Recent advances in cascade radical cyclization of radical acceptors for the synthesis of carbo- and heterocycles

Cascade radical cyclization is an attractive synthetic method due to its high atom- and step-economy to construct carbo- and heterocycles, which have wide applications in chemical and life science industries. Radical acceptors with unsaturated bonds play a key role in realizing highly rapid, concise...

Full description

Saved in:
Bibliographic Details
Published inOrganic chemistry frontiers an international journal of organic chemistry Vol. 8; no. 6; pp. 1345 - 1363
Main Authors Liao, Jianhua, Yang, Xiao, Ouyang, Lu, Lai, Yinlong, Huang, Jiuzhong, Luo, Renshi
Format Journal Article
LanguageEnglish
Published London Royal Society of Chemistry 23.03.2021
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Cascade radical cyclization is an attractive synthetic method due to its high atom- and step-economy to construct carbo- and heterocycles, which have wide applications in chemical and life science industries. Radical acceptors with unsaturated bonds play a key role in realizing highly rapid, concise, and efficient cascade radical cyclization. This Review is devoted to highlighting the latest achievements in the development of cascade radical cyclization methodologies for the synthesis of carbo- and heterocycles in this rapidly growing research field. Based on the hybridization of starting materials, this Review includes C(sp)–C(sp) bond, C(sp)–C(sp2) bond, C(sp2)–C(sp2) bond, C(sp2)–C(sp3), and carbon–heteroatom bond coupling cyclization. Representative examples mainly published in last three years will be discussed for each highlighted reaction design and mechanism, providing readers with common tools for future research in cascade radical cyclization.
AbstractList Cascade radical cyclization is an attractive synthetic method due to its high atom- and step-economy to construct carbo- and heterocycles, which have wide applications in chemical and life science industries. Radical acceptors with unsaturated bonds play a key role in realizing highly rapid, concise, and efficient cascade radical cyclization. This Review is devoted to highlighting the latest achievements in the development of cascade radical cyclization methodologies for the synthesis of carbo- and heterocycles in this rapidly growing research field. Based on the hybridization of starting materials, this Review includes C(sp)–C(sp) bond, C(sp)–C(sp2) bond, C(sp2)–C(sp2) bond, C(sp2)–C(sp3), and carbon–heteroatom bond coupling cyclization. Representative examples mainly published in last three years will be discussed for each highlighted reaction design and mechanism, providing readers with common tools for future research in cascade radical cyclization.
Author Ouyang, Lu
Liao, Jianhua
Huang, Jiuzhong
Luo, Renshi
Lai, Yinlong
Yang, Xiao
Author_xml – sequence: 1
  givenname: Jianhua
  surname: Liao
  fullname: Liao, Jianhua
– sequence: 2
  givenname: Xiao
  surname: Yang
  fullname: Yang, Xiao
– sequence: 3
  givenname: Lu
  surname: Ouyang
  fullname: Ouyang, Lu
– sequence: 4
  givenname: Yinlong
  surname: Lai
  fullname: Lai, Yinlong
– sequence: 5
  givenname: Jiuzhong
  surname: Huang
  fullname: Huang, Jiuzhong
– sequence: 6
  givenname: Renshi
  surname: Luo
  fullname: Luo, Renshi
