Selective photoredox decarboxylation of α-ketoacids to allylic ketones and 1,4-dicarbonyl compounds dependent on cobaloxime catalysis

A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The gener...

Full description

Saved in:
Bibliographic Details
Published inChemical communications (Cambridge, England) Vol. 56; no. 83; pp. 1253 - 12533
Main Authors Zhang, Hong, Xiao, Qian, Qi, Xu-Kuan, Gao, Xue-Wang, Tong, Qing-Xiao, Zhong, Jian-Ji
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 20.10.2020
Royal Society of Chemistry
Subjects
Alkenes
Carbonyl compounds
Catalysis
Catalysts
catalytic activity
Chemistry
Chemistry, Multidisciplinary
Decarboxylation
Dehydrogenation
Ketones
Physical Sciences
redox reactions
Science & Technology
Substrates
FUNCTIONALIZATION
HYDROGEN
ACIDS
CHEMISTRY
RADICAL REACTIONS
HIGHLY EFFICIENT
WATER
Online AccessGet full text

Cover

Abstract A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins. The selective synthesis of allylic ketones and 1,4-dicarbonyl compounds by photoredox/cobaloxime co-catalysis and photoredox catalysis, respectively, is described herein.
AbstractList A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins. The selective synthesis of allylic ketones and 1,4-dicarbonyl compounds by photoredox/cobaloxime co-catalysis and photoredox catalysis, respectively, is described herein.
A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins.
A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins.A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins.
A photoredox/cobaloxime co-catalyzed coupling reaction of a-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime catalyst, 1,4-dicarbonyl compounds are generated. The cobaloxime catalyst enables dehydrogenation to generate the formation of new olefins. The generality, good substrate scope and mild conditions are good features in the photoredox/cobaloxime catalysis protocol, and this method will provide new opportunities for the functionalization of more olefins.
Author Tong, Qing-Xiao
Zhang, Hong
Gao, Xue-Wang
Xiao, Qian
Qi, Xu-Kuan
Zhong, Jian-Ji
AuthorAffiliation Key Laboratory of Photochemical Conversion and Optoelectronic Materials
Shantou University, and Chemistry and Chemical Engineering Laboratory of Guangdong Province
Chinese Academy of Sciences
Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province
Technical Institute of Physics and Chemistry
AuthorAffiliation_xml – name: Key Laboratory of Photochemical Conversion and Optoelectronic Materials
– name: Shantou University, and Chemistry and Chemical Engineering Laboratory of Guangdong Province
– name: Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province
– name: Technical Institute of Physics and Chemistry
– name: Chinese Academy of Sciences
Author_xml – sequence: 1
  givenname: Hong
  surname: Zhang
  fullname: Zhang, Hong
– sequence: 2
  givenname: Qian
  surname: Xiao
  fullname: Xiao, Qian
– sequence: 3
  givenname: Xu-Kuan
  surname: Qi
  fullname: Qi, Xu-Kuan
– sequence: 4
  givenname: Xue-Wang
  surname: Gao
  fullname: Gao, Xue-Wang
– sequence: 5
  givenname: Qing-Xiao
  surname: Tong
  fullname: Tong, Qing-Xiao
– sequence: 6
  givenname: Jian-Ji
  surname: Zhong
  fullname: Zhong, Jian-Ji
BookMark eNqNkkuO1DAQhiM0iHnAhj2SERsEBOzYTuIlCo9BGokFILGLnHJF48FtZ2I3dC7AfbgIZ8LdPYA0QoA3Lvn__rJdVcfFgQ8ei-Iuo08Z5eqZoQBUypae3yiOGK9FKUX78WAbS1U2XMjD4jjGC5oXk-2t4pBXqq4FbY-Kr-_QIST7Gcl0HlKY0YQNMQh6HsJmcTrZ4EkYyfdv5SdMQYM1kaRAtHOLs0C2hx4j0d4Q9kSUxu6sfnEEwmoKa595gxN6gz6RnAzCoF3Y2BUS0Em7Jdp4u7g5ahfxztV-Unx49fJ9d1qevX39pnt-VgJveCqVARCVoHQ0fIBGUcqZHBkCF0i5EbVEbVo5tnqAtq5Vo5pB141WzWjqtmL8pHi4zzvN4XKNMfUrGwGd0x7DOvaVrETFBJXNv1EhpGokq2RGH1xDL8J69vkjmZIVVSoXO1OP99QXHMIYwaIH7KfZrvS89Lk3suU1bViOxPal7f_TnU27RnW53Clb6d4Kc4hxxrGHKz3N2rqe0X47N_0L2nW7uTnNlkfXLD9v-iN8bw_PEX5xv4cw6_f_pveTGfkPjQvYJw
CitedBy_id crossref_primary_10_1021_acs_joc_4c02163
crossref_primary_10_1021_acs_orglett_0c03663
crossref_primary_10_1055_a_2535_0823
crossref_primary_10_1039_D1CS00198A
crossref_primary_10_1039_D4CC06594H
crossref_primary_10_6023_cjoc202209025
crossref_primary_10_1002_chem_202301147
crossref_primary_10_1021_acscatal_1c05318
crossref_primary_10_1039_D2QO00957A
crossref_primary_10_3390_molecules27030619
crossref_primary_10_1002_ejoc_202401156
crossref_primary_10_1039_D2SC02277J
crossref_primary_10_1039_D4CC01914H
