Visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN to 2-aminobenzothiazoles without photocatalyst

A simple and practical method for the synthesis of 2-aminobenzothiazoles through visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN with ambient air as an oxidant in eco-friendly bis(methoxypropy) ether at ambient temperature was developed. [Display...

Full description

Saved in:
Bibliographic Details
Published inChinese chemical letters Vol. 31; no. 7; pp. 1895 - 1898
Main Authors He, Wei-Bao, Gao, Lan-Qing, Chen, Xin-Jie, Wu, Zhi-Lin, Huang, Ying, Cao, Zhong, Xu, Xin-Hua, He, Wei-Min
Format Journal Article
LanguageEnglish
Published NEW YORK Elsevier B.V 01.07.2020
Elsevier
Department of Chemistry, Hunan University, Changsha 410082, China%School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China%School of Chemistry and Chemical Engineering,University of South China%Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology,Changsha 410114, China
Subjects
Online AccessGet full text

Cover

Loading…
Abstract A simple and practical method for the synthesis of 2-aminobenzothiazoles through visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN with ambient air as an oxidant in eco-friendly bis(methoxypropy) ether at ambient temperature was developed. [Display omitted] By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-, hazardous additive-, photocatalyst-free conditions was established.
AbstractList By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-, hazardous additive-, photocatalyst-free conditions was established. (C) 2020 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
By using ambient air as the oxidant and malic acid as the promoter,a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-,hazardous additive-,photocatalyst-free conditions was established.
A simple and practical method for the synthesis of 2-aminobenzothiazoles through visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN with ambient air as an oxidant in eco-friendly bis(methoxypropy) ether at ambient temperature was developed. [Display omitted] By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-, hazardous additive-, photocatalyst-free conditions was established.
Author He, Wei-Bao
Wu, Zhi-Lin
Gao, Lan-Qing
He, Wei-Min
Chen, Xin-Jie
Xu, Xin-Hua
Huang, Ying
Cao, Zhong
AuthorAffiliation Department of Chemistry, Hunan University, Changsha 410082, China%School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China%School of Chemistry and Chemical Engineering,University of South China%Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology,Changsha 410114, China
AuthorAffiliation_xml – name: Department of Chemistry, Hunan University, Changsha 410082, China%School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China%School of Chemistry and Chemical Engineering,University of South China%Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology,Changsha 410114, China
Author_xml – sequence: 1
  givenname: Wei-Bao
  orcidid: 0000-0002-9481-6697
  surname: He
  fullname: He, Wei-Bao
  organization: Department of Chemistry, Hunan University, Changsha 410082, China
– sequence: 2
  givenname: Lan-Qing
  surname: Gao
  fullname: Gao, Lan-Qing
  organization: Department of Chemistry, Hunan University, Changsha 410082, China
– sequence: 3
  givenname: Xin-Jie
  surname: Chen
  fullname: Chen, Xin-Jie
  organization: School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China
– sequence: 4
  givenname: Zhi-Lin
  surname: Wu
  fullname: Wu, Zhi-Lin
  organization: School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China
– sequence: 5
  givenname: Ying
  surname: Huang
  fullname: Huang, Ying
  organization: Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology, Changsha 410114, China
– sequence: 6
  givenname: Zhong
  surname: Cao
  fullname: Cao, Zhong
  organization: Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology, Changsha 410114, China
– sequence: 7
  givenname: Xin-Hua
  surname: Xu
  fullname: Xu, Xin-Hua
  email: xinhuaxu2019@yeah.net
  organization: Department of Chemistry, Hunan University, Changsha 410082, China
– sequence: 8
  givenname: Wei-Min
  surname: He
  fullname: He, Wei-Min
  email: weiminhe2016@yeah.net
  organization: Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology, Changsha 410114, China
BookMark eNqNkcuO1DAQRSM0SMwMfAGb7FigZMpxHvaCBYp4jBjBgsfWcvzoVOO2W4mbofs3-OFxulssWAArl0v3lMv3XmUXPniTZc8JlARIe7MulXImlhVUUEJVAiGPskvCOlY0vK0vUg1AClaT7kl2Nc9rgIox2l5mv77hjIMzhcPVGAv0GFFGo_ONdKhyqVAX2ylswtJTclZSm1yF3dahX92ovXJ4kBGDz4PNZRKmS8I26M2cS6_zD5_7j3kMeVUszTAYfwhxRHkILinuMY5hF_PtGGJQMkq3n-PT7LGVbjbPzud19vXtmy_9--Lu07vb_vVdoShtYlFXWpKamYoPoFtLFaMcOl6bzvL0US27Slsz0K5jDZXMStJQYhXj0PK240CvsxenuffSW-lXYh12k08visNq_Pl9WNyEDmiTlC_PSjMEOys0XhmxnXAjp70AgKZmPDmaqqOa_b-6x3j0rw87HxNKT6iawjxPxv7GCIglarEWx6jFspyASqSoE8X_oNR5apwkun-wr06sSU7_QDOJ88IaJ6Oi0AH_yj8AZ8LI6A
CitedBy_id crossref_primary_10_1039_D1QO00816A
crossref_primary_10_1016_j_cclet_2021_08_071
crossref_primary_10_1016_j_cclet_2022_03_096
crossref_primary_10_1039_D0QO01587C
crossref_primary_10_1016_j_cclet_2020_09_034
crossref_primary_10_1039_D2QO01082H
crossref_primary_10_1039_D0GC02844D
crossref_primary_10_1039_D1QO00112D
crossref_primary_10_1016_j_cclet_2020_03_007
crossref_primary_10_1039_D1RA02569D
crossref_primary_10_1021_acs_joc_3c02444
crossref_primary_10_1021_acs_orglett_4c04230
crossref_primary_10_1016_j_mcat_2023_113073
crossref_primary_10_1016_j_cclet_2021_01_018
crossref_primary_10_1016_S1872_2067_20_63750_0
crossref_primary_10_1021_acs_joc_2c01499
crossref_primary_10_1039_D3GC00716B
crossref_primary_10_1039_D2QO02019J
crossref_primary_10_1002_cjoc_202300610
crossref_primary_10_1039_D0CY02273J
crossref_primary_10_6023_cjoc202109044
