The C(sp)-H bond functionalization of thioethers with styrenes with insight into the mechanism

A metal-free inactive C(sp 3 )-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confi...

Full description

Saved in:
Bibliographic Details
Published inOrganic & biomolecular chemistry Vol. 2; no. 29; pp. 5845 - 5851
Main Authors Yan, Zhan, Wang, Nai-Xing, Zhang, Lei-Yang, Wu, Yue-Hua, Li, Jian-Li, She, Meng-Yao, Gao, Xue-Wang, Feng, Ke, Xing, Yalan
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 27.07.2022
Royal Society of Chemistry
Subjects
Chemistry
Chemistry, Organic
Hydrogen bonds
Physical Sciences
Science & Technology
Styrenes
Thioethers
DIFUNCTIONALIZATION
ALKENES
ETHERS
VINYLARENES
ALKYLATION
Online AccessGet full text

Cover

Abstract A metal-free inactive C(sp 3 )-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations. Overcoming the low reactivity of thioethers, a C(sp 3 )-H bond functionalization of thioethers with styrenes using TBHP and DBU involving a radical relay process in metal-free conditions with theoretical questions elaborated is described.
AbstractList A metal-free inactive C(sp 3 )-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations. Overcoming the low reactivity of thioethers, a C(sp 3 )-H bond functionalization of thioethers with styrenes using TBHP and DBU involving a radical relay process in metal-free conditions with theoretical questions elaborated is described.
A metal-free inactive C(sp(3))-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations.
A metal-free inactive C(sp 3 )–H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations.
A metal-free inactive C(sp3)-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations.A metal-free inactive C(sp3)-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations.
A metal-free inactive C(sp3)–H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This transformation has broken through the low activity of thioethers and realized moderate yields. Herein extended experiments were conducted to confirm the radical relay process, reaction energy and intermediate transformations.
Author Zhang, Lei-Yang
Wu, Yue-Hua
Yan, Zhan
Feng, Ke
Wang, Nai-Xing
She, Meng-Yao
Gao, Xue-Wang
Li, Jian-Li
Xing, Yalan
AuthorAffiliation Department of Chemistry
Chinese Academy of Sciences
Technical Institute of Physics and Chemistry
Northwest University
William Paterson University of New Jersey
College of Chemistry and Materials Science
AuthorAffiliation_xml – name: Northwest University
– name: Department of Chemistry
– name: Technical Institute of Physics and Chemistry
– name: Chinese Academy of Sciences
– name: College of Chemistry and Materials Science
– name: William Paterson University of New Jersey
Author_xml – sequence: 1
  givenname: Zhan
  surname: Yan
  fullname: Yan, Zhan
– sequence: 2
  givenname: Nai-Xing
  surname: Wang
  fullname: Wang, Nai-Xing
– sequence: 3
  givenname: Lei-Yang
  surname: Zhang
  fullname: Zhang, Lei-Yang
– sequence: 4
  givenname: Yue-Hua
  surname: Wu
  fullname: Wu, Yue-Hua
– sequence: 5
  givenname: Jian-Li
  surname: Li
  fullname: Li, Jian-Li
– sequence: 6
  givenname: Meng-Yao
  surname: She
  fullname: She, Meng-Yao
– sequence: 7
  givenname: Xue-Wang
  surname: Gao
  fullname: Gao, Xue-Wang
– sequence: 8
  givenname: Ke
  surname: Feng
  fullname: Feng, Ke
– sequence: 9
  givenname: Yalan
  surname: Xing
  fullname: Xing, Yalan
BookMark eNqNkk1v1DAQhi1URD_gwh0pEpdSFPDYSRwfS6AUqVIv5UrkdcbEVdZebEdV-fU4u9siVRzwZcaa5x3Ph4_JgfMOCXkN9ANQLj8OzK8obQUzz8gRVEKUtOby4NFn9JAcx3hLKUjRVC_IIa_bquUSjsiPmxGL7jRu3pWXxcq7oTCz08l6pyb7Wy1O4U2RRusxjRhicWfTWMR0H9Dh_mZdtD_HlG3yGcVijXpUzsb1S_LcqCniq709Id8vvtx0l-XV9ddv3flVqTlUqcSWtrXkDWrZ8IoK3aiaKS2rwQxDbYxAyuohN0WBA-Pa6JaCgnYlYGAggZ-Q013eTfC_ZoypX9uocZqUQz_HnjUSqgaALujbJ-itn0Nud0tVspFCtJl6v6PucOVN1Badxn4T7FqF-57mcbNcKdDlLDnb_6c7m7Zz7fzsUpbSnVQHH2NA0-t9PAVlpx5ovyy5_8yuP22XfJElZ08kDy_9E36zg0PUj9zfH8P_AG-irfI
CitedBy_id crossref_primary_10_1039_D3OB01403G
