bicyclo[1.1.1]pentane bioisosteres of internal alkynes and para-disubstituted benzenes from [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201706799
– volume: 21
  start-page: 10057
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib158
  article-title: Copper-catalyzed ring opening of [1.1.1]Propellane with alkynes: synthesis of exocyclic allenic cyclobutanes
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b03999
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib87
  article-title: Lewis acid catalyzed formal (3+2)-cycloaddition of bicyclo[1.1.0]butanes with ketenes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202304771
– volume: 18
  start-page: 3411
  year: 1977
  ident: 10.1016/j.tchem.2024.100070_bib53
  article-title: Synthesis of 1,3-disubstituted bicyclo[1.1.1]pentanes
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(01)83253-6
– volume: 381
  start-page: 75
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib112
  article-title: Dearomative ring expansion of thiophenes by bicyclobutane insertion
  publication-title: Science
  doi: 10.1126/science.adh9737
– volume: 2000
  start-page: 1137
  year: 2000
  ident: 10.1016/j.tchem.2024.100070_bib164
  article-title: Nickel- and palladium-catalyzed cross-coupling reactions at the bridgehead of bicyclo[1.1.1]pentane derivatives - a convenient access to liquid crystalline compounds containing bicyclo[1.1.1]pentane moieties
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/1099-0690(200004)2000:7<1137::AID-EJOC1137>3.0.CO;2-2
– volume: 12
  start-page: 14507
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib106
  article-title: Skeletal ring contractions via I(I)/I(III) catalysis: stereoselective synthesis of cis-α,α-Difluorocyclopropanes
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.2c04511
– volume: 75
  start-page: 98
  year: 1998
  ident: 10.1016/j.tchem.2024.100070_bib24
  article-title: [1.1.1]propellane, Org
  publication-title: Synth. Met.
– volume: 139
  start-page: 17791
  year: 2017
  ident: 10.1016/j.tchem.2024.100070_bib133
  article-title: Radical multicomponent carboamination of [1.1.1]Propellane
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b11865
– volume: 18
  start-page: 4300
  year: 2016
  ident: 10.1016/j.tchem.2024.100070_bib33
  article-title: Hydrophosphination of bicyclo[1.1.0]butane-1-carbonitriles
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.6b02051
– volume: 116
  start-page: 9816
  year: 2016
  ident: 10.1016/j.tchem.2024.100070_bib75
  article-title: Arene–Alkene cycloaddition
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.6b00005
– volume: 145
  start-page: 21152
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib107
  article-title: Enantioselective synthesis of chiral cyclobutenes enabled by brønsted acid-catalyzed isomerization of BCBs
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c06525
– volume: 144
  start-page: 23685
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib88
  article-title: Photochemical intermolecular [3σ + 2σ]-cycloaddition for the construction of aminobicyclo[3.1.1]heptanes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c11501
– volume: 144
  start-page: 20875
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib111
  article-title: Palladium hydride-enabled hydroalkenylation of strained molecules
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c09045
– volume: 23
  start-page: 3179
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib169
  article-title: Enantioselective synthesis of bicyclopentane-containing alcohols via asymmetric transfer hydrogenation
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.1c00889
– volume: 41
  start-page: 1453
  year: 1985
  ident: 10.1016/j.tchem.2024.100070_bib55
  article-title: Reactions of carbenes with bicyclobutanes and quadricyclane: cycloadditions with two σ bonds
  publication-title: Tetrahedron
  doi: 10.1016/S0040-4020(01)96386-0
– volume: 111
  start-page: 3750
  year: 1989
  ident: 10.1016/j.tchem.2024.100070_bib116
  article-title: Kinetics and mechanism of the reaction of diphenylcarbene with [1.1.1]propellane
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00192a043
– volume: 9
  start-page: 8
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib9
  article-title: Selected topics in the syntheses of bicyclo[1.1.1]Pentane (BCP) analogues
  publication-title: Asian J. Org. Chem.
  doi: 10.1002/ajoc.201900589
– volume: 37
  start-page: 1827
  year: 1988
  ident: 10.1016/j.tchem.2024.100070_bib17
  article-title: Molecular-mechanical analysis of the structure of strained organic molecules. 6. [m.n.k]-Propellanes
  publication-title: Bull. Acad. Sci. USSR, Div. Chem. Sci.