crossref_primary_10_1021_acs_joc_3c01078
crossref_primary_10_1002_ejoc_202300166
crossref_primary_10_1021_acs_joc_1c01610
crossref_primary_10_1002_anie_202112370
crossref_primary_10_1002_ajoc_202100011
crossref_primary_10_1021_acs_orglett_1c03700
crossref_primary_10_1021_acs_chemrev_3c00755
crossref_primary_10_1021_acs_joc_4c02011
crossref_primary_10_6023_cjoc202304010
crossref_primary_10_1021_acs_orglett_1c00999
crossref_primary_10_1021_acs_joc_4c00799
crossref_primary_10_1016_j_ijhydene_2024_09_284
crossref_primary_10_1039_D2GC01381A
crossref_primary_10_6023_cjoc202302018
crossref_primary_10_1002_cjoc_202300118
crossref_primary_10_1002_ajoc_202300408
crossref_primary_10_1039_D2CC06945H
crossref_primary_10_1039_D1OB01307F
crossref_primary_10_1021_acs_joc_1c00998
crossref_primary_10_1002_ange_202112370
crossref_primary_10_1016_j_tetlet_2024_155153
Cites_doi 10.1002/anie.201200223
10.1002/adsc.201701567
10.1039/C9CC04977K
10.1021/acscatal.5b00093
10.1021/jacs.5b05665
10.1039/C6CC04109D
10.1021/acscatal.7b03719
10.1093/nsr/nwx039
10.1039/C9CC03210J
10.1021/acs.accounts.6b00288
10.1021/acs.chemrev.6b00057
10.1039/cs9881700361
10.1021/acs.orglett.6b00802
10.1002/anie.201904707
10.1002/adsc.202000116
10.1021/cr00006a006
10.1021/jacs.8b11218
10.1002/anie.201007987
10.1021/jacs.6b05498
10.1021/ja010674p
10.1021/acs.chemrev.9b00045
10.1021/acs.chemrev.8b00782
10.1038/nchem.687
10.1002/anie.201505731
10.1021/ar900253e
10.1021/ar50004a001
10.1002/anie.201104681
10.1038/nature11687
10.1021/jo00028a075
10.1021/ol500534w
10.1021/jacs.9b06920
10.1007/s11426-018-9399-2
10.1002/cssc.201402606
10.1021/jacs.8b07327
10.1039/C7CC03823B
10.1021/acs.orglett.8b01085
10.1021/acs.orglett.8b03840
10.1002/anie.201308614
10.1021/acs.accounts.6b00270
10.1038/s41557-018-0142-4
10.1002/anie.201612486
10.1021/acs.accounts.8b00267
10.1021/cr300503r
10.1039/C8SC05600E
10.1021/acs.orglett.6b01353
10.1021/jo00062a031
10.1002/anie.201506432
10.1039/C9CC08512B
10.1002/anie.201503479
10.1002/anie.200904056
10.1021/ja903044n
10.1002/chem.201204572
10.1021/acs.orglett.7b01391
10.1021/ja408486v
10.1021/ol7019839
10.6023/A16090491
10.1016/j.scib.2019.02.002
10.1039/C9CS00523D
10.1002/anie.201105235
10.1039/c7cc03823b
10.1038/NCHEM.687
10.1039/c9cc08512b
10.1007/s11426-017-9165-4
10.1039/c6cc04109d
10.1039/c8sc05600e
10.1039/c9cc03210j
10.1039/c9cc04977k
10.1039/c9cs00523d
ContentType Journal Article
Copyright Copyright Royal Society of Chemistry 2020
Copyright_xml – notice: Copyright Royal Society of Chemistry 2020
DBID AAYXX
CITATION
17B
1KM
1KN
AOWDO
BLEPL
DTL
EGQ
7SR
7U5
8BQ
8FD
JG9
L7M
7X8
7S9
L.6
DOI 10.1039/d0cc05580h
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Current Chemical Reactions
Web of Science - Science Citation Index Expanded - 2020
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Engineered Materials Abstracts
Solid State and Superconductivity Abstracts
METADEX
Technology Research Database
Materials Research Database
Advanced Technologies Database with Aerospace
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
DatabaseTitle CrossRef
Web of Science
Materials Research Database
Engineered Materials Abstracts
Solid State and Superconductivity Abstracts
Technology Research Database
Advanced Technologies Database with Aerospace
METADEX
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
DatabaseTitleList
Materials Research Database
MEDLINE - Academic
CrossRef
AGRICOLA
Web of Science
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 1364-548X
EndPage 12533
ExternalDocumentID 000583607100041
10_1039_D0CC05580H
d0cc05580h
GrantInformation_xml – fundername: Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme 2019
  grantid: GDUPS2019
– fundername: STU Scientific Research Foundation for Talents
  grantid: NTF18003
– fundername: National Natural Science Foundation of China; National Natural Science Foundation of China (NSFC)
  grantid: 21801163; 21702213
GroupedDBID -
0-7
0R
1TJ
29B
4.4
53G
5GY
70
705
70J
7~J
AAEMU
AAGNR
AAIWI
AANOJ
ABDVN
ABFLS
ABGFH
ABPTK
ABRYZ
ACGFS
ACIWK
ACLDK
ACNCT
ADMRA
ADSRN
AENEX
AFVBQ
AGKEF
AGSTE
AGSWI
ALMA_UNASSIGNED_HOLDINGS
ASKNT
AUDPV
AZFZN
BLAPV
BSQNT
C6K
CKLOX
CS3
DU5
DZ
EBS
ECGLT
EE0
EF-
F5P
GNO
H13
HZ
H~N
IDZ
IH2
J3I
JG
M4U
N9A
O9-
P2P
R7B
R7C
R7D
RCNCU
RIG
RPMJG
RRA
RRC
RSCEA
SJN
SKA
SKF
SKH
SLH
TN5
TWZ
UPT
VH6
VQA
WH7
X
X7L
---
-DZ
-~X
0R~
2WC