crossref_primary_10_1039_D1GC00562F
crossref_primary_10_6023_cjoc202107021
crossref_primary_10_1016_j_cclet_2021_02_047
crossref_primary_10_6023_cjoc202107022
crossref_primary_10_1002_cjoc_202100787
crossref_primary_10_1039_D4OB00432A
crossref_primary_10_1016_j_cclet_2023_108183
crossref_primary_10_1002_ajoc_202200131
crossref_primary_10_1039_D2QO00311B
crossref_primary_10_1002_slct_202102903
crossref_primary_10_1016_j_cclet_2020_09_059
crossref_primary_10_1002_aoc_7934
crossref_primary_10_1016_j_cclet_2021_01_021
crossref_primary_10_1016_j_cclet_2022_01_065
crossref_primary_10_6023_cjoc202106006
crossref_primary_10_1039_D0RA07701A
crossref_primary_10_1039_D2GC01644C
crossref_primary_10_1016_S1872_2067_21_63850_0
crossref_primary_10_1021_acssuschemeng_1c06691
crossref_primary_10_1016_j_gresc_2021_03_006
crossref_primary_10_1016_j_cclet_2020_04_042
crossref_primary_10_1002_ajoc_202100694
crossref_primary_10_1039_D1RA01672E
crossref_primary_10_6023_cjoc202106001
crossref_primary_10_1021_acs_orglett_0c03853
crossref_primary_10_1016_j_cclet_2021_09_068
crossref_primary_10_1016_j_cclet_2021_09_067
crossref_primary_10_1039_D1QO00375E
crossref_primary_10_1039_D2NJ00131D
crossref_primary_10_1016_j_tetlet_2021_153257
crossref_primary_10_1016_j_cclet_2022_06_063
crossref_primary_10_1016_j_cclet_2021_08_036
crossref_primary_10_1016_j_cclet_2021_02_067
crossref_primary_10_1039_D2OB01939F
crossref_primary_10_1039_D0QO01410A
crossref_primary_10_1039_D0RA07884K
crossref_primary_10_1016_j_cclet_2024_109498
crossref_primary_10_1021_acs_jmedchem_2c01460
crossref_primary_10_1002_adsc_202100448
crossref_primary_10_1016_j_jcat_2025_116010
crossref_primary_10_6023_cjoc202112032
crossref_primary_10_1039_D2QO00539E
crossref_primary_10_3390_molecules27238461
crossref_primary_10_1039_D1RA05494E
crossref_primary_10_1021_acs_joc_0c02529
crossref_primary_10_1039_D1GC00474C
crossref_primary_10_1039_D2OB01424F
crossref_primary_10_1016_S1872_2067_21_63831_7
crossref_primary_10_1021_acs_orglett_1c00235
crossref_primary_10_1016_j_cclet_2022_02_028
crossref_primary_10_1039_D0NJ05894G
crossref_primary_10_1002_adsc_202001002
crossref_primary_10_1039_D1GC01017D
crossref_primary_10_1016_j_cclet_2021_04_037
crossref_primary_10_1002_ajoc_202300290
crossref_primary_10_1002_ejoc_202201145
crossref_primary_10_1016_j_tetlet_2023_154694
crossref_primary_10_1002_adsc_202100228
crossref_primary_10_1002_chem_202400719
crossref_primary_10_1039_D0GC02663H
crossref_primary_10_1039_D1NJ04878C
crossref_primary_10_6023_cjoc202112018
crossref_primary_10_1016_j_cclet_2023_108418
crossref_primary_10_1021_acsomega_2c01814
crossref_primary_10_1016_j_cclet_2020_11_036
crossref_primary_10_1039_D4OB00295D
crossref_primary_10_1055_a_2457_0146
crossref_primary_10_1039_D2GC00903J
crossref_primary_10_1002_adsc_202300927
crossref_primary_10_6023_cjoc202012047
crossref_primary_10_1016_j_cclet_2022_03_084
crossref_primary_10_1021_acs_joc_0c02107
crossref_primary_10_1016_j_cclet_2020_07_017
crossref_primary_10_1002_adsc_202100876
crossref_primary_10_1039_D1RA06897K
crossref_primary_10_1016_j_cclet_2022_05_079
crossref_primary_10_1039_D1RA04194K
crossref_primary_10_1002_ejoc_202300713
crossref_primary_10_1002_adsc_202300535
crossref_primary_10_1002_asia_202101139
crossref_primary_10_1016_j_cclet_2022_06_022
crossref_primary_10_1016_j_cclet_2021_06_005
Cites_doi 10.1039/C9GC02657F
10.1016/j.cclet.2019.09.041
10.1016/j.tetlet.2020.151704
10.1016/S1872-2067(19)63420-0
10.1039/C8QO01079J
10.1016/j.cclet.2019.05.063
10.1039/C9CC01995B
10.1016/S1872-2067(19)63526-6
10.1002/adsc.201801433
10.1039/C9GC03008E
10.1002/adsc.201901163
10.1039/C8QO00229K
10.1039/C9CC01332F
10.1002/ajoc.201700660
10.1039/C9CC06924K
10.1021/acs.joc.9b01643
10.1039/C6GC00516K
10.1016/j.cclet.2019.10.031
10.1039/C9OB00278B
10.1039/C9QO00091G
10.1039/C9GC03769A
10.1021/acs.orglett.9b00372
10.1039/C9GC02229E
10.1039/C9GC03713F
10.1039/C7NJ03776G
10.1002/adsc.201801122
10.6023/cjoc201904070
10.6023/cjoc202000006
10.1039/C9GC02206F
10.1016/j.cclet.2019.06.052
10.1021/acs.joc.7b01122
10.1039/C9QO01334B
10.1021/acssuschemeng.9b05715
10.1016/j.cclet.2019.05.041
10.1039/C9GC03345A
10.1002/adsc.201900984
10.1016/j.scib.2019.02.002
10.1002/adsc.201901206
10.1021/acs.joc.7b01683
10.1039/c3cs60241a
10.1016/j.cclet.2019.09.040
10.1021/acssuschemeng.9b02511
10.1039/C9GC03899J
10.1039/C9CC00469F
10.1039/C6GC01487A
10.1016/j.cclet.2019.01.033
10.1039/C6GC03323G
10.1039/C9CC05949K
10.1021/acssuschemeng.7b01102
10.1016/j.cclet.2019.04.008
10.6023/cjoc201711014
10.1021/acscatal.9b04411
10.1016/j.cclet.2018.11.024
10.1016/j.tet.2019.07.014
10.1021/acscombsci.9b00124
10.1002/slct.201903451
10.1039/c2gc36083g
10.1039/C9CC01014A
10.1021/acs.orglett.9b02921
10.6023/cjoc201900002
10.1007/s11426-019-9675-5
10.1016/j.cclet.2019.04.033
10.1016/j.cclet.2019.05.048
10.1016/j.cclet.2019.08.002
10.1016/j.cclet.2019.03.034
10.1021/acssuschemeng.8b04451
10.1016/j.tetlet.2019.06.017
10.1021/acssuschemeng.8b06445
10.1016/j.cclet.2018.05.007
10.1016/j.ejmech.2013.03.064
10.1039/C8MD00142A
10.1039/C9QO01240K
10.1002/adsc.201900643
10.1016/j.cclet.2019.07.049
10.1002/ajoc.201900382
10.1039/C9CC02232E
10.1039/c9gc00222g
10.1039/c9qo01334b
10.1039/c9gc02229e
10.1039/c9cc00469f
10.1039/c9qo01240k
10.1039/c9cc02232e
10.1039/c9qo00091g
10.1039/c6gc00516k
10.1039/c9gc03899j
10.1039/c9gc02206f
10.1039/c9cc01014a
10.1039/c6gc01487a
10.1039/c6gc03323g
10.1039/c9ob00278b
10.7503/cjcu20190448
10.1039/c9cc01995b
10.13287/j.1001-9332.202002.009
10.1039/c9gc03769a
10.1039/c9gc02657f
10.1039/c9gc03345a
10.1039/c9gc03713f
10.1039/c9gc03008e
10.1039/c8qo01079j
10.1039/c9cc05949k
10.1039/c9cc01332f
ContentType Journal Article
Copyright 2020 The Author
Copyright © Wanfang Data Co. Ltd. All Rights Reserved.