crossref_primary_10_1002_anie_202314423
crossref_primary_10_1016_j_scp_2025_101955
crossref_primary_10_1021_acs_joc_4c00870
crossref_primary_10_1002_ange_202314423
Cites_doi 10.1002/anie.201913382
10.1002/adsc.201400629
10.1002/ajoc.201600608
10.1021/acs.joc.9b01077
10.1021/acscatal.9b04931
10.1002/anie.201205343
10.1021/acscatal.9b04887
10.1021/acs.chemrev.7b00667
10.1021/cr078412e
10.1002/anie.200503062
10.1039/C7SC01045A
10.1021/acs.orglett.9b01362
10.1038/srep15250
10.1021/acs.joc.1c00031
10.1002/cctc.202000900
10.1002/ejoc.201600632
10.1016/0022-1902(61)80142-5
10.1002/anie.200802215
10.1039/C9SC04199K
10.1021/cr990124y
10.1021/jacs.0c09778
10.1021/acs.orglett.9b03230
10.1021/ja01146a542
10.1002/adsc.201600467
10.1021/cr0684016
10.1039/C9CC00241C
10.1039/D1GC01871J
10.1039/C8CC07828A
10.1002/ejoc.201700341
10.1002/anie.201903726
10.1021/acs.accounts.1c00329
10.1039/c0cs00063a
10.1002/adsc.201801243
10.1021/jacs.9b07607
10.1021/cs400250m
10.1039/C9OB01530B
10.1021/acs.orglett.5b02116
10.1016/S0040-4039(00)77778-1
10.1002/chem.202001414
10.1002/ejoc.201700678
10.1021/acs.joc.9b00029
10.1021/acs.joc.0c01879
10.1021/acscatal.9b04326
10.1002/slct.201904405
10.1021/acs.orglett.0c00287
10.1021/jacs.0c11025
10.1021/acs.orglett.9b00867
10.1021/acs.orglett.6b02692
10.1021/acs.orglett.8b03485
10.1021/jacs.8b06744
10.1038/srep07446
10.1039/c9cc00241c
10.1055/s-0033-1341279
10.1039/c8cc07828a
10.1039/d1gc01871j
10.1055/s-0039-1690987
10.1039/c7sc01045a
10.1039/c9ob01530b
10.1055/s-0040-1706406
10.1039/c9sc04199k
10.1055/s-0039-1690674
ContentType Journal Article
Copyright Copyright Royal Society of Chemistry 2022
Copyright_xml – notice: Copyright Royal Society of Chemistry 2022
DBID AAYXX
CITATION
17B
1KM
1KN
AHQBO
BLEPL
DTL
EGQ
7QO
7T7
7TM
8FD
C1K
FR3
P64
7X8
DOI 10.1039/d2ob00872f
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Current Chemical Reactions
Web of Science - Science Citation Index Expanded - 2022
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Biotechnology Research Abstracts
Industrial and Applied Microbiology Abstracts (Microbiology A)
Nucleic Acids Abstracts
Technology Research Database
Environmental Sciences and Pollution Management
Engineering Research Database
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitle CrossRef
Web of Science
Biotechnology Research Abstracts
Technology Research Database
Nucleic Acids Abstracts
Engineering Research Database
Industrial and Applied Microbiology Abstracts (Microbiology A)
Biotechnology and BioEngineering Abstracts
Environmental Sciences and Pollution Management
MEDLINE - Academic
DatabaseTitleList
Web of Science
CrossRef
MEDLINE - Academic
Biotechnology Research Abstracts
Database_xml – sequence: 1
  dbid: 1KN
  name: Current Chemical Reactions
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1477-0539
EndPage 5851
ExternalDocumentID 000826341000001
10_1039_D2OB00872F
d2ob00872f
GroupedDBID -
0-7
0R
123
1TJ
29N
4.4
70
705
70J
7~J
AAEMU
AAGNR
AAIWI
AANOJ
AAXPP
ABASK
ABDVN
ABFLS
ABGFH
ABRYZ
ACGFS
ACIWK
ACLDK
ACNCT
ACPRK
ADMRA
ADSRN
AENEX
AFOGI
AFRAH
AFVBQ
AGKEF
AGRSR
AGSTE
AGSWI
ALMA_UNASSIGNED_HOLDINGS
ANUXI
ASKNT
AUDPV
BLAPV
BSQNT
C6K
CS3
D0L
DU5
DZ
EBS
ECGLT
EE0
EF-
F5P
GNO
HZ
H~N
IDZ
J3I
JG
KC5
M4U
N9A
O9-
OK1
P2P
R7B
R7C
RCNCU
RNS
RPMJG
RRA
RRC
RSCEA
SKA
SKF
SLH
TN5
TWZ
UCJ
VH6
VQA
WH7
X
XSW
YNT
YZZ
---
-DZ
-~X
0R~
70~
AAJAE
AAMEH
AAWGC
AAXHV
AAYXX
ABEMK
ABJNI
ABPDG
ABXOH
AEFDR
AENGV
AESAV
AETIL
AFLYV
AFRDS
AFRZK
AGEGJ
AHGCF
AKMSF
ALUYA
APEMP
CITATION
GGIMP
H13
HZ~
R56
RAOCF
17B
1KM
1KN
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
7QO
7T7
7TM
8FD
C1K
FR3
P64
7X8
ID FETCH-LOGICAL-c314t-e8085936ec963407c6a52ac94dfdd5ff7e025d539013123cfc801a18b71d21913
ISICitedReferencesCount 8
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000826341000001
ISSN 1477-0520
1477-0539
IngestDate Thu Jul 10 19:28:25 EDT 2025
Mon Jun 30 12:10:44 EDT 2025
Fri May 30 08:09:43 EDT 2025
Fri Aug 29 15:56:22 EDT 2025
Tue Jul 01 01:52:21 EDT 2025
Thu Apr 24 22:58:40 EDT 2025