6J9
70~
AAHBH
AAJAE
AAMEH
AAWGC
AAXHV
AAXPP
AAYXX
ABASK
ABEMK
ABJNI
ABPDG
ABXOH
ACBEA
ACGFO
AEFDR
AENGV
AESAV
AETIL
AFLYV
AFOGI
AFRDS
AFRZK
AGEGJ
AGRSR
AHGCF
AKMSF
ALUYA
ANUXI
APEMP
CITATION
GGIMP
HZ~
R56
RAOCF
17B
1KM
1KN
BLEPL
DTL
GROUPED_WOS_WEB_OF_SCIENCE
7SR
7U5
8BQ
8FD
JG9
L7M
7X8
7S9
L.6
ID FETCH-LOGICAL-c373t-9dcc42400fd3bc7900315f1ec34e03d465ead85f8abc8669797ba67a97fd68213
ISICitedReferencesCount 36
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000583607100041
ISSN 1359-7345
1364-548X
IngestDate Fri Jul 11 07:35:34 EDT 2025
Fri Jul 11 10:30:39 EDT 2025
Sun Jun 29 12:31:16 EDT 2025
Fri Aug 29 16:07:14 EDT 2025
Fri May 30 00:37:39 EDT 2025
Thu Apr 24 23:05:36 EDT 2025
Tue Jul 01 04:09:17 EDT 2025
Sat Jan 08 03:54:52 EST 2022
Wed Nov 11 00:36:16 EST 2020
IsPeerReviewed true
IsScholarly true
Issue 83
Keywords FUNCTIONALIZATION
HYDROGEN
ACIDS
CHEMISTRY
RADICAL REACTIONS
HIGHLY EFFICIENT
WATER
Language English
LinkModel OpenURL
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c373t-9dcc42400fd3bc7900315f1ec34e03d465ead85f8abc8669797ba67a97fd68213
Notes Electronic supplementary information (ESI) available. See DOI
10.1039/d0cc05580h
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-5248-5538
0000-0003-0803-0071
PMID 32966408
PQID 2452099640
PQPubID 2047502
ParticipantIDs webofscience_primary_000583607100041CitationCount
rsc_primary_d0cc05580h
webofscience_primary_000583607100041
crossref_citationtrail_10_1039_D0CC05580H
crossref_primary_10_1039_D0CC05580H
proquest_miscellaneous_2524214057
proquest_miscellaneous_2445975125
proquest_journals_2452099640
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20201020
PublicationDateYYYYMMDD 2020-10-20
PublicationDate_xml – month: 10
  year: 2020
  text: 20201020
  day: 20
PublicationDecade 2020
PublicationPlace CAMBRIDGE
PublicationPlace_xml – name: CAMBRIDGE
– name: Cambridge
PublicationTitle Chemical communications (Cambridge, England)
PublicationTitleAbbrev CHEM COMMUN
PublicationYear 2020
Publisher Royal Soc Chemistry
Royal Society of Chemistry
Publisher_xml – name: Royal Soc Chemistry
– name: Royal Society of Chemistry
References Luo (D0CC05580H-(cit11i)/*[position()=1]) 2019; 55
Capaldo (D0CC05580H-(cit11f)/*[position()=1]) 2018; 8
Zhang (D0CC05580H-(cit4f)/*[position()=1]) 2015; 137
Pattenden (D0CC05580H-(cit6b)/*[position()=1]) 1988; 17
Liu (D0CC05580H-(cit12b)/*[position()=1]) 2014; 53
Cao (D0CC05580H-(cit5f)/*[position()=1]) 2018; 140
Cui (D0CC05580H-(cit10c)/*[position()=1]) 2016; 18
Genovino (D0CC05580H-(cit11g)/*[position()=1]) 2018; 20
Hu (D0CC05580H-(cit7d)/*[position()=1]) 2019; 55
Xuan (D0CC05580H-(cit2j)/*[position()=1]) 2020; 49
Romero (D0CC05580H-(cit2e)/*[position()=1]) 2016; 116
Wang (D0CC05580H-(cit5a)/*[position()=1]) 2019; 119
Weiss (D0CC05580H-(cit8b)/*[position()=1]) 2011; 50
Zhao (D0CC05580H-(cit11j)/*[position()=1]) 2019; 21
Zhong (D0CC05580H-(cit4c)/*[position()=1]) 2014; 16
Liu (D0CC05580H-(cit4h)/*[position()=1]) 2019; 141
Artero (D0CC05580H-(cit7c)/*[position()=1]) 2011; 50
Yu (D0CC05580H-(cit5h)/*[position()=1]) 2019; 58
Qi (D0CC05580H-(cit3d)/*[position()=1]) 2019; 55
Lazarides (D0CC05580H-(cit7b)/*[position()=1]) 2009; 131
Chen (D0CC05580H-(cit4a)/*[position()=1]) 2018; 51
Gao (D0CC05580H-(cit4e)/*[position()=1]) 2015; 5
Zhong (D0CC05580H-(cit3b)/*[position()=1]) 2013; 19
Dempsey (D0CC05580H-(cit7a)/*[position()=1]) 2009; 42
Schrauzer (D0CC05580H-(cit6a)/*[position()=1]) 1968; 1
Uoyama (D0CC05580H-(cit12a)/*[position()=1]) 2012; 492
Lu (D0CC05580H-(cit11k)/*[position()=1]) 2020; 362
Xuan (D0CC05580H-(cit2c)/*[position()=1]) 2012; 51
He (D0CC05580H-(cit5d)/*[position()=1]) 2014; 7
Xuan (D0CC05580H-(cit11b)/*[position()=1]) 2015; 54
Staveness (D0CC05580H-(cit2g)/*[position()=1]) 2016; 49
Chen (D0CC05580H-(cit3a)/*[position()=1]) 2018; 62
Larock (D0CC05580H-(cit9b)/*[position()=1]) 1993; 58
Zhang (D0CC05580H-(cit11e)/*[position()=1]) 2017; 19
Cai (D0CC05580H-(cit2i)/*[position()=1]) 2019; 64
Penteado (D0CC05580H-(cit11a)/*[position()=1]) 2019; 119
Goddard (D0CC05580H-(cit2f)/*[position()=1]) 2016; 49
Bergonzini (D0CC05580H-(cit11d)/*[position()=1]) 2015; 54
Yoon (D0CC05580H-(cit2b)/*[position()=1]) 2010; 2
Tang (D0CC05580H-(cit5c)/*[position()=1]) 2018; 140
Zeitler (D0CC05580H-(cit2a)/*[position()=1]) 2009; 48
He (D0CC05580H-(cit5e)/*[position()=1]) 2017; 56