BookMark eNpNjcFKAzEURYNUsNZu_IKA69FkkkwnSylqhYIgui4vLy90pCRtkgr1621RxNW5XC7nXrJRTJEYu5biVgpl77zYJSG1Ue6MjVth2kZLKUb_8gWbljI4YXozM9KKMdu-ElKsHPwnRKTCh8gRCoInnsEPCBuOB9wMX1CHFHkKfzUg0ramXHhImdc18XKIR5ShnGYI2aWGQ_R8TZVyOmmoXLHzAJtC019O2Pvjw9t80Sxfnp7n98sGWylrQ8Fpq1TvyesQtG6d8-iD7pwSnoJRXvVonYJeoemEt9ChJGtcCL31bVATdvPj3ea021Opq4-0z_F4uWqNUMbOpOnVNwjDYII
CitedBy_id crossref_primary_10_1002_ejoc_202100868
crossref_primary_10_1039_D3OB01659E
crossref_primary_10_1055_s_0040_1719872
crossref_primary_10_1021_acs_orglett_2c03884
crossref_primary_10_1002_cphc_202300426
crossref_primary_10_1021_acs_joc_4c00766
crossref_primary_10_1002_chem_202301147
crossref_primary_10_1002_adsc_202401516
crossref_primary_10_1039_D1RA05773A
crossref_primary_10_1039_D4GC06598K
crossref_primary_10_3390_molecules29020458
crossref_primary_10_1002_adsc_202400026
crossref_primary_10_1039_D2OB01277D
crossref_primary_10_1002_chem_202301390
crossref_primary_10_1039_D2GC03017A
crossref_primary_10_1021_acs_orglett_4c03386
crossref_primary_10_1016_j_tet_2022_133216
crossref_primary_10_1021_acs_orglett_1c03700
crossref_primary_10_1039_D2QO00518B
crossref_primary_10_1002_ajoc_202300252
crossref_primary_10_1002_anie_202314208
crossref_primary_10_1016_j_gresc_2024_04_008
crossref_primary_10_1002_adsc_202400419
crossref_primary_10_1002_ajoc_202400022
crossref_primary_10_1021_acs_orglett_1c04082
crossref_primary_10_1021_acs_joc_3c01884
crossref_primary_10_1021_acs_joc_4c01746
crossref_primary_10_1002_ange_202404679
crossref_primary_10_1039_D2QO01723G
crossref_primary_10_1039_D4OB00513A
crossref_primary_10_1039_D3OB00789H
crossref_primary_10_1016_j_gresc_2023_10_001
crossref_primary_10_1039_D2OB01207C
crossref_primary_10_1039_D3QO01482G
crossref_primary_10_1002_ange_202402109
crossref_primary_10_1016_j_tet_2023_133409
crossref_primary_10_1039_D4OB01582G
crossref_primary_10_1002_asia_202401502
crossref_primary_10_1002_ejoc_202500158
crossref_primary_10_1002_ajoc_202300101
crossref_primary_10_1039_D2QO00319H
crossref_primary_10_1039_D2OB01833K
crossref_primary_10_1039_D3QO01466E
crossref_primary_10_1002_adsc_202401539
crossref_primary_10_1002_adsc_202300680
crossref_primary_10_21597_jist_1295186
crossref_primary_10_1021_acs_orglett_3c04246
crossref_primary_10_1002_cjoc_202400310
crossref_primary_10_1002_adsc_202401015
crossref_primary_10_1002_anie_202405863
crossref_primary_10_1021_acs_joc_4c00946
crossref_primary_10_6023_A24030090
crossref_primary_10_1021_acs_joc_1c01832
crossref_primary_10_1038_s41570_023_00479_w
crossref_primary_10_1039_D1OB01431E
crossref_primary_10_1021_acsomega_4c01177
crossref_primary_10_1016_j_tetlet_2023_154664
crossref_primary_10_1039_D4OB01583E
crossref_primary_10_1021_acs_orglett_1c04133
crossref_primary_10_1039_D3QO00290J
crossref_primary_10_1002_adsc_202401007
crossref_primary_10_1039_D4OB01733A
crossref_primary_10_1002_asia_202201149
crossref_primary_10_1021_acs_joc_5c00140
crossref_primary_10_1021_acsomega_3c02270
crossref_primary_10_1002_ejoc_202400450
crossref_primary_10_1002_anie_202214812
crossref_primary_10_1002_ange_202405863
crossref_primary_10_1039_D3CC02248J
crossref_primary_10_1002_chem_202103334
crossref_primary_10_1039_D2OB00612J
crossref_primary_10_1002_adsc_202201054
crossref_primary_10_1002_anie_202402109
crossref_primary_10_1039_D4CC05086J
crossref_primary_10_1055_s_0042_1751451