Thu Jul 28 04:20:51 EDT 2022
IsPeerReviewed true
IsScholarly true
Issue 29
Keywords DIFUNCTIONALIZATION
ALKENES
ETHERS
VINYLARENES
ALKYLATION
Language English
LinkModel OpenURL
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c314t-e8085936ec963407c6a52ac94dfdd5ff7e025d539013123cfc801a18b71d21913
Notes https://doi.org/10.1039/d2ob00872f
Electronic supplementary information (ESI) available. See DOI
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-4853-7961
0000-0003-1176-9969
0000-0001-9520-3254
0000-0002-6408-0615
PMID 35848391
PQID 2694969778
PQPubID 2047497
PageCount 7
ParticipantIDs crossref_primary_10_1039_D2OB00872F
rsc_primary_d2ob00872f
proquest_miscellaneous_2691461101
proquest_journals_2694969778
webofscience_primary_000826341000001
crossref_citationtrail_10_1039_D2OB00872F
webofscience_primary_000826341000001CitationCount
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-07-27
PublicationDateYYYYMMDD 2022-07-27
PublicationDate_xml – month: 07
  year: 2022
  text: 2022-07-27
  day: 27
PublicationDecade 2020
PublicationPlace CAMBRIDGE
PublicationPlace_xml – name: CAMBRIDGE
– name: Cambridge
PublicationTitle Organic & biomolecular chemistry
PublicationTitleAbbrev ORG BIOMOL CHEM
PublicationYear 2022
Publisher Royal Soc Chemistry
Royal Society of Chemistry
Publisher_xml – name: Royal Soc Chemistry
– name: Royal Society of Chemistry
References Bao (D2OB00872F/cit7a/1) 2019
Allred (D2OB00872F/cit17a/1) 1961; 17
Lan (D2OB00872F/cit13/1) 2015; 17
Wang (D2OB00872F/cit10c/1) 2019; 17
Lv (D2OB00872F/cit6d/1) 2019; 21
Wickham (D2OB00872F/cit6h/1) 2021; 54
Fischer (D2OB00872F/cit18a/1) 2001; 101
Zhang (D2OB00872F/cit23b/1) 2014
List (D2OB00872F/cit24b/1) 2007; 107
Joung (D2OB00872F/cit6a/1) 2019; 10
Wei (D2OB00872F/cit7f/1) 2015; 357
Zhang (D2OB00872F/cit11e/1) 2011; 40
Liang (D2OB00872F/cit7b/1) 2019; 10
Lan (D2OB00872F/cit16a/1) 2017
Shi (D2OB00872F/cit2/1) 2019; 84
Zhang (D2OB00872F/cit16b/1) 2019
Zou (D2OB00872F/cit8b/1) 2019; 9
Zhang (D2OB00872F/cit8a/1) 2020; 26
Lu (D2OB00872F/cit19/1) 2017; 6
Xue (D2OB00872F/cit20/1) 2013; 3
Takai (D2OB00872F/cit22/1) 1980; 21
Siu (D2OB00872F/cit6f/1) 2018; 140
Chen (D2OB00872F/cit7h/1) 2020; 5
Xia (D2OB00872F/cit7g/1) 2019; 84
Zhang (D2OB00872F/cit12/1) 2015; 5
Guo (D2OB00872F/cit10a/1) 2016
Chen (D2OB00872F/cit3/1) 2019; 55
Dhungana (D2OB00872F/cit4/1) 2020; 142
Li (D2OB00872F/cit6c/1) 2020; 59
Zhang (D2OB00872F/cit23a/1) 2014; 4
Wang (D2OB00872F/cit6g/1) 2020; 22
Li (D2OB00872F/cit10b/1) 2008; 47
Yang (D2OB00872F/cit7d/1) 2021; 86
Yan (D2OB00872F/cit15/1) 2019; 361
Batra (D2OB00872F/cit11a/1) 2017
Shen (D2OB00872F/cit1b/1) 2020; 85
Wu (D2OB00872F/cit1c/1) 2019; 55
Mahlau (D2OB00872F/cit24c/1) 2013; 52
Lakshman (D2OB00872F/cit11c/1) 2017; 8
Hoffmann (D2OB00872F/cit24a/1) 2005; 44
Li (D2OB00872F/cit6b/1) 2019; 141
Wang (D2OB00872F/cit9/1) 2020; 10
Chiang (D2OB00872F/cit17b/1) 1963; 12
Sun (D2OB00872F/cit7c/1) 2019; 21
Wu (D2OB00872F/cit6i/1) 2020; 12
Leifert (D2OB00872F/cit18b/1) 2020; 59
Kalck (D2OB00872F/cit1a/1) 2018; 118
Zhao (D2OB00872F/cit7e/1) 2019; 21
Tian (D2OB00872F/cit11d/1) 2021; 23
Guo (D2OB00872F/cit11b/1) 2017; 359
Yang (D2OB00872F/cit5/1) 2019; 21
Lan (D2OB00872F/cit14/1) 2016; 18
Xing (D2OB00872F/cit16c/1) 2021
Kornblum (D2OB00872F/cit21/1) 1951; 73
Mukherjee (D2OB00872F/cit24d/1) 2007; 107
Makai (D2OB00872F/cit6e/1) 2020; 142
Zhao, QQ (WOS:000468696100081) 2019; 21
Batra, A (WOS:000405130200001) 2017; 2017
Zhang, JX (WOS:000346300300001) 2014; 4
Lan, XW (WOS:000389396100005) 2016; 18
Sun, X (WOS:000467320000042) 2019; 21
Li, Y (WOS:000499738700018) 2019; 141
Dhungana, RK (WOS:000600204900004) 2020; 142
Guo, SR (WOS:000383624700002) 2016; 2016
Makai, S (WOS:000603395100036) 2020; 142
Wang, YQ (WOS:000516887400033) 2020; 10
Hoffmann, S (WOS:000233515700018) 2005; 44
Lv, XL (WOS:000455285800013) 2019; 21
Xia, ZH (WOS:000471212000077) 2019; 84
Zhang, JX (WOS:000338110700031) 2014; 25
KORNBLUM, N (WOS:A1951UB19800145) 1951; 73