Tan (D0CC05580H-(cit11c)/*[position()=1]) 2015; 54
Zhong (D0CC05580H-(cit3c)/*[position()=1]) 2017; 53
Zhong (D0CC05580H-(cit3e)/*[position()=1]) 2019; 10
Sun (D0CC05580H-(cit5g)/*[position()=1]) 2018; 10
Cai (D0CC05580H-(cit3f)/*[position()=1]) 2016; 18
Meng (D0CC05580H-(cit4d)/*[position()=1]) 2013; 135
Zhang (D0CC05580H-(cit5b)/*[position()=1]) 2016; 52
Weiss (D0CC05580H-(cit8a)/*[position()=1]) 2011; 50
Prier (D0CC05580H-(cit2d)/*[position()=1]) 2013; 113
Jasperse (D0CC05580H-(cit1)/*[position()=1]) 1991; 91
Liu (D0CC05580H-(cit2h)/*[position()=1]) 2017; 4
Zhang (D0CC05580H-(cit9a)/*[position()=1]) 1992; 57
Obora (D0CC05580H-(cit10a)/*[position()=1]) 2001; 123
Zheng (D0CC05580H-(cit4g)/*[position()=1]) 2016; 138
Huang (D0CC05580H-(cit10b)/*[position()=1]) 2007; 9
Zou (D0CC05580H-(cit11h)/*[position()=1]) 2018; 360
Zhong (D0CC05580H-(cit4b)/*[position()=1]) 2017; 75
Prier, CK (WOS:000321810600018) 2013; 113
SCHRAUZE.GN (WOS:A1968B534600001) 1968; 1
Zhong, JJ (WOS:000334016600040) 2014; 16
Zhao, JJ (WOS:000459366800014) 2019; 21
Cai, SY (WOS:000378303400051) 2016; 18
Xuan, J (WOS:000305990800005) 2012; 51
Hu, JC (WOS:000499480200018) 2019; 55
Luo, MJ (WOS:000471909900025) 2019; 55
Romero, NA (WOS:000383410100011) 2016; 116
Weiss, ME (WOS:000297863900040) 2011; 50
Xuan, J (WOS:000368061800004) 2015; 54
Staveness, D (WOS:000385908100025) 2016; 49
Penteado, F (WOS:000473251600007) 2019; 119
Yoon, TP (WOS:000280078200012) 2010; 2
LAROCK, RC (WOS:A1993LB51700031) 1993; 58
Yuan, H (WOS:000424012300016) 2018; 61
Cao, H (WOS:000451933100048) 2018; 140
Huang, J (WOS:000249987200065) 2007; 9
Qi, XK (WOS:000484981000035) 2019; 55
Dempsey, JL (WOS:000273082800015) 2009; 42
Liu, WQ (WOS:000484828900036) 2019; 141
Weiss, ME (WOS:000297467100014) 2011; 50
Zeitler, K (WOS:000273452200007) 2009; 48
Artero, V (WOS:000293840400007) 2011; 50
Zhong, JJ (WOS:000395965800004) 2017; 75
ZHANG, LJ (WOS:A1992HA46600075) 1992; 57
Uoyama, H (WOS:000312259300038) 2012; 492
Yu, WL (WOS:000478635100027) 2019; 58
Lu, J (WOS:000535321000014) 2020; 362
Zheng, YW (WOS:000381715700004) 2016; 138
Zou, HX (WOS:000429346800020) 2018; 360
Zhang, GT (WOS:000382119600020) 2016; 52
Gao, XW (WOS:000352464400043) 2015; 5
Cui, L (WOS:000375891700062) 2016; 18
Meng, QY (WOS:000329137300002) 2013; 135
Liu, J (WOS:000329152600026) 2014; 53
Tang, S (WOS:000447953600001) 2018; 140
He, KH (WOS:000342815400002) 2014; 7
Genovino, J (WOS:000434367500018) 2018; 20
Bergonzini, G (WOS:000367722500040) 2015; 54
Lazarides, T (WOS:000267633300029) 2009; 131
Xuan, J (WOS:000533976700002) 2020; 49
PATTENDEN, G (WOS:A1988U143100002) 1988; 17
Tan, H (WOS:000358050300007) 2015; 54
Capaldo, L (WOS:000419751100032) 2018; 8
Chen, B (WOS:000447816000017) 2018; 51
Goddard, J. P. (000583607100041.12) 2016; 49
Sun, X (WOS:000450790300012) 2018; 10
Zhong, JJ (WOS:000407169500003) 2017; 53
He, KH (WOS:000397307600047) 2017; 56
Cai, BG (WOS:000460874700012) 2019; 64
Zhang, GT (WOS:000358896600020) 2015; 137
Zhang, ML (WOS:000405358300025) 2017; 19
Liu, Q (WOS:000406611700011) 2017; 4
Zhong, JJ (WOS:000468818700016) 2019; 10
JASPERSE, CP (WOS:A1991GJ57900006) 1991; 91
Wang, HM (WOS:000473251600001) 2019; 119
Zhong, JJ (WOS:000318365200034) 2013; 19
Obora, Y (WOS:000171860700008) 2001; 123
References_xml – volume: 51
  start-page: 6828
  year: 2012
  ident: D0CC05580H-(cit2c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201200223
– volume: 360
  start-page: 1439
  year: 2018
  ident: D0CC05580H-(cit11h)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201701567
– volume: 55
  start-page: 10848
  year: 2019
  ident: D0CC05580H-(cit3d)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC04977K
– volume: 5
  start-page: 2391
  year: 2015
  ident: D0CC05580H-(cit4e)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.5b00093
– volume: 137
  start-page: 9273
  year: 2015
  ident: D0CC05580H-(cit4f)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b05665
– volume: 52
  start-page: 10407
  year: 2016
  ident: D0CC05580H-(cit5b)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC04109D
– volume: 8
  start-page: 304
  year: 2018
  ident: D0CC05580H-(cit11f)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.7b03719
– volume: 4
  start-page: 359
  year: 2017
  ident: D0CC05580H-(cit2h)/*[position()=1]
  publication-title: Natl. Sci. Rev.