Copyright_xml – notice: 2020 The Author
– notice: Copyright © Wanfang Data Co. Ltd. All Rights Reserved.
DBID AAYXX
CITATION
17B
1KN
AOWDO
BLEPL
DTL
EGQ
2B.
4A8
92I
93N
PSX
TCJ
DOI 10.1016/j.cclet.2020.02.011
DatabaseName CrossRef
Web of Knowledge
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)
Wanfang Data Journals - Hong Kong
WANFANG Data Centre
Wanfang Data Journals
万方数据期刊 - 香港版
China Online Journals (COJ)
China Online Journals (COJ)
DatabaseTitle CrossRef
Web of Science
DatabaseTitleList 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 1878-5964
EndPage 1898
ExternalDocumentID zghxkb202007035
000548928800035
10_1016_j_cclet_2020_02_011
S1001841720300711
GrantInformation_xml – fundername: Hunan Provincial Natural Science Foundation of China; Natural Science Foundation of Hunan Province
  grantid: 2019JJ20008
– fundername: We are grateful for financial support from the Hunan Provincial Natural Science Foundation of China
  funderid: (No.2019JJ20008)
GroupedDBID --K
--M
.~1
0R~
188
1B1
1~.
1~5
29B
2B.
2C.
2WC
4.4
457
4G.
5GY
5VR
5VS
6J9
7-5
71M
8P~
8RM
92E
92I
92Q
93N
AABNK
AACTN
AAEDT
AAEDW
AAIAV
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AARLI
AAXUO
ABFNM
ABFRF
ABJNI
ABMAC
ABXDB
ABYKQ
ACDAQ
ACGFO
ACGFS
ACNNM
ACRLP
ADBBV
ADECG
ADEZE
ADMUD
AEBSH
AEFWE
AEKER
AENEX
AFKWA
AFTJW
AFUIB
AFZHZ
AGHFR
AGUBO
AGYEJ
AIEXJ
AIKHN
AITUG
AJBFU
AJOXV
AJSZI
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
AXJTR
BKOJK
BLXMC
C1A
CCEZO
CDRFL
CHBEP
CS3
CW9
DU5
EBS
EFJIC
EFLBG
EJD
EO9
EP2
EP3
F5P
FA0
FDB
FEDTE
FIRID
FLBIZ
FNPLU
FYGXN
GBLVA
GX1
HVGLF
HZ~
J1W
KOM
M41
MO0
N9A
O-L
O9-
OAUVE
OK1
OZT
P-8
P-9
P2P
PC.
Q38
RIG
ROL
RPZ
S..
SDF
SDG
SDH
SES
SPC
SPCBC
SSK
SSZ
T5K
TCJ
TGP
UNMZH
UZ4
~G-
-SB
-S~
5XA
5XC
AATTM
AAXKI
AAYWO
AAYXX
ABWVN
ACRPL
ACVFH
ADCNI
ADNMO
AEIPS
AEUPX
AFPUW
AFXIZ
AGCQF
AGRNS
AIGII
AIIUN
AKBMS
AKRWK
AKYEP
ANKPU
APXCP
BNPGV
CAJEB
CITATION
Q--
SSH
U1G
U5L
17B
1KN
BLEPL
DTL
EFKBS
GROUPED_WOS_WEB_OF_SCIENCE
4A8
PSX
ID FETCH-LOGICAL-c335t-42da148e29b0d6f3c8390794e7f9417da72dfeb377853a8fa1531fc8906967903
IEDL.DBID .~1
ISICitedReferencesCount 107
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000548928800035
ISSN 1001-8417
IngestDate Thu May 29 04:08:20 EDT 2025
Fri Aug 29 16:12:39 EDT 2025
Wed Aug 06 06:46:01 EDT 2025
Thu Apr 24 23:03:10 EDT 2025
Tue Jul 01 03:18:56 EDT 2025
Fri Feb 23 02:47:01 EST 2024
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords Cascade reaction
2-Aminobenzothiazoles
Photocatalyst-free
Air
Photocatalysis
OXIDATION
DESIGN
CATALYST-FREE
HYDROXYLATION
EFFICIENT SYNTHESIS
REDUCTIVE MINISCI REACTION
METAL
QUINOXALIN-2(1H)-ONES
DERIVATIVES
MOLECULAR-OXYGEN
Language English
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c335t-42da148e29b0d6f3c8390794e7f9417da72dfeb377853a8fa1531fc8906967903
ORCID 0000-0002-9481-6697
PageCount 4
ParticipantIDs wanfang_journals_zghxkb202007035
webofscience_primary_000548928800035CitationCount
crossref_citationtrail_10_1016_j_cclet_2020_02_011
webofscience_primary_000548928800035
elsevier_sciencedirect_doi_10_1016_j_cclet_2020_02_011
crossref_primary_10_1016_j_cclet_2020_02_011
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-07-01
PublicationDateYYYYMMDD 2020-07-01
PublicationDate_xml – month: 07
  year: 2020
  text: 2020-07-01
  day: 01
PublicationDecade 2020
PublicationPlace NEW YORK
PublicationPlace_xml – name: NEW YORK
PublicationTitle Chinese chemical letters
PublicationTitleAbbrev CHINESE CHEM LETT
PublicationTitle_FL Chinese Chemical Letters
PublicationYear 2020
Publisher Elsevier B.V
Elsevier
Department of Chemistry, Hunan University, Changsha 410082, China%School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China%School of Chemistry and Chemical Engineering,University of South China%Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology,Changsha 410114, China
Publisher_xml – name: Elsevier B.V
– name: Elsevier
– name: Department of Chemistry, Hunan University, Changsha 410082, China%School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China%School of Chemistry and Chemical Engineering,University of South China%Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation, Changsha University of Science and Technology,Changsha 410114, China
References Xia, Li, Miao, Li, Wang, Li, Chen, Wei, Cai, Xuan, Xiao, Wang, Ji, Zhao, Huang, Zhang, Chen, Li, Liu, Zhang, Wu, Zhang, Gong, Meng, Zhu, Xie, Hu, Song, Liu, Wang, Chen, Liu, Liu, Yue, Li, Yan, Gan, He, Chen, Zeng, Ou, Zou, Han, Yu, Su, Bao, Liu, Lv, Wang, Zhang, Zhang (bib0015) 2017; 19
Liu, Zeng, Zeng, Peng, Hu, Hu, Peng, Song, He, Wang, He, Peng, Hu, Tang, Jiao, Xu, He, Lin, Yu, Peng, Lin, He, Peng, Wang, Yu, Gui, He, Wang (bib0055) 2019; 30
Zhu, Bao, Ying, Zeng, Chen, He, Liu, Li, Xie, Xie, Chen, Qin, Gan, Yan, Li, Liu, Cheng, Hu, Liu, Deng, Yang (bib0005) 2018; 7