Siu, JC (WOS:000446920100033) 2018; 140
Mukherjee, S (WOS:000251583300003) 2007; 107
Lu, SL (WOS:000397588800014) 2017; 6
Chen, J (WOS:000459022300018) 2019; 55
Tian, T (WOS:000689168300001) 2021; 23
Lakshman, MK (WOS:000408168600002) 2017; 8
Zhang, HH (WOS:000574999300001) 2020; 26
Lan, XW (WOS:000413677500001) 2017; 2017
Zhang, T (WOS:000500764100003) 2019; 51
Zhang, W (WOS:000362874300001) 2015; 5
Zhang, SY (WOS:000288609400009) 2011; 40
Wickham, LM (WOS:000695520400012) 2021; 54
Li, YQ (WOS:000536953100006) 2020; 59
CHIANG, MC (WOS:A19632954C00004) 1963; 12
Mahlau, M (WOS:000312942900005) 2013; 52
Wu, SK (WOS:000457296200001) 2019; 55
Shen, HW (WOS:000589941700031) 2020; 85
Yan, Z (WOS:000461675600014) 2019; 361
Wei, WT (WOS:000347705400008) 2015; 357
Zou, JX (WOS:000502169900074) 2019; 9
Bao, XZ (WOS:000500764100002) 2019; 51
List, B (WOS:000251583300001) 2007; 107
Xue, QC (WOS:000320298800033) 2013; 3
Joung, S (WOS:000501225100012) 2019; 10
Wang, P (WOS:000518875500045) 2020; 22
Guo, SR (WOS:000391812000009) 2017; 359
Yang, XK (WOS:000494553300025) 2019; 21
Li, ZP (WOS:000259477700022) 2008; 47
Wang, NX (WOS:000599193200005) 2021; 32
Lan, XW (WOS:000361867800016) 2015; 17
Leifert, D (WOS:000526984800008) 2020; 59
Chen, RX (WOS:000513245800038) 2020; 5
Wang, X (WOS:000487021800007) 2019; 17
ALLRED, AL (WOS:A1961WN28400004) 1961; 17
Yang, Z (WOS:000631442900022) 2021; 86
Kalck, P (WOS:000430156100013) 2018; 118
Liang, QJ (WOS:000516887400026) 2020; 10
TAKAI, K (WOS:A1980JP72500020) 1980; 21
Wu, YC (WOS:000565613300001) 2020; 12
Shi, Y (WOS:000464250800026) 2019; 84
Fischer, H (WOS:000172874900002) 2001; 101
References_xml – volume: 59
  start-page: 7990
  year: 2020
  ident: D2OB00872F/cit6c/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201913382
– volume: 357
  start-page: 59
  year: 2015
  ident: D2OB00872F/cit7f/1
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201400629
– volume: 12
  start-page: 785
  year: 1963
  ident: D2OB00872F/cit17b/1
  publication-title: Sci. Sin.
– volume: 6
  start-page: 313
  year: 2017
  ident: D2OB00872F/cit19/1
  publication-title: Asian J. Org. Chem.
  doi: 10.1002/ajoc.201600608
– volume: 84
  start-page: 7388
  year: 2019
  ident: D2OB00872F/cit7g/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.9b01077
– volume: 10
  start-page: 2707
  year: 2020
  ident: D2OB00872F/cit9/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b04931
– volume: 52
  start-page: 518
  year: 2013
  ident: D2OB00872F/cit24c/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201205343
– volume: 10
  start-page: 2633
  year: 2019
  ident: D2OB00872F/cit7b/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b04887
– volume: 118
  start-page: 3833
  year: 2018
  ident: D2OB00872F/cit1a/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.7b00667
– volume: 107
  start-page: 5413
  year: 2007
  ident: D2OB00872F/cit24b/1
  publication-title: Chem. Rev.
  doi: 10.1021/cr078412e
– volume: 44
  start-page: 7424
  year: 2005
  ident: D2OB00872F/cit24a/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200503062
– volume: 8
  start-page: 5845
  year: 2017
  ident: D2OB00872F/cit11c/1
  publication-title: Chem. Sci.
  doi: 10.1039/C7SC01045A
– volume: 21
  start-page: 3861
  year: 2019
  ident: D2OB00872F/cit7e/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b01362
– volume: 5
  start-page: 15250
  year: 2015
  ident: D2OB00872F/cit12/1
  publication-title: Sci. Rep.
  doi: 10.1038/srep15250
– volume: 86
  start-page: 4616
  year: 2021
  ident: D2OB00872F/cit7d/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.1c00031
– volume: 12
  start-page: 5312
  year: 2020
  ident: D2OB00872F/cit6i/1
  publication-title: ChemCatChem
  doi: 10.1002/cctc.202000900
– start-page: 4260
  year: 2016
  ident: D2OB00872F/cit10a/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201600632
– volume: 17
  start-page: 215
  year: 1961
  ident: D2OB00872F/cit17a/1
  publication-title: J. Inorg. Nucl. Chem.