  doi: 10.1093/nsr/nwx039
– volume: 55
  start-page: 7251
  year: 2019
  ident: D0CC05580H-(cit11i)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC03210J
– volume: 49
  start-page: 1924
  year: 2016
  ident: D0CC05580H-(cit2f)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.6b00288
– volume: 116
  start-page: 10075
  year: 2016
  ident: D0CC05580H-(cit2e)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.6b00057
– volume: 17
  start-page: 361
  year: 1988
  ident: D0CC05580H-(cit6b)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/cs9881700361
– volume: 18
  start-page: 2188
  year: 2016
  ident: D0CC05580H-(cit10c)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.6b00802
– volume: 58
  start-page: 10941
  year: 2019
  ident: D0CC05580H-(cit5h)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201904707
– volume: 362
  start-page: 2178
  year: 2020
  ident: D0CC05580H-(cit11k)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.202000116
– volume: 91
  start-page: 1237
  year: 1991
  ident: D0CC05580H-(cit1)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr00006a006
– volume: 140
  start-page: 16360
  year: 2018
  ident: D0CC05580H-(cit5f)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b11218
– volume: 50
  start-page: 7238
  year: 2011
  ident: D0CC05580H-(cit7c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201007987
– volume: 138
  start-page: 10080
  year: 2016
  ident: D0CC05580H-(cit4g)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b05498
– volume: 123
  start-page: 10489
  year: 2001
  ident: D0CC05580H-(cit10a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja010674p
– volume: 119
  start-page: 6769
  year: 2019
  ident: D0CC05580H-(cit5a)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.9b00045
– volume: 119
  start-page: 7113
  year: 2019
  ident: D0CC05580H-(cit11a)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.8b00782
– volume: 2
  start-page: 527
  year: 2010
  ident: D0CC05580H-(cit2b)/*[position()=1]
  publication-title: Nat. Chem.
  doi: 10.1038/nchem.687
– volume: 54
  start-page: 15632
  year: 2015
  ident: D0CC05580H-(cit11b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201505731
– volume: 42
  start-page: 1995
  year: 2009
  ident: D0CC05580H-(cit7a)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar900253e
– volume: 1
  start-page: 97
  year: 1968
  ident: D0CC05580H-(cit6a)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar50004a001
– volume: 50
  start-page: 11501
  year: 2011
  ident: D0CC05580H-(cit8b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201104681
– volume: 492
  start-page: 234
  year: 2012
  ident: D0CC05580H-(cit12a)/*[position()=1]
  publication-title: Nature
  doi: 10.1038/nature11687
– volume: 57
  start-page: 774
  year: 1992
  ident: D0CC05580H-(cit9a)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00028a075
– volume: 16
  start-page: 1988
  year: 2014
  ident: D0CC05580H-(cit4c)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol500534w
– volume: 141
  start-page: 13941
  year: 2019
  ident: D0CC05580H-(cit4h)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b06920
– volume: 62
  start-page: 24
  year: 2018
  ident: D0CC05580H-(cit3a)/*[position()=1]
  publication-title: Sci. China: Chem.
  doi: 10.1007/s11426-018-9399-2
– volume: 7
  start-page: 2788
  year: 2014
  ident: D0CC05580H-(cit5d)/*[position()=1]
  publication-title: ChemSusChem
  doi: 10.1002/cssc.201402606
– volume: 140
  start-page: 13128
  year: 2018
  ident: D0CC05580H-(cit5c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b07327
– volume: 53
  start-page: 8948
  year: 2017
  ident: D0CC05580H-(cit3c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C7CC03823B
– volume: 20
  start-page: 3229
  year: 2018
  ident: D0CC05580H-(cit11g)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b01085
– volume: 21
  start-page: 913
  year: 2019
  ident: D0CC05580H-(cit11j)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b03840
– volume: 53
  start-page: 502
  year: 2014
  ident: D0CC05580H-(cit12b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201308614
– volume: 49
  start-page: 2295
  year: 2016
  ident: D0CC05580H-(cit2g)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.6b00270
– volume: 10
  start-page: 1229
  year: 2018
  ident: D0CC05580H-(cit5g)/*[position()=1]
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-018-0142-4
– volume: 56
  start-page: 3080
  year: 2017
  ident: D0CC05580H-(cit5e)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201612486
– volume: 51
  start-page: 2512
  year: 2018
  ident: D0CC05580H-(cit4a)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.8b00267
– volume: 113
  start-page: 5322
  year: 2013
  ident: D0CC05580H-(cit2d)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr300503r
– volume: 10
  start-page: 4883
  year: 2019
  ident: D0CC05580H-(cit3e)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C8SC05600E
– volume: 18
  start-page: 2990
  year: 2016
  ident: D0CC05580H-(cit3f)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.6b01353
– volume: 58
  start-page: 2846
  year: 1993
  ident: D0CC05580H-(cit9b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00062a031
– volume: 54
  start-page: 14066
  year: 2015
  ident: D0CC05580H-(cit11d)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201506432
– volume: 55
  start-page: 14490
  year: 2019
  ident: D0CC05580H-(cit7d)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC08512B
– volume: 54
  start-page: 8374
  year: 2015
  ident: D0CC05580H-(cit11c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201503479
– volume: 48
  start-page: 9785
  year: 2009
  ident: D0CC05580H-(cit2a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200904056
– volume: 131
  start-page: 9192
  year: 2009
  ident: D0CC05580H-(cit7b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja903044n
– volume: 19
  start-page: 6443
  year: 2013
  ident: D0CC05580H-(cit3b)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201204572
– volume: 19
  start-page: 3430
  year: 2017
  ident: D0CC05580H-(cit11e)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.7b01391
– volume: 135
  start-page: 19052
  year: 2013
  ident: D0CC05580H-(cit4d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja408486v
– volume: 9
  start-page: 4343
  year: 2007
  ident: D0CC05580H-(cit10b)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol7019839
– volume: 75
  start-page: 34
  year: 2017
  ident: D0CC05580H-(cit4b)/*[position()=1]
  publication-title: Acta Chim. Sin.
  doi: 10.6023/A16090491
– volume: 64
  start-page: 337
  year: 2019
  ident: D0CC05580H-(cit2i)/*[position()=1]
  publication-title: Sci. Bull.