Yang, Tan, Gu, Gao, Wang, Liu, Sun, Jiang, Chen, Yang, Yu, Peng, Hu, Lu, Cao, Zhu, Lin, He, Lu, Wang, Xia, Xu, Chen, Wang (bib0030) 2012; 14
Jiang, Yu, Tang, Li, Wu (bib0050) 2017; 82
Zhu, Li, Shi, Wang, Shi, Li, Zhu, Wang, Liu, Wang, Yue, Zou, Li, Wang, Wang, Li, Yan, Gong, Dou, Yang (bib0060) 2016; 18
Catalano, Carocci, Defrenza (bib0040) 2013; 64
Xu, Li, Zhang, Fan, Salah, Abdel-Halim, Engel, Dadmal, Katre, Mandewale, Kumbhare (bib0045) 2017; 82
Gu, Jerome, Lai, Bai, Gu, Yang, Wu, Yu, Hu, Li, Dong, Zhang, Jérôme, Gu, Bao, Wang, Tang (bib0010) 2013; 42
Liu, Deng, Zeng, Xie, Lu, Ding, Dong, Li, Li, Dong, Chen, Chen, Xie, Bai, Xu (bib0020) 2020; 41
Zhang, Fu, Gao, Zhao, Li, Xie, Wang, Zhao, Li, Zhang, Wang, Han, Jin, Jiang, Yang, Fu, Xu, Li, Huang (bib0025) 2017; 5
Wang, Xiong, Jie, Yu, Cui, Du, Pi, Wan, Wu, Cui, Sun, Chen, Zhang, Wang, Zhang, Zhang, Huang, Zhu, Yi, Zhao, Wei, Gong, Li, Gan, Yang, Song, Jie, Wang, Cui, Zhang, Sun, Lv, Sun, Li, Gui, Shen, Pi, Cui, Wu, Mi, Kong, Zhang, Pi, Cui, Meng, Kang, Zhang, Min, Song, Ouyang, Li, Wu, Jiang, Song, Li, Ma, Nong, Zhao, Zhao, Liang, Nie, Zhu, Liao, Chang, Liu, Miao, Wang, Liu, Ji, Deng, Huang, Han, Li, Sun (bib0035) 2018; 29
Lu (10.1016/j.cclet.2020.02.011_sbref0030f) 2019; 30
Liu (10.1016/j.cclet.2020.02.011_sbref0015i) 2019; 361
Meng (10.1016/j.cclet.2020.02.011_sbref0035l) 2020; 22
He (10.1016/j.cclet.2020.02.011_sbref0015k) 2020
Gu (10.1016/j.cclet.2020.02.011_sbref0010a) 2013; 42
Ma (10.1016/j.cclet.2020.02.011_sbref0035o) 2020; 362
Zhang (10.1016/j.cclet.2020.02.011_sbref0025a) 2017; 5
Li (10.1016/j.cclet.2020.02.011_sbref0060e) 2019; 7
Shi (10.1016/j.cclet.2020.02.011_sbref0060b) 2016; 18
Xu (10.1016/j.cclet.2020.02.011_sbref0030g) 2020; 31
Liu (10.1016/j.cclet.2020.02.011_sbref0005c) 2019; 84
Min (10.1016/j.cclet.2020.02.011_sbref0035m) 2019; 55
Salah (10.1016/j.cclet.2020.02.011_sbref0045b) 2018; 9
Li (10.1016/j.cclet.2020.02.011_sbref0015b) 2018; 360
Xie (10.1016/j.cclet.2020.02.011_sbref0005d) 2019; 6
Wu (10.1016/j.cclet.2020.02.011_sbref0015f) 2019; 17
Gao (10.1016/j.cclet.2020.02.011_sbref0030b) 2018; 38
Peng (10.1016/j.cclet.2020.02.011_sbref0055c) 2019; 30
Peng (10.1016/j.cclet.2020.02.011_sbref0055g) 2020; 40
Xie (10.1016/j.cclet.2020.02.011_sbref0015g) 2019; 7
Peng (10.1016/j.cclet.2020.02.011_sbref0030d) 2019; 30
Bao (10.1016/j.cclet.2020.02.011_sbref0010e) 2019; 30
Du (10.1016/j.cclet.2020.02.011_sbref0035b) 2019; 361
Lai (10.1016/j.cclet.2020.02.011_sbref0010b) 2018; 6
Zhu (10.1016/j.cclet.2020.02.011_sbref0060a) 2016; 18
Wang (10.1016/j.cclet.2020.02.011_sbref0015n) 2020; 31
Liu (10.1016/j.cclet.2020.02.011_sbref0005g) 2020; 22
Han (10.1016/j.cclet.2020.02.011_sbref0025d) 2019; 21
Peng (10.1016/j.cclet.2020.02.011_sbref0055b) 2019; 361
Liu (10.1016/j.cclet.2020.02.011_sbref0060c) 2019; 21
Zou (10.1016/j.cclet.2020.02.011_sbref0060d) 2019; 55
Yang (10.1016/j.cclet.2020.02.011_sbref0010c) 2019; 7
Ou (10.1016/j.cclet.2020.02.011_sbref0015l) 2020
Xu (10.1016/j.cclet.2020.02.011_sbref0045a) 2017; 82
Han (10.1016/j.cclet.2020.02.011_sbref0035s) 2020; 61
Huang (10.1016/j.cclet.2020.02.011_sbref0035e) 2020; 31
Xie (10.1016/j.cclet.2020.02.011_sbref0020e) 2020; 22
Wu (10.1016/j.cclet.2020.02.011_sbref0035n) 2019; 55
Catalano (10.1016/j.cclet.2020.02.011_bib0040) 2013; 64
Xia (10.1016/j.cclet.2020.02.011_sbref0015a) 2017; 19
Wang (10.1016/j.cclet.2020.02.011_sbref0015d) 2019; 21
Zhao (10.1016/j.cclet.2020.02.011_sbref0035p) 2020; 22
Liu (10.1016/j.cclet.2020.02.011_sbref0055a) 2019; 30
Bao (10.1016/j.cclet.2020.02.011_sbref0015m) 2020; 7
Gong (10.1016/j.cclet.2020.02.011_sbref0035f) 2019; 8
Zhang (10.1016/j.cclet.2020.02.011_sbref0015e) 2019; 21
Zhao (10.1016/j.cclet.2020.02.011_sbref0025c) 2019; 6
Wang (10.1016/j.cclet.2020.02.011_sbref0035d) 2019; 60
Peng (10.1016/j.cclet.2020.02.011_sbref0055h) 2020; 41
Liu (10.1016/j.cclet.2020.02.011_sbref0020a) 2020
Peng (10.1016/j.cclet.2020.02.011_sbref0055e) 2019; 30
Zeng (10.1016/j.cclet.2020.02.011_sbref0005b) 2019; 6
Zhao (10.1016/j.cclet.2020.02.011_sbref0025b) 2018; 5
Xu (10.1016/j.cclet.2020.02.011_sbref0025e) 2019; 21
Zhu (10.1016/j.cclet.2020.02.011_sbref0005a) 2018; 7
Wang (10.1016/j.cclet.2020.02.011_sbref0035a) 2018; 29
Yang (10.1016/j.cclet.2020.02.011_sbref0035g) 2019; 55
Li (10.1016/j.cclet.2020.02.011_sbref0015j) 2019; 21
Liu (10.1016/j.cclet.2020.02.011_sbref0005f) 2019; 55
Cao (10.1016/j.cclet.2020.02.011_sbref0030e) 2019; 30
Sun (10.1016/j.cclet.2020.02.011_sbref0035i) 2019; 30
Shen (10.1016/j.cclet.2020.02.011_sbref0035j) 2019; 30
Jiang (10.1016/j.cclet.2020.02.011_bib0050) 2017; 82
Mi (10.1016/j.cclet.2020.02.011_sbref0035k) 2019; 30
Li (10.1016/j.cclet.2020.02.011_sbref0010d) 2019; 21
Zhang (10.1016/j.cclet.2020.02.011_sbref0035h) 2019; 30