  doi: 10.1016/0022-1902(61)80142-5
– volume: 47
  start-page: 7497
  year: 2008
  ident: D2OB00872F/cit10b/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200802215
– volume: 10
  start-page: 10944
  year: 2019
  ident: D2OB00872F/cit6a/1
  publication-title: Chem. Sci.
  doi: 10.1039/C9SC04199K
– volume: 101
  start-page: 3581
  year: 2001
  ident: D2OB00872F/cit18a/1
  publication-title: Chem. Rev.
  doi: 10.1021/cr990124y
– start-page: 23
  year: 2021
  ident: D2OB00872F/cit16c/1
  publication-title: Synlett
– volume: 142
  start-page: 20930
  year: 2020
  ident: D2OB00872F/cit4/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c09778
– volume: 21
  start-page: 8625
  year: 2019
  ident: D2OB00872F/cit5/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b03230
– volume: 73
  start-page: 880
  year: 1951
  ident: D2OB00872F/cit21/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja01146a542
– volume: 359
  start-page: 2
  year: 2017
  ident: D2OB00872F/cit11b/1
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201600467
– volume: 107
  start-page: 5471
  year: 2007
  ident: D2OB00872F/cit24d/1
  publication-title: Chem. Rev.
  doi: 10.1021/cr0684016
– volume: 55
  start-page: 2336
  year: 2019
  ident: D2OB00872F/cit3/1
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC00241C
– volume: 23
  start-page: 6789
  year: 2021
  ident: D2OB00872F/cit11d/1
  publication-title: Green Chem.
  doi: 10.1039/D1GC01871J
– volume: 55
  start-page: 883
  year: 2019
  ident: D2OB00872F/cit1c/1
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC07828A
– start-page: 3739
  year: 2017
  ident: D2OB00872F/cit11a/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201700341
– volume: 59
  start-page: 74
  year: 2020
  ident: D2OB00872F/cit18b/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201903726
– volume: 54
  start-page: 3415
  year: 2021
  ident: D2OB00872F/cit6h/1
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.1c00329
– volume: 40
  start-page: 1937
  year: 2011
  ident: D2OB00872F/cit11e/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c0cs00063a
– volume: 361
  start-page: 1007
  year: 2019
  ident: D2OB00872F/cit15/1
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201801243
– volume: 141
  start-page: 18475
  year: 2019
  ident: D2OB00872F/cit6b/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b07607
– volume: 3
  start-page: 1365
  year: 2013
  ident: D2OB00872F/cit20/1
  publication-title: ACS Catal.
  doi: 10.1021/cs400250m
– volume: 17
  start-page: 8364
  year: 2019
  ident: D2OB00872F/cit10c/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C9OB01530B
– volume: 17
  start-page: 4460
  year: 2015
  ident: D2OB00872F/cit13/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b02116
– volume: 21
  start-page: 1657
  year: 1980
  ident: D2OB00872F/cit22/1
  publication-title: Tetrahedron Lett.
  doi: 10.1016/S0040-4039(00)77778-1
– volume: 26
  start-page: 17289
  year: 2020
  ident: D2OB00872F/cit8a/1
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.202001414
– start-page: 5821
  year: 2017
  ident: D2OB00872F/cit16a/1
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201700678
– volume: 84
  start-page: 4017
  year: 2019
  ident: D2OB00872F/cit2/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.9b00029
– volume: 85
  start-page: 13735
  year: 2020
  ident: D2OB00872F/cit1b/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.0c01879
– volume: 9
  start-page: 11426
  year: 2019
  ident: D2OB00872F/cit8b/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b04326
– volume: 5
  start-page: 2078
  year: 2020
  ident: D2OB00872F/cit7h/1
  publication-title: ChemistrySelect
  doi: 10.1002/slct.201904405
– volume: 22
  start-page: 1924
  year: 2020
  ident: D2OB00872F/cit6g/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.0c00287
– volume: 142
  start-page: 21548
  year: 2020
  ident: D2OB00872F/cit6e/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.0c11025
– volume: 21
  start-page: 3167
  year: 2019
  ident: D2OB00872F/cit7c/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00867
– start-page: 4531
  year: 2019
  ident: D2OB00872F/cit16b/1
  publication-title: Synthesis
– volume: 18
  start-page: 5986
  year: 2016
  ident: D2OB00872F/cit14/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.6b02692
– volume: 21
  start-page: 56
  year: 2019
  ident: D2OB00872F/cit6d/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b03485
– volume: 140
  start-page: 12511
  year: 2018
  ident: D2OB00872F/cit6f/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b06744
– start-page: 4507
  year: 2019
  ident: D2OB00872F/cit7a/1
  publication-title: Synthesis
– start-page: 1621
  year: 2014
  ident: D2OB00872F/cit23b/1
  publication-title: Synlett
– volume: 4
  start-page: 7446
  year: 2014
  ident: D2OB00872F/cit23a/1
  publication-title: Sci. Rep.