  doi: 10.1016/j.scib.2019.02.002
– volume: 49
  start-page: 2546
  year: 2020
  ident: D0CC05580H-(cit2j)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00523D
– volume: 50
  start-page: 11125
  year: 2011
  ident: D0CC05580H-(cit8a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201105235
– volume: 119
  start-page: 6769
  year: 2019
  ident: WOS:000473251600001
  article-title: Recent Advances in Oxidative R-1-H/R-2-H Cross-Coupling with Hydrogen Evolution via Photo-/Electrochemistry
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.9b00045
– volume: 21
  start-page: 913
  year: 2019
  ident: WOS:000459366800014
  article-title: Enantioselective Radical Hydroacylation of Enals with alpha-Ketoacids Enabled by Photoredox/Amine Cocatalysis
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b03840
– volume: 75
  start-page: 34
  year: 2017
  ident: WOS:000395965800004
  article-title: Visible Light Induced Cross-Coupling Hydrogen Evolution Reactions
  publication-title: ACTA CHIMICA SINICA
  doi: 10.6023/A16090491
– volume: 131
  start-page: 9192
  year: 2009
  ident: WOS:000267633300029
  article-title: Making Hydrogen from Water Using a Homogeneous System Without Noble Metals
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja903044n
– volume: 50
  start-page: 7238
  year: 2011
  ident: WOS:000293840400007
  article-title: Splitting Water with Cobalt
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201007987
– volume: 53
  start-page: 8948
  year: 2017
  ident: WOS:000407169500003
  article-title: Platinum(II) photo-catalysis for highly selective difluoroalkylation reactions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c7cc03823b
– volume: 17
  start-page: 361
  year: 1988
  ident: WOS:A1988U143100002
  article-title: COBALT-MEDIATED RADICAL REACTIONS IN ORGANIC-SYNTHESIS
  publication-title: CHEMICAL SOCIETY REVIEWS
– volume: 5
  start-page: 2391
  year: 2015
  ident: WOS:000352464400043
  article-title: Visible Light Catalysis Assisted Site-Specific Functionalization of Amino Acid Derivatives by C-H Bond Activation without Oxidant: Cross-Coupling Hydrogen Evolution Reaction
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.5b00093
– volume: 119
  start-page: 7113
  year: 2019
  ident: WOS:000473251600007
  article-title: alpha-Keto Acids: Acylating Agents in Organic Synthesis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.8b00782
– volume: 9
  start-page: 4343
  year: 2007
  ident: WOS:000249987200065
  article-title: Palladium-catalyzed alpha-vinylation of carbonyl compounds
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol7019839
– volume: 19
  start-page: 3430
  year: 2017
  ident: WOS:000405358300025
  article-title: Photoredox-Catalyzed Hydroacylation of Olefins Employing Carboxylic Acids and Hydrosilanes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b01391
– volume: 58
  start-page: 2846
  year: 1993
  ident: WOS:A1993LB51700031
  article-title: SYNTHESIS AND ACYLATION OF ALLYLIC MERCURIC IODIDES - A CONVENIENT SYNTHESIS OF ALLYLIC KETONES
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 20
  start-page: 3229
  year: 2018
  ident: WOS:000434367500018
  article-title: Metal-Free-Visible Light C-H Alkylation of Heteroaromatics via Hypervalent Iodine-Promoted Decarboxylation
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b01085
– volume: 49
  start-page: 2295
  year: 2016
  ident: WOS:000385908100025
  article-title: Free Radical Chemistry Enabled by Visible Light-Induced Electron Transfer
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/acs.accounts.6b00270
– volume: 137
  start-page: 9273
  year: 2015
  ident: WOS:000358896600020
  article-title: External Oxidant-Free Oxidative Cross-Coupling: A Photoredox Cobalt-Catalyzed Aromatic C-H Thiolation for Constructing C-S Bonds
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.5b05665
– volume: 54
  start-page: 8374
  year: 2015
  ident: WOS:000358050300007
  article-title: Sunlight-Driven Decarboxylative Alkynylation of alpha-Keto Acids with Bromoacetylenes by Hypervalent Iodine Reagent Catalysis: A Facile Approach to Ynones
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201503479
– volume: 492
  start-page: 234
  year: 2012
  ident: WOS:000312259300038
  article-title: Highly efficient organic light-emitting diodes from delayed fluorescence
  publication-title: NATURE
  doi: 10.1038/nature11687
– volume: 2
  start-page: 527
  year: 2010
  ident: WOS:000280078200012
  article-title: Visible light photocatalysis as a greener approach to photochemical synthesis
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/NCHEM.687
– volume: 55
  start-page: 14490
  year: 2019
  ident: WOS:000499480200018
  article-title: A biomimetic self-assembled cobaloxime@CdS/rGO hybrid for boosting photocatalytic H-2 production
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc08512b
– volume: 61
  start-page: 243
  year: 2018
  ident: WOS:000424012300016
  article-title: Appraisal of an oligomerization behavior of unprotected carbohydrates induced by phosphorus reagent
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-017-9165-4
– volume: 50
  start-page: 11501
  year: 2011
  ident: WOS:000297863900040
  article-title: Total Synthesis of (+)-Daphmanidin E
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201104681
– volume: 362
  start-page: 2178
  year: 2020
  ident: WOS:000535321000014
  article-title: Photoredox Catalyst Free, Visible Light-Promoted C3-H Acylation of Quinoxalin-2(1H)-ones in Water
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.202000116
– volume: 42
  start-page: 1995
  year: 2009
  ident: WOS:000273082800015
  article-title: Hydrogen Evolution Catalyzed by Cobaloximes