Sun (10.1016/j.cclet.2020.02.011_sbref0030c) 2019; 75
Gan (10.1016/j.cclet.2020.02.011_sbref0005e) 2019; 361
Cai (10.1016/j.cclet.2020.02.011_sbref0015c) 2019; 64
Yang (10.1016/j.cclet.2020.02.011_sbref0030a) 2012; 14
He (10.1016/j.cclet.2020.02.011_sbref0055f) 2020; 63
Sun (10.1016/j.cclet.2020.02.011_sbref0035c) 2019; 55
Wang (10.1016/j.cclet.2020.02.011_sbref0055d) 2019; 39
Dong (10.1016/j.cclet.2020.02.011_sbref0020c) 2019; 40
Zhu (10.1016/j.cclet.2020.02.011_sbref0035q) 2020; 5
Xie (10.1016/j.cclet.2020.02.011_sbref0020b) 2020; 41
Gui (10.1016/j.cclet.2020.02.011_sbref0055i) 2020; 22
Wang (10.1016/j.cclet.2020.02.011_sbref0035r) 2020; 10
Liu (10.1016/j.cclet.2020.02.011_sbref0015h) 2019; 55
Dong (10.1016/j.cclet.2020.02.011_sbref0020d) 2019; 39
Dadmal (10.1016/j.cclet.2020.02.011_sbref0045c) 2018; 42
Shen, ZH (WOS:000474501000004) 2019; 30
Li, R (WOS:000465500000001) 2018; 360
Xie, LY (WOS:000503330400071) 2019; 7
Gu, YL (WOS:000327260500015) 2013; 42
Yang, Z (WOS:000468832200023) 2019; 55
Yang, J (WOS:000311413200012) 2012; 14
Xie, LY (WOS:000541151700002) 2020; 41
Li, MH (WOS:000483588100007) 2019; 21
Zhu, L (WOS:000507660100049) 2020; 5
Cao, G. (000548928800035.5) 2013; 38
Dong, DQ (WOS:000490625200006) 2019; 40
Gan, ZY (WOS:000483193800001) 2019; 361
He, WM (WOS:000518489100001) 2020; 63
Wang, ZZ (WOS:000490291800003) 2019; 21
Lu, LH (WOS:000474501100022) 2019; 30
Liu, QS (WOS:000494413900001) 2019; 361
Han, YZ (WOS:000461843900053) 2019; 21
Wang, Z (WOS:000518129500030) 2019; 39
Dong, DQ (WOS:000501352500017) 2019; 39
Ou, W. (000548928800035.37) 2020
Peng, S (WOS:000522786900030) 2020; 40
Daclina, T.L. (000548928800035.7) 2018; 42
Han, QQ (WOS:000527103800006) 2020; 61
Bao, WH (WOS:000506722300045) 2019; 30
Gui, QW (WOS:000505605500011) 2020; 22
Peng, LF (WOS:000482249800004) 2019; 30
Xu Li-qing (BCI:BCI202000376960) 2020; 31
Zou, L (WOS:000464325900008) 2019; 55
Liu, KJ (WOS:000509965500015) 2020; 22
Peng, LF (WOS:000506722300022) 2019; 30
Liu, Y (WOS:000489645500017) 2019; 55
Bao, PL (WOS:000511876900006) 2020; 7
Peng, S (WOS:000498419800001) 2019; 361
Wang, ZZ (WOS:000506725100018) 2020; 10
Liu, BB (WOS:000468003200013) 2019; 55
Zhu, WM (WOS:000425000600009) 2018; 7
Li, GQ (WOS:000482173100040) 2019; 7
Zhu, XJ (WOS:000389230300023) 2016; 18
Peng, S (WOS:000506722300052) 2019; 30
Zhang, M (WOS:000405139100063) 2017; 5
Liu, RZ (WOS:000487576900035) 2019; 84
Cao, Z (WOS:000506722300019) 2019; 30
Ma, XP (WOS:000499298400001) 2020; 362
Min, MY (WOS:000463755900015) 2019; 55
Zhao, LL (WOS:000454251300011) 2019; 6
Wu, J (WOS:000465615200003) 2019; 17
Xu, YT (WOS:000486309300012) 2019; 21
Zhang, M (WOS:000490659100006) 2019; 21
Wu, YC (WOS:000467979900016) 2019; 55
Catalano, A (WOS:000321230300036) 2013; 64
Liu, QS (WOS:000464318800005) 2019; 21
Peng, YY (WOS:000525762600009) 2020; 41
Zeng, FL (WOS:000466794900023) 2019; 6
Xu, XM (WOS:000509632800006) 2020; 31
Gong, XQ (WOS:000477195300001) 2019; 8
Salah, M (WOS:000436030700014) 2018; 9
Li, GQ (WOS:000489200100053) 2019; 21
Xia, D (WOS:000398146000022) 2017; 19
Xie, LY (WOS:000519903900017) 2020; 22
Sun, M (WOS:000482244700003) 2019; 75
Liu, K.J. (000548928800035.26) 2020
Yang, G.P. (000548928800035.38) 2019; 7
He, S. (000548928800035.16) 2020
Zhao, HP (WOS:000509965500011) 2020; 22
Xie, LY (WOS:000501342100005) 2019; 6
Jiang, HF (WOS:000411304500006) 2017; 82
Meng, XX (WOS:000518034000034) 2020; 22
Zhang, YL (WOS:000474501000002) 2019; 30
Lai, BB (WOS:000452344900121) 2018; 6
Cai, BG (WOS:000460874700012) 2019; 64
Shi, Q (WOS:000383999300013) 2016; 18
Sun, JN (WOS:000462106900009) 2019; 30
Wang, LL (WOS:000509632800010) 2020; 31
Liu, KJ (WOS:000506722300056) 2019; 30
Xu, YS (WOS:000411304500037) 2017; 82
Mi, X (WOS:000506722300054) 2019; 30
References_xml – volume: 7
  start-page: 337
  year: 2018
  end-page: 340
  ident: bib0005
  publication-title: Asian J. Org. Chem.
– volume: 41
  start-page: 1168
  year: 2020
  end-page: 1173
  ident: bib0020
  publication-title: Chin. Chem. Lett.
– volume: 30
  start-page: 2304
  year: 2019
  end-page: 2308
  ident: bib0055
  publication-title: Chin. Chem. Lett.
– volume: 42
  start-page: 9550
  year: 2013
  end-page: 9570
  ident: bib0010
  publication-title: Chem. Soc. Rev.
– volume: 5
  start-page: 6175
  year: 2017
  end-page: 6182
  ident: bib0025
  publication-title: ACS Sustain. Chem. Eng.
– volume: 82
  start-page: 9637
  year: 2017
  end-page: 9646
  ident: bib0045
  publication-title: J. Org. Chem.
– volume: 14
  start-page: 3304
  year: 2012
  end-page: 3317
  ident: bib0030
  publication-title: Green Chem.
– volume: 18
  start-page: 6373
  year: 2016
  end-page: 6379
  ident: bib0060
  publication-title: Green Chem.
– volume: 64
  start-page: 357
  year: 2013
  end-page: 364