  doi: 10.1038/srep07446
– volume: 55
  start-page: 2336
  year: 2019
  ident: WOS:000459022300018
  article-title: Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc00241c
– volume: 2016
  start-page: 4260
  year: 2016
  ident: WOS:000383624700002
  article-title: Gold-Catalyzed, Iodine(III)-Mediated Direct Acyloxylation of the Unactivated C(sp3)-H Bonds of Methyl Sulfides
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201600632
– volume: 21
  start-page: 56
  year: 2019
  ident: WOS:000455285800013
  article-title: Rapid Synthesis of γ-Arylated Carbonyls Enabled by the Merge of Copper- and Photocatalytic Radical Relay Alkylarylation of Alkenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b03485
– volume: 141
  start-page: 18475
  year: 2019
  ident: WOS:000499738700018
  article-title: Directed Copper-Catalyzed Intermolecular Aminative Difunctionalization of Unactivated Alkenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b07607
– volume: 6
  start-page: 313
  year: 2017
  ident: WOS:000397588800014
  article-title: Cobalt-Catalyzed Alkylation-Peroxidation of Alkenes with 1,3-Dicarbonyl Compounds and T-Hydro
  publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ajoc.201600608
– volume: 361
  start-page: 1007
  year: 2019
  ident: WOS:000461675600014
  article-title: A Copper (II) Acetate Mediated Oxidative-Coupling of Styrenes and Ethers Through an Unactivated C(sp3)-H Bond Functionalization
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201801243
– volume: 118
  start-page: 3833
  year: 2018
  ident: WOS:000430156100013
  article-title: Tandem Hydroaminomethylation Reaction to Synthesize Amines from Alkenes
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.7b00667
– volume: 9
  start-page: 11426
  year: 2019
  ident: WOS:000502169900074
  article-title: Phthalimide-Carried Disulfur Transfer To Synthesize Unsymmetrical Disulfanes via Copper Catalysis
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b04326
– volume: 17
  start-page: 4460
  year: 2015
  ident: WOS:000361867800016
  article-title: Copper/Manganese Cocatalyzed Oxidative Coupling of Vinylarenes with Ketones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.5b02116
– volume: 2017
  start-page: 5821
  year: 2017
  ident: WOS:000413677500001
  article-title: Recent Advances in Radical Difunctionalization of Simple Alkenes
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201700678
– volume: 5
  start-page: 2078
  year: 2020
  ident: WOS:000513245800038
  article-title: Co-Catalyzed Oxidative Alkylation between Styrenes and Cyclic Ethers via sp3 C-H Functionalization
  publication-title: CHEMISTRYSELECT
  doi: 10.1002/slct.201904405
– volume: 25
  start-page: 1621
  year: 2014
  ident: WOS:000338110700031
  article-title: Nickel-Catalyzed sp3 C-H Bond Activation from Decarboxylative Cross-Coupling of α,β-Unsaturated Carboxylic Acids with Amides
  publication-title: SYNLETT
  doi: 10.1055/s-0033-1341279
– volume: 21
  start-page: 1657
  year: 1980
  ident: WOS:A1980JP72500020
  article-title: SELECTIVE OXIDATION WITH TERT-BUTYL HYDROPEROXIDE AND ALUMINUM REAGENTS
  publication-title: TETRAHEDRON LETTERS
– volume: 4
  start-page: ARTN 7446
  year: 2014
  ident: WOS:000346300300001
  article-title: Selective Nickel- and Manganese-Catalyzed Decarboxylative Cross Coupling of Some α,β-Unsaturated Carboxylic Acids with Cyclic Ethers
  publication-title: SCIENTIFIC REPORTS
  doi: 10.1038/srep07446
– volume: 101
  start-page: 3581
  year: 2001
  ident: WOS:000172874900002
  article-title: The persistent radical effect: A principle for selective radical reactions and living radical polymerizations
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr990124y
– volume: 5
  start-page: ARTN 15250
  year: 2015
  ident: WOS:000362874300001
  article-title: Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols
  publication-title: SCIENTIFIC REPORTS
  doi: 10.1038/srep15250
– volume: 84
  start-page: 7388
  year: 2019
  ident: WOS:000471212000077
  article-title: Visible-Light-Promoted Oxo-difluoroalkylation of Alkenes with DMSO as the Oxidant
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.9b01077
– volume: 40
  start-page: 1937
  year: 2011
  ident: WOS:000288609400009
  article-title: Direct Sp3 α-C-H activation and functionalization of alcohol and ether
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c0cs00063a
– volume: 55
  start-page: 883
  year: 2019
  ident: WOS:000457296200001
  article-title: Biocatalytic selective functionalisation of alkenes via single-step and one-pot multi-step reactions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc07828a
– volume: 47
  start-page: 7497
  year: 2008
  ident: WOS:000259477700022
  article-title: Iron-catalyzed C-C bond formation by direct functionalization of C-H bonds adjacent to heteroatoms
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200802215
– volume: 10
  start-page: 2633
  year: 2020
  ident: WOS:000516887400026
  article-title: Copper-Catalyzed Intermolecular Difunctionalization of Styrenes with Thiosulfonates and Arylboronic Acids via a Radical Relay Pathway
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b04887
– volume: 59
  start-page: 7990
  year: 2020
  ident: WOS:000536953100006
  article-title: Difunctionalization of Alkenes Involving Metal Migration
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201913382
– volume: 23
  start-page: 6789
  year: 2021
  ident: WOS:000689168300001
  article-title: Cross-dehydrogenative coupling: a sustainable reaction for C-C bond formations
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d1gc01871j
– volume: 51
  start-page: 4507
  year: 2019
  ident: WOS:000500764100002
  article-title: Radical-Mediated Difunctionalization of Styrenes
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0039-1690987
– volume: 86
  start-page: 4616
  year: 2021
  ident: WOS:000631442900022
  article-title: Copper-Catalyzed Asymmetric Borylacylation of Styrene and Indene Derivatives
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.1c00031
– volume: 18
  start-page: 5986
  year: 2016
  ident: WOS:000389396100005
  article-title: Unactivated C(sp3)-H Bond Functionalization of Alkyl Nitriles with Vinylarenes and Mechanistic Studies
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.6b02692
– volume: 107
  start-page: 5471
  year: 2007
  ident: WOS:000251583300003
  article-title: Asymmetric enamine catalysis
  publication-title: CHEMICAL REVIEWS
– volume: 142
  start-page: 21548
  year: 2020
  ident: WOS:000603395100036
  article-title: Direct Synthesis of Unprotected 2-Azidoamines from Alkenes via an Iron-Catalyzed Difunctionalization Reaction
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.0c11025
– volume: 140