  doi: 10.1007/BF00962498
– volume: 130
  start-page: 6924
  year: 2008
  ident: 10.1016/j.tchem.2024.100070_bib96
  article-title: Rhodium(I)-Catalyzed cycloisomerizations of bicyclobutanes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja802906k
– volume: 7
  start-page: 2531
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib123
  article-title: Photoinduced strategies towards strained molecules
  publication-title: Org. Chem. Front.
  doi: 10.1039/D0QO00460J
– volume: 92
  start-page: 751
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib10
  article-title: Recent advances in the chemistry of bicyclo- and 1-azabicyclo[1.1.0]butanes
  publication-title: Pure Appl. Chem.
  doi: 10.1515/pac-2019-1007
– volume: 45
  start-page: 2819
  year: 1989
  ident: 10.1016/j.tchem.2024.100070_bib27
  article-title: New bridgehead-substituted 1-(arylsulfonyl)bicyclo[1.1.0]butanes and some novel addition reactions of the bicyclic system
  publication-title: Tetrahedron
  doi: 10.1016/S0040-4020(01)80112-5
– volume: 13
  start-page: 11936
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib138
  article-title: One step synthesis of unsymmetrical 1,3-disubstituted BCP ketones via nickel/photoredox-catalyzed [1.1.1]propellane multicomponent dicarbofunctionalization
  publication-title: Chem. Sci.
  doi: 10.1039/D2SC05100A
– volume: 34
  start-page: 558
  year: 2013
  ident: 10.1016/j.tchem.2024.100070_bib20
  article-title: Conventional strain energies of azetidine and phosphetane: can density functional theory yield reliable results?
  publication-title: J. Comput. Chem.
  doi: 10.1002/jcc.23165
– volume: 25
  start-page: 6184
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib48
  article-title: 2-Isopropylthioxanthone-Catalyzed divergent functionalization of bicyclo[1.1.0]butanes under visible-light irradiation
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.3c02332
– volume: 49
  start-page: 5986
  year: 2008
  ident: 10.1016/j.tchem.2024.100070_bib97
  article-title: Formal Alder-ene reaction of a bicyclo[1.1.0]butane in the synthesis of the tricyclic quaternary ammonium core of daphniglaucins
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2008.07.179
– volume: 61
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib86
  article-title: Beyond bioisosteres: divergent synthesis of azabicyclohexanes and cyclobutenyl amines from bicyclobutanes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202204719
– volume: 24
  start-page: 1373
  year: 2018
  ident: 10.1016/j.tchem.2024.100070_bib147
  article-title: Alkyl and aryl thiol addition to [1.1.1]Propellane: scope and limitations of a fast conjugation reaction
  publication-title: Chem. Eur J.
  doi: 10.1002/chem.201704105
– volume: 141
  start-page: 20325
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib159
  article-title: Methylenespiro[2.3]hexanes via nickel-catalyzed cyclopropanations with [1.1.1]Propellane
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b10689
– volume: 55
  start-page: 3
  year: 1990
  ident: 10.1016/j.tchem.2024.100070_bib119
  article-title: Stereoselective construction of the taxinine AB system through a novel tandem aldol-Payne rearrangement annulation
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00288a002
– volume: 57
  start-page: 15857
  year: 2018
  ident: 10.1016/j.tchem.2024.100070_bib172
  article-title: Synthesis of BCP benzylamines from 2-azaallyl anions and [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201810061
– volume: 142
  start-page: 5355
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib51
  article-title: Polarity-reversal strategy for the functionalization of electrophilic strained molecules via light-driven cobalt catalysis
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c00245
– volume: 24
  start-page: 6049
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib149
  article-title: Synthesis and biological evaluation of bicyclo[1.1.1]pentane-containing aromatic lipoxin A4 analogues
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.2c02345
– year: 2024
  ident: 10.1016/j.tchem.2024.100070_bib89
– volume: 60
  start-page: 24754
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib115
  article-title: Bridge functionalisation of bicyclo[1.1.1]pentane derivatives
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202106352
– volume: 59
  start-page: 8225
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib135
  article-title: Divergent strain-release amino-functionalization of [1.1.1]Propellane with electrophilic nitrogen-radicals
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202000140
– volume: 59
  start-page: 7161
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib90
  article-title: Water-soluble non-classical benzene mimetics
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202000548
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib130
  article-title: Access to polysulfides through photocatalyzed dithiosulfonylation
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202302199
– volume: 16
  start-page: 2958
  year: 2014
  ident: 10.1016/j.tchem.2024.100070_bib131
  article-title: Multicomponent reactions: advanced tools for sustainable organic synthesis
  publication-title: Green Chem.