  ident: bib0040
  publication-title: Eur. J. Med. Chem.
– volume: 19
  start-page: 1732
  year: 2017
  end-page: 1739
  ident: bib0015
  publication-title: Green Chem.
– volume: 29
  start-page: 907
  year: 2018
  end-page: 910
  ident: bib0035
  publication-title: Chin. Chem. Lett.
– volume: 82
  start-page: 9312
  year: 2017
  end-page: 9320
  ident: bib0050
  publication-title: J. Org. Chem.
– volume: 22
  start-page: 118
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0055i
  publication-title: Green Chem.
  doi: 10.1039/C9GC02657F
– volume: 30
  start-page: 2132
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0030e
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.09.041
– volume: 61
  start-page: 151704
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035s
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2020.151704
– volume: 40
  start-page: 1494
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0020c
  publication-title: Chin. J. Catal.
  doi: 10.1016/S1872-2067(19)63420-0
– volume: 6
  start-page: 87
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0025c
  publication-title: Org. Chem. Front.
  doi: 10.1039/C8QO01079J
– volume: 30
  start-page: 2151
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0030d
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.05.063
– volume: 55
  start-page: 4817
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0005f
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC01995B
– volume: 41
  start-page: 1168
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0020b
  publication-title: Chin. J. Catal.
  doi: 10.1016/S1872-2067(19)63526-6
– volume: 361
  start-page: 1766
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035b
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201801433
– volume: 21
  start-page: 5512
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015d
  publication-title: Green Chem.
  doi: 10.1039/C9GC03008E
– volume: 361
  start-page: 5721
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0055b
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201901163
– volume: 5
  start-page: 1689
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0025b
  publication-title: Org. Chem. Front.
  doi: 10.1039/C8QO00229K
– volume: 55
  start-page: 4371
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035n
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC01332F
– volume: 7
  start-page: 337
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0005a
  publication-title: Asian J. Org. Chem.
  doi: 10.1002/ajoc.201700660
– volume: 55
  start-page: 12615
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035c
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC06924K
– volume: 84
  start-page: 11763
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0005c
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.9b01643
– volume: 41
  start-page: 268
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0055h
  publication-title: Chem. J. Chin. Univ.
– volume: 18
  start-page: 4916
  year: 2016
  ident: 10.1016/j.cclet.2020.02.011_sbref0060b
  publication-title: Green Chem.
  doi: 10.1039/C6GC00516K
– volume: 30
  start-page: 2304
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0055a
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.10.031
– volume: 17
  start-page: 3507
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015f
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C9OB00278B
– volume: 6
  start-page: 1476
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0005b
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00091G
– volume: 22
  start-page: 1388
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035l
  publication-title: Green Chem.
  doi: 10.1039/C9GC03769A
– volume: 21
  start-page: 1799
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0025d
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00372
– volume: 21
  start-page: 4971
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0025e
  publication-title: Green Chem.
  doi: 10.1039/C9GC02229E
– volume: 22
  start-page: 433
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0005g
  publication-title: Green Chem.
  doi: 10.1039/C9GC03713F
– volume: 42
  start-page: 776
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0045c
  publication-title: New J. Chem.
  doi: 10.1039/C7NJ03776G
– volume: 360
  start-page: 4807
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0015b
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201801122
– volume: 39
  start-page: 3190
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0020d
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc201904070
– year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0020a
  publication-title: Chin. Chem. Lett.