  start-page: 12511
  year: 2018
  ident: WOS:000446920100033
  article-title: Electrochemical Azidooxygenation of Alkenes Mediated by a TEMPO-N3 Charge-Transfer Complex
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b06744
– volume: 8
  start-page: 5845
  year: 2017
  ident: WOS:000408168600002
  article-title: Cross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c7sc01045a
– volume: 21
  start-page: 8625
  year: 2019
  ident: WOS:000494553300025
  article-title: Silver-Catalyzed Trifluoromethylalkynylation of Unactivated Alkenes with Hypervalent Iodine Reagents
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b03230
– volume: 54
  start-page: 3415
  year: 2021
  ident: WOS:000695520400012
  article-title: Transition Metal (Ni, Cu, Pd)-Catalyzed Alkene Dicarbofunctionalization Reactions
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/acs.accounts.1c00329
– volume: 73
  start-page: 880
  year: 1951
  ident: WOS:A1951UB19800145
  article-title: THE BASE CATALYZED DECOMPOSITION OF A DIALKYL PEROXIDE
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 107
  start-page: 5413
  year: 2007
  ident: WOS:000251583300001
  article-title: Introduction: Organocatalysis
  publication-title: CHEMICAL REVIEWS
– volume: 17
  start-page: 8364
  year: 2019
  ident: WOS:000487021800007
  article-title: Direct methyl C(sp3)-H azolation of thioanisoles via oxidative radical coupling
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c9ob01530b
– volume: 10
  start-page: 2707
  year: 2020
  ident: WOS:000516887400033
  article-title: Dechalcogenization of Aryl Dichalcogenides to Synthesize Aryl Chalcogenides via Copper Catalysis
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b04931
– volume: 3
  start-page: 1365
  year: 2013
  ident: WOS:000320298800033
  article-title: Metal-Free, n-Bu4NI-Catalyzed Regioselective Difunctionalization of Unactivated Alkenes
  publication-title: ACS CATALYSIS
  doi: 10.1021/cs400250m
– volume: 2017
  start-page: 3739
  year: 2017
  ident: WOS:000405130200001
  article-title: Recent Advances in Functionalization of α-C(sp3)-H Centres in Inactivated Ethers through Cross Dehydrogenative Coupling
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201700341
– volume: 357
  start-page: 59
  year: 2015
  ident: WOS:000347705400008
  article-title: Oxidative Coupling of Alkenes with Aldehydes and Hydroperoxides: One-Pot Synthesis of 2,3-Epoxy Ketones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201400629
– volume: 17
  start-page: 215
  year: 1961
  ident: WOS:A1961WN28400004
  article-title: ELECTRONEGATIVITY VALUES FROM THERMOCHEMICAL DATA
  publication-title: JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY
– volume: 44
  start-page: 7424
  year: 2005
  ident: WOS:000233515700018
  article-title: A powerful bronsted acid catalyst for the organocatalytic asymmetric transfer hydrogenation of imines
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200503062
– volume: 12
  start-page: 785
  year: 1963
  ident: WOS:A19632954C00004
  article-title: A QUANTITATIVE RELATIONSHIP BETWEEN MOLECULAR STRUCTURE AND CHEMICAL REACTIVITY .1. INDUCTIVE EFFECT IN NON-CONJUGATED SYSTEMS
  publication-title: SCIENTIA SINICA
– volume: 85
  start-page: 13735
  year: 2020
  ident: WOS:000589941700031
  article-title: Ruthenium-Catalyzed Electrochemical Synthesis of Indolines through Dehydrogenative [3+2] Annulation with H2 Evolution
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.0c01879
– volume: 21
  start-page: 3167
  year: 2019
  ident: WOS:000467320000042
  article-title: Electrochemical Radical Formyloxylation-Bromination, -Chlorination, and -Trifluoromethylation of Alkenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b00867
– volume: 22
  start-page: 1924
  year: 2020
  ident: WOS:000518875500045
  article-title: Intermolecular Trifluoromethyl-Hydrazination of Alkenes Enabled by Organic Photoredox Catalysis
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.0c00287
– volume: 32
  start-page: 23
  year: 2021
  ident: WOS:000599193200005
  article-title: C(sp 3 )-H Bond Functionalization of Alcohols, Ketones, Nitriles, Ethers and Amides using tert -Butyl Hydroperoxide as a Radical Initiator
  publication-title: SYNLETT
  doi: 10.1055/s-0040-1706406
– volume: 359
  start-page: 2
  year: 2017
  ident: WOS:000391812000009
  article-title: Recent Advances of Oxidative Radical Cross-Coupling Reactions: Direct α-C(sp3)-H Bond Functionalization of Ethers and Alcohols
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201600467
– volume: 21
  start-page: 3861
  year: 2019
  ident: WOS:000468696100081
  article-title: Visible-Light-Driven Neutral Nitrogen Radical Mediated Intermolecular Styrene Difunctionalization
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b01362
– volume: 59
  start-page: 74
  year: 2020
  ident: WOS:000526984800008
  article-title: The Persistent Radical Effect in Organic Synthesis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201903726
– volume: 10
  start-page: 10944
  year: 2019
  ident: WOS:000501225100012
  article-title: Ni-catalyzed 1,2-benzylboration of 1,2-disubstituted unactivated alkenes
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c9sc04199k
– volume: 142
  start-page: 20930
  year: 2020
  ident: WOS:000600204900004
  article-title: Ni-Catalyzed Regioselective 1,2-Dialkylation of Alkenes Enabled by the Formation of Two C(sp3)-C(sp3) Bonds
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.0c09778
– volume: 51
  start-page: 4531
  year: 2019
  ident: WOS:000500764100003
  article-title: Advances in C(sp3)-H Bond Functionalization via Radical Processes
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0039-1690674
– volume: 12
  start-page: 5312
  year: 2020
  ident: WOS:000565613300001
  article-title: Recent Advances in Silver-Mediated Radical Difunctionalization of Alkenes
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.202000900
– volume: 52
  start-page: 518
  year: 2013
  ident: WOS:000312942900005
  article-title: Asymmetric Counteranion-Directed Catalysis: Concept, Definition, and Applications
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201205343
– volume: 84
  start-page: 4017
  year: 2019
  ident: WOS:000464250800026
  article-title: Lipophilic Indole-Catalyzed Intermolecular Bromoesterification of Olefins in Nonpolar Media
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.9b00029
– volume: 26
  start-page: 17289
  year: 2020
  ident: WOS:000574999300001
  article-title: Recent Advances in Iodine-Promoted C-S/N-S Bonds Formation
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.202001414
SSID ssj0019764
Score 2.4176989
Snippet A metal-free inactive C(sp 3 )-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This...