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/ar900253e
– volume: 50
  start-page: 11125
  year: 2011
  ident: WOS:000297467100014
  article-title: Cobalt-Catalyzed Coupling of Alkyl Iodides with Alkenes: Deprotonation of Hydridocobalt Enables Turnover
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201105235
– volume: 18
  start-page: 2990
  year: 2016
  ident: WOS:000378303400051
  article-title: Visible-Light-Enabled Decarboxylative Sulfonylation of Cinnamic Acids with Sulfonylhydrazides under Transition-Metal-Free Conditions
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.6b01353
– volume: 18
  start-page: 2188
  year: 2016
  ident: WOS:000375891700062
  article-title: Silver-Catalyzed Decarboxylative Allylation of Aliphatic Carboxylic Acids in Aqueous Solution
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.6b00802
– volume: 57
  start-page: 774
  year: 1992
  ident: WOS:A1992HA46600075
  article-title: ON PENTAORGANYLSTIBORANE .2. REACTIONS OF PENTAORGANYLSTIBORANES WITH ACYL CHLORIDES AND KETONES
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 19
  start-page: 6443
  year: 2013
  ident: WOS:000318365200034
  article-title: A Highly Efficient and Selective Aerobic Cross-Dehydrogenative-Coupling Reaction Photocatalyzed by a Platinum(II) Terpyridyl Complex
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201204572
– volume: 54
  start-page: 15632
  year: 2015
  ident: WOS:000368061800004
  article-title: Visible-Light-Induced Decarboxylative Functionalization of Carboxylic Acids and Their Derivatives
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201505731
– volume: 52
  start-page: 10407
  year: 2016
  ident: WOS:000382119600020
  article-title: Visible-light induced oxidant-free oxidative cross-coupling for constructing allylic sulfones from olefins and sulfinic acids
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc04109d
– volume: 113
  start-page: 5322
  year: 2013
  ident: WOS:000321810600018
  article-title: Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr300503r
– volume: 141
  start-page: 13941
  year: 2019
  ident: WOS:000484828900036
  article-title: Cobaloxime Catalysis: Selective Synthesis of Alkenylphosphine Oxides under Visible Light
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b06920
– volume: 135
  start-page: 19052
  year: 2013
  ident: WOS:000329137300002
  article-title: A Cascade Cross-Coupling Hydrogen Evolution Reaction by Visible Light Catalysis
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja408486v
– volume: 10
  start-page: 4883
  year: 2019
  ident: WOS:000468818700016
  article-title: Efficient acceptorless photo-dehydrogenation of alcohols and N-heterocycles with binuclear platinum(ii) diphosphite complexes
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c8sc05600e
– volume: 55
  start-page: 7251
  year: 2019
  ident: WOS:000471909900025
  article-title: Decarboxylative [4+2] annulation of arylglyoxylic acids with internal alkynes using the anodic ruthenium catalysis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc03210j
– volume: 4
  start-page: 359
  year: 2017
  ident: WOS:000406611700011
  article-title: Recent advances in visible-light-driven organic reactions
  publication-title: NATIONAL SCIENCE REVIEW
  doi: 10.1093/nsr/nwx039
– volume: 64
  start-page: 337
  year: 2019
  ident: WOS:000460874700012
  article-title: Visible light-mediated C-P bond formation reactions
  publication-title: SCIENCE BULLETIN
  doi: 10.1016/j.scib.2019.02.002
– volume: 138
  start-page: 10080
  year: 2016
  ident: WOS:000381715700004
  article-title: Photocatalytic Hydrogen-Evolution Cross-Couplings: Benzene C -H Amination and Hydroxylation
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b05498
– volume: 49
  start-page: 1924
  year: 2016
  ident: 000583607100041.12
  publication-title: Acc. Chem. Res.
– volume: 51
  start-page: 2512
  year: 2018
  ident: WOS:000447816000017
  article-title: Photocatalytic Activation of Less Reactive Bonds and Their Functionalization via Hydrogen-Evolution Cross-Couplings
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/acs.accounts.8b00267
– volume: 360
  start-page: 1439
  year: 2018
  ident: WOS:000429346800020
  article-title: Silver-Catalyzed Decarboxylative Couplings of Acids and Anhydrides: An Entry to 1,2-Diketones and Aryl-Substituted Ethanes
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201701567
– volume: 7
  start-page: 2788
  year: 2014
  ident: WOS:000342815400002
  article-title: Oxidant-Free Dehydrogenative Coupling Reactions via Hydrogen Evolution
  publication-title: CHEMSUSCHEM
  doi: 10.1002/cssc.201402606
– volume: 123
  start-page: 10489
  year: 2001
  ident: WOS:000171860700008
  article-title: Palladium complex catalyzed acylation of allylic esters with acylsilanes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja010674p
– volume: 55
  start-page: 10848
  year: 2019
  ident: WOS:000484981000035
  article-title: Photoinduced synthesis of fluorinated dibenz[b,e]azepines via radical triggered cyclization
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc04977k
– volume: 140
  start-page: 13128
  year: 2018
  ident: WOS:000447953600001
  article-title: Oxidative R-1-H/R-2-H Cross-Coupling with Hydrogen Evolution
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b07327
– volume: 51
  start-page: 6828
  year: 2012
  ident: WOS:000305990800005
  article-title: Visible-Light Photoredox Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201200223
– volume: 58
  start-page: 10941
  year: 2019
  ident: WOS:000478635100027
  article-title: Dehydrogenative Silylation of Alkenes for the Synthesis of Substituted Allylsilanes by Photoredox, Hydrogen-Atom Transfer, and Cobalt Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201904707