– volume: 40
  start-page: 541
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0055g
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc202000006
– volume: 21
  start-page: 4650
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0010d
  publication-title: Green Chem.
  doi: 10.1039/C9GC02206F
– volume: 30
  start-page: 2259
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0010e
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.06.052
– volume: 82
  start-page: 9312
  year: 2017
  ident: 10.1016/j.cclet.2020.02.011_bib0050
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.7b01122
– volume: 7
  start-page: 492
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0015m
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO01334B
– volume: 7
  start-page: 19993
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015g
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.9b05715
– volume: 31
  start-page: 67
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0015n
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.05.041
– volume: 22
  start-page: 404
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035p
  publication-title: Green Chem.
  doi: 10.1039/C9GC03345A
– volume: 361
  start-page: 5277
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015i
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900984
– volume: 64
  start-page: 337
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015c
  publication-title: Sci. Bull.
  doi: 10.1016/j.scib.2019.02.002
– volume: 362
  start-page: 478
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035o
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201901206
– year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0015l
  publication-title: Chin. Chem. Lett.
– volume: 82
  start-page: 9637
  year: 2017
  ident: 10.1016/j.cclet.2020.02.011_sbref0045a
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.7b01683
– volume: 42
  start-page: 9550
  year: 2013
  ident: 10.1016/j.cclet.2020.02.011_sbref0010a
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c3cs60241a
– volume: 30
  start-page: 2295
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035k
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.09.040
– volume: 7
  start-page: 14009
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0060e
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.9b02511
– volume: 22
  start-page: 1720
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0020e
  publication-title: Green Chem.
  doi: 10.1039/C9GC03899J
– volume: 21
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0060c
  publication-title: Green Chem.
– volume: 55
  start-page: 3646
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035m
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC00469F
– volume: 18
  start-page: 6373
  year: 2016
  ident: 10.1016/j.cclet.2020.02.011_sbref0060a
  publication-title: Green Chem.
  doi: 10.1039/C6GC01487A
– volume: 30
  start-page: 1374
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035j
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.01.033
– volume: 19
  start-page: 1732
  year: 2017
  ident: 10.1016/j.cclet.2020.02.011_sbref0015a
  publication-title: Green Chem.
  doi: 10.1039/C6GC03323G
– volume: 55
  start-page: 12212
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015h
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC05949K
– volume: 5
  start-page: 6175
  year: 2017
  ident: 10.1016/j.cclet.2020.02.011_sbref0025a
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.7b01102
– volume: 30
  start-page: 1481
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0055e
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.04.008
– volume: 38
  start-page: 846
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0030b
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc201711014
– volume: 10
  start-page: 154
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035r
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b04411
– volume: 30
  start-page: 569
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035i
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2018.11.024
– volume: 75
  start-page: 130456
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0030c
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2019.07.014
– volume: 21
  start-page: 685
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015e
  publication-title: ACS Comb. Sci.
  doi: 10.1021/acscombsci.9b00124
– volume: 5
  start-page: 829
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035q
  publication-title: ChemistrySelect
  doi: 10.1002/slct.201903451
– volume: 14
  start-page: 3304
  year: 2012
  ident: 10.1016/j.cclet.2020.02.011_sbref0030a
  publication-title: Green Chem.
  doi: 10.1039/c2gc36083g
– volume: 55
  start-page: 3737
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0060d
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC01014A
– volume: 21
  start-page: 7938
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0015j
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b02921
– volume: 39
  start-page: 3594
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0055d
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc201900002
– volume: 63
  start-page: 291
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0055f
  publication-title: Sci. China Chem.
  doi: 10.1007/s11426-019-9675-5
– volume: 30
  start-page: 1237
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0030f
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.04.033
– year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0015k
  publication-title: Chin. Chem. Lett.
– volume: 31
  start-page: 49
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0030g
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.05.048
– volume: 30
  start-page: 2287
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0055c
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.08.002
– volume: 30
  start-page: 1361
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035h
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.03.034
– volume: 6
  start-page: 17076
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0010b
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.8b04451
– volume: 60
  start-page: 1845
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035d
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2019.06.017
– volume: 7
  start-page: 3727
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0010c
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.8b06445
– volume: 29
  start-page: 907
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0035a
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2018.05.007
– volume: 64
  start-page: 357
  year: 2013
  ident: 10.1016/j.cclet.2020.02.011_bib0040
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2013.03.064
– volume: 9
  start-page: 1045
  year: 2018
  ident: 10.1016/j.cclet.2020.02.011_sbref0045b
  publication-title: MedChemComm
  doi: 10.1039/C8MD00142A
– volume: 6
  start-page: 3950
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0005d
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO01240K
– volume: 361
  start-page: 4558
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0005e
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900643
– volume: 31
  start-page: 373
  year: 2020
  ident: 10.1016/j.cclet.2020.02.011_sbref0035e
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.07.049
– volume: 8
  start-page: 1472
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035f
  publication-title: Asian J. Org. Chem.