A metal-free inactive C(sp 3 )–H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This...
A metal-free inactive C(sp(3))-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This...
A metal-free inactive C(sp3)–H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This...
A metal-free inactive C(sp3)-H bond functionalization of thioethers with styrenes using TBHP as an initiator and DBU as a base has been developed. This...
Source Web of Science
SourceID proquest
webofscience
crossref
rsc
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 5845
SubjectTerms Chemistry
Chemistry, Organic
Hydrogen bonds
Physical Sciences
Science & Technology
Styrenes
Thioethers
Title The C(sp)-H bond functionalization of thioethers with styrenes with insight into the mechanism
URI http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000826341000001
https://www.proquest.com/docview/2694969778
https://www.proquest.com/docview/2691461101
Volume 2
WOS 000826341000001
WOSCitedRecordID wos000826341000001
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF6FVoJeEK-KQEGL6IEqWsjau45zLKFVQKUcSEVu1nq9liLROGriC_-P_8XMPmy35BC4WLG98Ws-z3wznpkl5FiNgRVIpVgZ5ZIJk5ZMGZUwLpXQpRSRsX26v14m0yvxZS7nvd7vTtZSvcnf619b60r-R6qwDeSKVbL_INnmoLABfoN8YQkShuXOMp4ARVyvMF7KpoMcq1HQVLkIn6-xdHkAi8rW9vpytjVGn0HNubXFco1OOjaPcFT02mBFcGgv6Mmrq9vUFi1Yth9m1h3oMGtco0NcWBWj0W3E3mmVS7Vg82AvuxHrC7Ng8L9mx4_amofasGmtusGJyCayulp_n9WEIZDvlR5Mbl2I07ViNGKYhuNMUXeb628UFLQf4YDo4yNO3QJ7kh3TjZ84t5qFYYxdVYuoyrEFX1R2B4FIV9cWIDEcDvgib01jSAe4YzGbPEbLoBIgAtbXAid8PwJvBdTt_unZ7PNF8zkLOJ9Nbwh3HPrkxuMP7UUdkPvhCm6TpNbzuXez1lsZkmVDs0fkoXdj6KnD5GPSM8sn5EHz-J-SDLBJJ-8AmSdsShGX9C9c0qqkLS4pIpEGXLo1j0uKuIShhja4fEauzs9mkynzk3kwHXOxYSa1rfUSo0Hli-FIJ0pGSo9FURaFLMuRAfZdSAzBxcCmdKmBOyme5iNegFXl8SHZW1ZL85xQWXBdCiXTfCgEeofclGDvVZLmueJx2icn4ell2ne6xwlXfmY24yIeZ5-ibx_tQz_vk7fN2JXr77J11FEQQubf_3WGNeDjBPwnOOGbZjc8Zvzkppamqu0YoCJAsXmfHILwmnO0Yu-T4648mxF3sNUnfJdhE3-_2NFi82K3Q78kB-27e0T2Nje1eQVUe5O_9kD-A5xAzxM
linkProvider Royal Society of Chemistry
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=The+C%28sp3%29-H+bond+functionalization+of+thioethers+with+styrenes+with+insight+into+the+mechanism&rft.jtitle=Organic+%26+biomolecular+chemistry&rft.au=Yan%2C+Zhan&rft.au=Wang%2C+Nai-Xing&rft.au=Zhang%2C+Lei-Yang&rft.au=Wu%2C+Yue-Hua&rft.date=2022-07-27&rft.pub=Royal+Soc+Chemistry&rft.issn=1477-0520&rft.eissn=1477-0539&rft.volume=20&rft.issue=29&rft.spage=5845&rft.epage=5851&rft_id=info:doi/10.1039%2Fd2ob00872f&rft_id=info%3Apmid%2F35848391&rft.externalDBID=n%2Fa&rft.externalDocID=000826341000001
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1477-0520&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1477-0520&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1477-0520&client=summon