  doi: 10.1039/C4GC00013G
– volume: 21
  start-page: 2749
  year: 1965
  ident: 10.1016/j.tchem.2024.100070_bib2
  article-title: Bicyclo[1.1.0]butane
  publication-title: Tetrahedron
  doi: 10.1016/S0040-4020(01)98361-9
– volume: 61
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib129
  article-title: Strain-release pentafluorosulfanylation and tetrafluoro(aryl)sulfanylation of [1.1.1]Propellane: reactivity and structural insight
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202211892
– volume: 25
  start-page: 8116
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib72
  article-title: Hantzsch esters enabled [2π+2σ] cycloadditions of bicyclo [1.1.0] butanes and alkenes under photo conditions
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.3c03222
– volume: 580
  start-page: 220
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib134
  article-title: Copper-mediated synthesis of drug-like bicyclopentanes
  publication-title: Nature
  doi: 10.1038/s41586-020-2060-z
– volume: 6
  start-page: 9
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib13
  article-title: Bicyclobutanes as unusual building blocks for complexity generation in organic synthesis
  publication-title: Commun. Chem.
  doi: 10.1038/s42004-022-00811-3
– volume: 28
  start-page: 411
  year: 1996
  ident: 10.1016/j.tchem.2024.100070_bib122
  article-title: Synthesis of biudgehead-substttuted bicyclo[1.1.1]pentanes
  publication-title: A Review, Org. Prep. Proced. Int.
  doi: 10.1080/00304949609356550
– volume: 25
  start-page: 5308
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib145
  article-title: Metal-free photoredox four-component strategy to 1,3-functionalized BCP derivatives
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.3c01877
– volume: 57
  start-page: 8449
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib105
  article-title: Strain-release C–C bond cleavage enables the [2,3]-sigmatropic rearrangement of tertiary allylamines
  publication-title: Chem. Commun.
  doi: 10.1039/D1CC03141D
– volume: 40
  start-page: 3431
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib152
  article-title: Radical-mediated bromoalkylation of [1.1.1]propellane: synthesis of bromo-substituted bicyclo[1.1.1]pentane derivatives, chin
  publication-title: J. Org. Chem.
– volume: 12
  start-page: 7066
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib174
  article-title: Strain-release 2-azaallyl anion addition/borylation of [1.1.1]propellane: synthesis and functionalization of benzylamine bicyclo[1.1.1]pentyl boronates
  publication-title: Chem. Sci.
  doi: 10.1039/D1SC01349A
– volume: 6
  start-page: 1589
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib76
  article-title: Shaping molecular landscapes: recent advances, opportunities, and challenges in dearomatization
  publication-title: Chem
  doi: 10.1016/j.chempr.2020.06.015
– volume: 230
  start-page: 387
  year: 1994
  ident: 10.1016/j.tchem.2024.100070_bib18
  article-title: Theoretical study of the 1J(13C13C) indirect nuclear spin-spin coupling constant of the bridgehead bond in [1.1.1]propellane and related systems
  publication-title: Chem. Phys. Lett.