crossref_primary_10_1021_acs_joc_4c01492
crossref_primary_10_6023_cjoc202209029
crossref_primary_10_1021_acs_joc_4c00444
crossref_primary_10_1021_acs_joc_4c02469
crossref_primary_10_1016_j_tetlet_2023_154757
crossref_primary_10_6023_cjoc202209025
crossref_primary_10_1039_D2QO00919F
crossref_primary_10_1021_acs_orglett_4c03744
crossref_primary_10_1002_anie_202404679
crossref_primary_10_1002_adsc_202400189
crossref_primary_10_1039_D3OB00974B
crossref_primary_10_1021_acs_orglett_3c03930
crossref_primary_10_1039_D3OB00744H
crossref_primary_10_1002_ange_202214812
crossref_primary_10_1038_s41467_022_33730_x
crossref_primary_10_1055_a_1959_1930
crossref_primary_10_1021_acs_joc_4c02910
crossref_primary_10_1039_D3GC01841E
crossref_primary_10_1002_asia_202401079
crossref_primary_10_1021_acsomega_2c04205
crossref_primary_10_1039_D3SC05229J
crossref_primary_10_1021_acs_joc_1c02593
crossref_primary_10_1021_acs_joc_3c01964
crossref_primary_10_1002_adsc_202200183
crossref_primary_10_1021_acs_orglett_4c01176
crossref_primary_10_1021_acs_orglett_4c03475
crossref_primary_10_1002_cctc_202200260
crossref_primary_10_1002_ejoc_202301148
crossref_primary_10_1002_slct_202301989
crossref_primary_10_1016_j_tet_2022_132753
crossref_primary_10_1021_acs_orglett_2c03629
crossref_primary_10_1002_ange_202314208
crossref_primary_10_1021_acssuschemeng_3c05380
crossref_primary_10_1039_D4OB01368A
crossref_primary_10_1039_D4GC05637J
crossref_primary_10_1038_s42004_024_01368_z
crossref_primary_10_1016_j_tetlet_2023_154617
crossref_primary_10_1002_adsc_202301295
crossref_primary_10_1039_D3OB00601H
crossref_primary_10_1039_D2QO00188H
crossref_primary_10_1002_adsc_202400762
crossref_primary_10_1021_acs_joc_3c01213
crossref_primary_10_1039_D4OB00732H
crossref_primary_10_1021_acs_orglett_4c02910
crossref_primary_10_1039_D1CC02322E
crossref_primary_10_1039_D2QO00774F
crossref_primary_10_1039_D4CC01970A
crossref_primary_10_1039_D3OB02044D
crossref_primary_10_1039_D3QO00865G
crossref_primary_10_1021_acs_orglett_3c02423
crossref_primary_10_1039_D4GC03260H
crossref_primary_10_1002_adsc_202200049
crossref_primary_10_1039_D2QO01154A
crossref_primary_10_1039_D4OB01632G
crossref_primary_10_1055_a_1890_7743
crossref_primary_10_1039_D4CC03302G
crossref_primary_10_1039_D4QO01461H
crossref_primary_10_1055_a_2039_1728
crossref_primary_10_1002_slct_202300146
crossref_primary_10_1002_ajoc_202200183
crossref_primary_10_3390_molecules29091971
crossref_primary_10_1039_D2QO00175F
crossref_primary_10_1002_ajoc_202400242
crossref_primary_10_1021_acs_orglett_4c00981
crossref_primary_10_1039_D4SC06684G
crossref_primary_10_1016_j_jcat_2022_12_033
crossref_primary_10_1021_acs_joc_1c02335
ContentType Journal Article
Copyright Copyright Royal Society of Chemistry 2021
Copyright_xml – notice: Copyright Royal Society of Chemistry 2021
DBID 7QO
7SR
8BQ
8FD
FR3
JG9
P64
DOI 10.1039/d0qo01453b
DatabaseName Biotechnology Research Abstracts
Engineered Materials Abstracts
METADEX
Technology Research Database
Engineering Research Database
Materials Research Database
Biotechnology and BioEngineering Abstracts
DatabaseTitle Materials Research Database
Engineered Materials Abstracts
Biotechnology Research Abstracts
Technology Research Database
Engineering Research Database
METADEX
Biotechnology and BioEngineering Abstracts
DatabaseTitleList Materials Research Database