– volume: 140
  start-page: 16360
  year: 2018
  ident: WOS:000451933100048
  article-title: Photo-induced Decarboxylative Heck-Type Coupling of Unactivated Aliphatic Acids and Terminal Alkenes in the Absence of Sacrificial Hydrogen Acceptors
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b11218
– volume: 116
  start-page: 10075
  year: 2016
  ident: WOS:000383410100011
  article-title: Organic Photoredox Catalysis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.6b00057
– volume: 54
  start-page: 14066
  year: 2015
  ident: WOS:000367722500040
  article-title: Acyl Radicals from Aromatic Carboxylic Acids by Means of Visible-Light Photoredox Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201506432
– volume: 56
  start-page: 3080
  year: 2017
  ident: WOS:000397307600047
  article-title: Acceptorless Dehydrogenation of N-Heterocycles by Merging Visible-Light Photoredox Catalysis and Cobalt Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201612486
– volume: 10
  start-page: 1229
  year: 2018
  ident: WOS:000450790300012
  article-title: Catalytic dehydrogenative decarboxyolefination of carboxylic acids
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/s41557-018-0142-4
– volume: 8
  start-page: 304
  year: 2018
  ident: WOS:000419751100032
  article-title: Acyl Radicals from Acylsilanes: Photoredox-Catalyzed Synthesis of Unsymmetrical Ketones
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.7b03719
– volume: 49
  start-page: 2546
  year: 2020
  ident: WOS:000533976700002
  article-title: Visible light-promoted ring-opening functionalization of three-membered carbo- and heterocycles
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c9cs00523d
– volume: 53
  start-page: 502
  year: 2014
  ident: WOS:000329152600026
  article-title: Visible-Light-Mediated Decarboxylation/Oxidative Amidation of alpha-Keto Acids with Amines under Mild Reaction Conditions Using O-2
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201308614
– volume: 48
  start-page: 9785
  year: 2009
  ident: WOS:000273452200007
  article-title: Photoredox Catalysis with Visible Light
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200904056
– volume: 1
  start-page: 97
  year: 1968
  ident: WOS:A1968B534600001
  article-title: ORGANOCOBALT CHEMISTRY OF VITAMIN B12 MODEL COMPOUNDS (COBALOXIMES)
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
– volume: 91
  start-page: 1237
  year: 1991
  ident: WOS:A1991GJ57900006
  article-title: RADICAL REACTIONS IN NATURAL PRODUCT SYNTHESIS
  publication-title: CHEMICAL REVIEWS
– volume: 16
  start-page: 1988
  year: 2014
  ident: WOS:000334016600040
  article-title: Cross-Coupling Hydrogen Evolution Reaction in Homogeneous Solution without Noble Metals
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol500534w
SSID ssj0000158
Score 2.496321
Snippet A photoredox/cobaloxime co-catalyzed coupling reaction of α-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime...
A photoredox/cobaloxime co-catalyzed coupling reaction of a-ketoacids and methacrylates to obtain allylic ketones is described. Without the cobaloxime...
Source Web of Science
SourceID proquest
webofscience
crossref
rsc
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 1253
SubjectTerms Alkenes
Carbonyl compounds
Catalysis
Catalysts
catalytic activity
Chemistry
Chemistry, Multidisciplinary
Decarboxylation
Dehydrogenation
Ketones
Physical Sciences
redox reactions
Science & Technology
Substrates
Title Selective photoredox decarboxylation of α-ketoacids to allylic ketones and 1,4-dicarbonyl compounds dependent on cobaloxime catalysis
URI http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000583607100041
https://www.proquest.com/docview/2452099640
https://www.proquest.com/docview/2445975125
https://www.proquest.com/docview/2524214057
Volume 56
WOS 000583607100041
WOSCitedRecordID wos000583607100041
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NbtNAEF6l6QEuiL8Kl4IW0R5QcWtn_XssJhB-hFSRCt-i9XqtRoQ4Smwp4QF4Hx6CK8_EjL1emxKhwsVK1rOO4_k8O7M7-w0hh34WeAlmidu2HJgwXgcmF5kwrUwGuAkWqxxjtsUHb3ThvI3duNf70claKovkRHzduq_kf7QKbaBX3CX7D5rVF4UG-Az6hSNoGI7X0vHHqogN5v4sLnMInmWar49TKfgyydebmfYGj6Lh0Qvb_CyLnItpWpE68NlsgwTX2AjmrlpEAKsWOSau3MAF5ptZlXCOdZdWx02x3AJXFwSSiOTr6RdMGitqVpOul6tZCER3-0k1v6v3iFVGuK4g0pmN0PPXo1wNqdAYT3k1oXvegfJ5lYUQl-a7sm18XcvFpTQ_cdVfzWhA-ApDwcDqGGHmhqbPaprJE6naPMeE6CruWu6aklwhNGAdOwxum1rukfo72zpiWAwJV19aUWS5bmCN2nGxyQW4MlzqJMZq-Z6Fk7bvDtkdQLQy6JPds-H4zfsOj1lVKFb_sYYnl4Wnbe_fPaM23NlZrsRWt6hygca3yS0Vu9CzGoh3SE_O75IbUVMy8B75pgFJW0DSK4CkeUZ_fm_BSIucKjBSBUYKoKD28y4UqYYi1VCkcLEWilRD8T65eDUcRyNTFfowBfNZYYapEA4mM2cpS4SPk-u2m9lSMEdaLHU8F-xd4GYBT0TgeaEf-gn3fB76WeoFA5vtkf4cbu8BoZaTuU7KZQjdHS_lELBn4AULkdociYcM8qx5yBOhWPCxGMts8qc6DfJUyy5q7petUgeNribKNqwmmM8AsZfnWAZ5ok-DNnA5js9lXqKMA9E8ONzuX2RcTNnAoMoge4ADfR-pJUT1-5cG2d9-YrJIM4McdnGjpTBUw-1byO1lObZB7OuIReqBIV1GsX-tp_OQ3Gxf8QPSL5alfARufJE8Vi_JL7338x8
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=Selective+photoredox+decarboxylation+of+%CE%B1-ketoacids+to+allylic+ketones+and+1%2C4-dicarbonyl+compounds+dependent+on+cobaloxime+catalysis&rft.jtitle=Chemical+communications+%28Cambridge%2C+England%29&rft.au=Zhang%2C+Hong&rft.au=Xiao%2C+Qian&rft.au=Qi%2C+Xu-Kuan&rft.au=Gao%2C+Xue-Wang&rft.date=2020-10-20&rft.issn=1359-7345&rft.eissn=1364-548X&rft.volume=56&rft.issue=83&rft.spage=12530&rft.epage=12533&rft_id=info:doi/10.1039%2FD0CC05580H&rft.externalDBID=n%2Fa&rft.externalDocID=10_1039_D0CC05580H
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1359-7345&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1359-7345&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1359-7345&client=summon