  doi: 10.1016/0009-2614(94)01174-5
– volume: 62
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib74
  article-title: Silver-catalyzed dearomative [2π+2σ] cycloadditions of indoles with bicyclobutanes: access to indoline fused bicyclo[2.1.1]hexanes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202310066
– volume: 23
  start-page: 5215
  year: 1982
  ident: 10.1016/j.tchem.2024.100070_bib26
  article-title: Conjugate addition of organocopper reagents to 1-arylsulfonylbicyclobutanes. synthesis of the racemic form of the sex pheromone of the citrus mealybug, Planococcus citri (Risso)
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(00)85801-3
– volume: 23
  start-page: 3615
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib98
  article-title: Semipinacol-Type Rearrangements of [3-(Arylsulfonyl)bicyclo[1.1.0]butan-1-yl]alkanols
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.1c01004
– volume: 60
  start-page: 8103
  year: 2004
  ident: 10.1016/j.tchem.2024.100070_bib16
  article-title: Ring strain energies: substituted rings, norbornanes, norbornenes and norbornadienes
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2004.06.100
– volume: 61
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib176
  article-title: Electrophilic activation of [1.1.1]Propellane for the synthesis of nitrogen-substituted bicyclo[1.1.1]pentanes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202111291
– volume: 59
  start-page: 20235
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib171
  article-title: Highly regioselective addition of allylic zinc halides and various zinc enolates to [1.1.1]Propellane
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202009340
– volume: 143
  start-page: 9729
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib154
  article-title: Twofold radical-based synthesis of N,C-difunctionalized bicyclo[1.1.1]pentanes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.1c04180
– volume: 145
  start-page: 16508
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib109
  article-title: Iridium-catalyzed asymmetric difunctionalization of C–C σ-bonds enabled by ring-strained boronate complexes
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c03248
– volume: 4
  start-page: 81
  year: 1971
  ident: 10.1016/j.tchem.2024.100070_bib14
  article-title: Nuclear magnetic resonance spectra in liquid crystals and molecular structure
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar50039a001
– volume: 112
  start-page: 2194
  year: 1990
  ident: 10.1016/j.tchem.2024.100070_bib157
  article-title: Reactions of [1.1.1]propellane
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00162a022
– volume: 9
  start-page: 9568
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib126
  article-title: A general route to bicyclo[1.1.1]pentanes through photoredox catalysis
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b03190
– volume: 23
  start-page: 8628
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib128
  article-title: Synthesis of α-quaternary bicyclo[1.1.1]pentanes through synergistic organophotoredox and hydrogen atom transfer catalysis
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.1c03346
– volume: 48
  start-page: 1149
  year: 2015
  ident: 10.1016/j.tchem.2024.100070_bib4
  article-title: Ring-strain-enabled reaction discovery: new heterocycles from bicyclo[1.1.0]butanes
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar500437h
– volume: 53
  start-page: 4593
  year: 1988
  ident: 10.1016/j.tchem.2024.100070_bib118
  article-title: A practical photochemical synthesis of bicyclo[1.1.1]pentane-1,3-dicarboxylic acid
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00254a038
– volume: 21
  start-page: 7199
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib56
  article-title: A selective synthesis of 2,2-difluorobicyclo[1.1.1]pentane analogues: “BCP-F2”
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b02026
– volume: 134
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib99
  article-title: Expedient synthesis of spiro[3.3]heptan-1-ones via strain-relocating semipinacol rearrangements
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2023.133296
– volume: 14
  start-page: 9696
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib38
  article-title: C(sp2)–H cyclobutylation of hydroxyarenes enabled by silver-π-acid catalysis: diastereocontrolled synthesis of 1,3-difunctionalized cyclobutanes
  publication-title: Chem. Sci.
  doi: 10.1039/D3SC03258B
– volume: 61
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib61
  article-title: A practical and scalable approach to fluoro-substituted bicyclo[1.1.1]pentanes
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202205103
– year: 2024
  ident: 10.1016/j.tchem.2024.100070_bib79
  article-title: Photoredox-enabled dearomative [2π + 2σ] cycloaddition of phenols
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.3c12894
– volume: 135
  start-page: 9283
  year: 2013
  ident: 10.1016/j.tchem.2024.100070_bib39
  article-title: Enantioselective synthesis of cyclobutanes via sequential Rh-catalyzed bicyclobutanation/Cu-catalyzed homoconjugate addition
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja403811t
– volume: 24
  start-page: 7323
  year: 2022
  ident: 10.1016/j.tchem.2024.100070_bib161
  article-title: Synthesis of imidized cyclobutene derivatives by strain release of [1.1.1]Propellane, org
  publication-title: Letture
– volume: 12
  start-page: 7480
  year: 2021
  ident: 10.1016/j.tchem.2024.100070_bib59
  article-title: Synthesis of 1,3-disubstituted bicyclo[1.1.0]butanes via directed bridgehead functionalization
  publication-title: Chem. Sci.