DeliveryMethod fulltext_linktorsrc
EISSN 2052-4110
EndPage 1363
GroupedDBID 0R~
7QO
7SR
8BQ
8FD
AAEMU
AAIWI
AAJAE
AANOJ
AARTK
AAXHV
ABASK
ABDVN
ABJNI
ABPDG
ABRYZ
ACGFS
ACIWK
ACLDK
ACPRK
ADMRA
ADSRN
AEFDR
AENGV
AETIL
AFOGI
AFRAH
AFRZK
AGEGJ
AGRSR
AKBGW
AKMSF
ALMA_UNASSIGNED_HOLDINGS
ANUXI
ASKNT
BLAPV
C6K
EBS
ECGLT
FR3
GGIMP
H13
HZ~
JG9
O-G
O9-
P64
RAOCF
RCNCU
RRC
RSCEA
RVUXY
ID FETCH-LOGICAL-c211t-efb49338ded4ff442bbdcdf46b30def53d38c9b3a83c560d9a6c1e95bff89d2f3
ISSN 2052-4110
IngestDate Mon Jun 30 09:36:25 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 6
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c211t-efb49338ded4ff442bbdcdf46b30def53d38c9b3a83c560d9a6c1e95bff89d2f3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
PQID 2503597158
PQPubID 2048884
PageCount 19
ParticipantIDs proquest_journals_2503597158
PublicationCentury 2000
PublicationDate 20210323
PublicationDateYYYYMMDD 2021-03-23
PublicationDate_xml – month: 3
  year: 2021
  text: 20210323
  day: 23
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
PublicationTitle Organic chemistry frontiers an international journal of organic chemistry
PublicationYear 2021
Publisher Royal Society of Chemistry
Publisher_xml – name: Royal Society of Chemistry
SSID ssib058575190
ssj0001256057
Score 2.5673585
Snippet Cascade radical cyclization is an attractive synthetic method due to its high atom- and step-economy to construct carbo- and heterocycles, which have wide...
SourceID proquest
SourceType Aggregation Database
StartPage 1345
SubjectTerms Carbon cycle
Hybridization
Organic chemistry
Title Recent advances in cascade radical cyclization of radical acceptors for the synthesis of carbo- and heterocycles
URI https://www.proquest.com/docview/2503597158
Volume 8
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF6F9MIFURXEo1R76K0yeL1rxz5WKFVBoVwcKT1F-1QjVTYk9iH8O_4Zs96xY9EKARcnGscba-fT7uzMNzOEnBdxomTOWJQV1kRC2CySuZtFhikVZzabZdYnOH-5ya6X4vMqXU0mP0espbZR7_WPR_NK_kerIAO9-izZf9DsMCgI4DvoF66gYbj-lY7B5uso4iGO3zFbtdx5xvvFVoYAjN7re0y19HZhL5ba01l8o52eZrjbV_CB5Um03Ko66gILd54vU_thkG2IlmxI4tQXuu8Y5zNVqsZ31obnujIUB0_jqD5F_ftzAyVoI0MUCAB71w67xS06tFdwe_AIt3uULtrh8dBX-3ZT3de4G6MzI-nYXCHfGFlQ3mXS81U7Psr4XbplMYnTJBIMybD2ERmu6_kIvuM1mvFQwBL3e8bDCvtgL4m5L8Vq4u-1D71yddgxe5bAzdf11XKxWJfzVfmEHCVwUkmm5OhyXn5a9Ita6lugMgxFBscfGJldBdrhrfuyubz4cPi7B8ZBZ_GUz8kzPKrQy4C7YzKx1Qn5FjBHe8zRTUURcxTBRUeYo7UbxAPmKGCOAtjogDn_s4A5CpijY8y9IMurefnxOsKuHZFOGGsi65QoOM-NNcI5IRKljDZOZIrHxrqUG57rQnGZcw0zYQqZaWaLVDmXFyZx_CWZVnVlXxEqbQr2qUmFkFLAPIKtzGY2dYoXMII0r8lpP0VrBPJuDTY9h1MyS_M3f779ljw9QPCUTJtta9-BhdmoM9ThL2MAhrA
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=Recent+advances+in+cascade+radical+cyclization+of+radical+acceptors+for+the+synthesis+of+carbo-+and+heterocycles&rft.jtitle=Organic+chemistry+frontiers+an+international+journal+of+organic+chemistry&rft.au=Liao%2C+Jianhua&rft.au=Yang%2C+Xiao&rft.au=Ouyang%2C+Lu&rft.au=Lai%2C+Yinlong&rft.date=2021-03-23&rft.pub=Royal+Society+of+Chemistry&rft.issn=2052-4110&rft.eissn=2052-4110&rft.volume=8&rft.issue=6&rft.spage=1345&rft.epage=1363&rft_id=info:doi/10.1039%2Fd0qo01453b&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2052-4110&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2052-4110&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2052-4110&client=summon