  doi: 10.1039/D1SC01836A
– volume: 28
  start-page: 857
  year: 2007
  ident: 10.1016/j.tchem.2024.100070_bib19
  article-title: New insights on the bridge carbon–carbon bond in propellanes: a theoretical study based on the analysis of the electron localization function
  publication-title: J. Comput. Chem.
  doi: 10.1002/jcc.20615
– volume: 114
  start-page: 601
  year: 1992
  ident: 10.1016/j.tchem.2024.100070_bib120
  article-title: Toward a molecular-size tinkertoy construction set. Preparation of terminally functionalized [n]staffanes from [1.1.1]propellane
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00028a029
– volume: 145
  start-page: 5363
  year: 2023
  ident: 10.1016/j.tchem.2024.100070_bib140
  article-title: A general and modular approach to BCP alkylamines via multicomponent difunctionalization of [1.1.1]Propellane
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c13298
– volume: 84
  start-page: 15106
  year: 2019
  ident: 10.1016/j.tchem.2024.100070_bib58
  article-title: Difluoro-substituted bicyclo[1.1.1]pentanes for medicinal chemistry: design, synthesis, and characterization
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.9b01947
– volume: 22
  start-page: 6021
  year: 2020
  ident: 10.1016/j.tchem.2024.100070_bib167
  article-title: Copper-catalyzed cross-coupling between alkyl (Pseudo)halides and bicyclopentyl grignard reagents
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.0c02115
SSID ssj0002811299
Score 2.4630945
SecondaryResourceType review_article
Snippet Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties....
SourceID doaj
crossref
elsevier
SourceType Open Website
Enrichment Source
Index Database
Publisher
StartPage 100070
SubjectTerms [1.1.1]Propellanes
Bicyclo[1.1.0]butanes
Strain-release transformation
Title Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes
URI https://dx.doi.org/10.1016/j.tchem.2024.100070
https://doaj.org/article/3de1f1357c704062919d3c9cc7996937
Volume 9
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3PS8MwFA7iyYsoKs5f9ODRzqZN0-aosjEEd9HBQEZoXhPYGNtw28GLf7vvpe3oaV685BDSpP1e6Pte-vo9xu7pS1mWmzLMC1WGApQLlYQihChWLpcON5FX-xzKwUi8jtNxq9QX5YRV8sAVcI9JabnjSZpBhvtNxoqrMgEFkCFTR99Kb1_0ea1gauaPjIhHqEZmyCd0EQr073ksKDUgovLELVfkFftbHqnlZfon7Limh8FTdVun7MAuztjw3RdyCKm-CTqdYNMim7hpgqULzBS-Yb785F3ejSZmi5TProNiUQa-i09WdOg-p8zW9Tkb9XsfL4OwroMQQhKrKCycEiY1UGJjYiVSSHPjMG6yaeEyIxPOS1MkyE1s6bhDNDJDYZnC4FNIK5ILdrhYLuwlCwyAlMJImVshsgJjBdILTAVkLrbgeIfFDSQaapFwesS5brLBZtrjqAlHXeHYYQ-7i1aVRsb-4c-E9W4oCVz7DjS7rs2u_zJ7h8nGUrrmChUHwKmm-1a_-o_Vr9kRTVnlot2ww83X1t4iOdmYO78PsX376f0CDL_fqA
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Strain-release+transformations+of+bicyclo%5B1.1.0%5Dbutanes+and+%5B1.1.1%5Dpropellanes&rft.jtitle=Tetrahedron+chem&rft.au=Qian-Qian+Hu&rft.au=Jie+Chen&rft.au=Yang+Yang&rft.au=Hui+Yang&rft.date=2024-03-01&rft.pub=Elsevier&rft.eissn=2666-951X&rft.volume=9&rft.spage=100070&rft_id=info:doi/10.1016%2Fj.tchem.2024.100070&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_3de1f1357c704062919d3c9cc7996937
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2666-951X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2666-951X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2666-951X&client=summon