  doi: 10.1002/ajoc.201900382
– volume: 55
  start-page: 6094
  year: 2019
  ident: 10.1016/j.cclet.2020.02.011_sbref0035g
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC02232E
– volume: 38
  start-page: 346
  year: 2013
  ident: 000548928800035.5
  publication-title: Chin. J. Org. Chem
– volume: 40
  start-page: 1494
  year: 2019
  ident: WOS:000490625200006
  article-title: Visible-light-induced deoxygenative C2-sulfonylation of quinoline N-oxides with sulfinic acids for the synthesis of 2-sulfonylquinoline via radical reactions
  publication-title: CHINESE JOURNAL OF CATALYSIS
  doi: 10.1016/S1872-2067(19)63420-0
– volume: 63
  start-page: 291
  year: 2020
  ident: WOS:000518489100001
  article-title: Uranyl photocatalysis: precisely controlled oxidation of sulfides with ground-state oxygen
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-019-9675-5
– volume: 42
  start-page: 9550
  year: 2013
  ident: WOS:000327260500015
  article-title: Bio-based solvents: an emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c3cs60241a
– volume: 360
  start-page: 4807
  year: 2018
  ident: WOS:000465500000001
  article-title: A Visible-Light-Promoted Metal-Free Strategy towards Arylphosphonates: Organic-Dye-Catalyzed Phosphorylation of Arylhydrazines with Trialkylphosphites
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201801122
– volume: 75
  start-page: ARTN 130456
  year: 2019
  ident: WOS:000482244700003
  article-title: Deep eutectic solvent promoted hydrothiocyanation of alkynoates leading to Z-3-thiocyanatoacrylates
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2019.07.014
– volume: 30
  start-page: 2304
  year: 2019
  ident: WOS:000506722300056
  article-title: Solvent-dependent selective oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid under neat conditions
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.10.031
– volume: 84
  start-page: 11763
  year: 2019
  ident: WOS:000487576900035
  article-title: Tunable Synthesis of 3-Hydroxylisoquinolin-1,4-dione and Isoquinolin-1-one Enabled by Copper-Catalyzed Radical 6-endo Aza-cyclization of 2-Alkynylbenzamide
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.9b01643
– volume: 31
  start-page: 67
  year: 2020
  ident: WOS:000509632800010
  article-title: Metal-free visible-light-induced oxidative cyclization reaction of 1,6-enynes and arylsulfinic acids leading to sulfonylated benzofurans
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.05.041
– volume: 21
  start-page: 1609
  year: 2019
  ident: WOS:000464318800005
  article-title: Catalyst-free visible-light-initiated oxidative coupling of aryldiazo sulfones with thiols leading to unsymmetrical sulfoxides in air
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc00222g
– volume: 361
  start-page: 5721
  year: 2019
  ident: WOS:000498419800001
  article-title: Metal-Free C3 Hydroxylation of Quinoxalin-2(1H)-ones in Water
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201901163
– volume: 7
  start-page: 492
  year: 2020
  ident: WOS:000511876900006
  article-title: Visible-light-promoted acridine red catalyzed aerobic oxidative decarboxylative acylation of alpha-oxo-carboxylic acids with quinoxalin-2(1H)-ones
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo01334b
– volume: 362
  start-page: 478
  year: 2020
  ident: WOS:000499298400001
  article-title: Yb(OTf)(3)-Catalyzed Cycloaddition/[3,3]-Rearrangement of N-Vinyl-alpha,beta-Unsaturated Ketonitrones with Methylenecycloprop-anes: Stereoselective Synthesis of Nine-Membered Nitrogen Heterocycles
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201901206
– volume: 30
  start-page: 2259
  year: 2019
  ident: WOS:000506722300045
  article-title: Clean preparation of S-thiocarbamates with in situ generated hydroxide in 2-methyltetrahydrofuran
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.06.052
– volume: 82
  start-page: 9637
  year: 2017
  ident: WOS:000411304500037
  article-title: Metal-Free Synthesis of 2-Aminobenzothiazoles via Iodine-Catalyzed and Oxygen-Promoted Cascade Reactions of Isothiocyanatobenzenes with Amines
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.7b01683
– volume: 21
  start-page: 4971
  year: 2019
  ident: WOS:000486309300012
  article-title: Photoinduced hydroxylation of arylboronic acids with molecular oxygen under photocatalyst-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc02229e
– volume: 7
  start-page: 19993
  year: 2019
  ident: WOS:000503330400071
  article-title: Visible-Light-Initiated Cross-Dehydrogenative Coupling of Quinoxalin-2(1H)-ones and Simple Amides with Air as an Oxidant
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b05715
– volume: 30
  start-page: 1237
  year: 2019
  ident: WOS:000474501100022
  article-title: Sustainable routes for quantitative green selenocyanation of activated alkynes
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.04.033
– volume: 9
  start-page: 1045
  year: 2018
  ident: WOS:000436030700014
  article-title: Design and synthesis of conformationally constraint Dyrk1A inhibitors by creating an intramolecular H-bond involving a benzothiazole core
  publication-title: MEDCHEMCOMM
– volume: 21
  start-page: 7938
  year: 2019
  ident: WOS:000489200100053
  article-title: Photocatalyst-Free Visible-Light-Promoted C(sp(2))-S Coupling: A Strategy for the Preparation of S-Aryl Dithiocarbamates
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b02921
– volume: 42
  start-page: 776
  year: 2018
  ident: 000548928800035.7
  publication-title: New J. Chem.
– volume: 30
  start-page: 2287
  year: 2019
  ident: WOS:000506722300052
  article-title: TsCl-promoted sulfonylation of quinoline N-oxides with sodium sulfinates in water
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.08.002
– volume: 64
  start-page: 357
  year: 2013
  ident: WOS:000321230300036
  article-title: 2-Aminobenzothiazole derivatives: Search for new antifungal agents
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2013.03.064
– volume: 55
  start-page: 3646
  year: 2019
  ident: WOS:000463755900015
  article-title: Copper-catalyzed intermolecular oxidative trifluoromethyl-arylation of styrenes with NaSO2CF3 and indoles involving C-H functionalization
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc00469f
– volume: 6
  start-page: 3950
  year: 2019
  ident: WOS:000501342100005
  article-title: Visible-light-promoted direct C-H/S-H cross-coupling of quinoxalin-2(1H)-ones with thiols leading to 3-sulfenylated quinoxalin-2(1H)-ones in air
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo01240k
– volume: 7
  start-page: 337
  year: 2018
  ident: WOS:000425000600009
  article-title: TEMPO-Promoted C(sp(3))-H Hydroxylation of 2-Oxindoles at Room Temperature
  publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ajoc.201700660
– volume: 5
  start-page: 6175
  year: 2017
  ident: WOS:000405139100063
  article-title: Catalyst-Free, Visible-Light Promoted One-Pot Synthesis of Spirooxindole-Pyran Derivatives in Aqueous Ethyl Lactate
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.7b01102
– volume: 21
  start-page: 1799
  year: 2019
  ident: WOS:000461843900053
  article-title: Photocatalyst-Free Visible-Light Photoredox Dearomatization of Phenol Derivatives Containing Ketoximes: An Easy Access to Spiropyrrolines
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b00372
– volume: 55
  start-page: 6094
  year: 2019
  ident: WOS:000468832200023
  article-title: Iridium(iii)-catalysed annulation of pyrazolidinones with propiolates: a facile route to pyrazolo[1,2-a] indazoles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc02232e
– volume: 6
  start-page: 1476
  year: 2019
  ident: WOS:000466794900023
  article-title: Copper-catalyzed one-pot three-component thioamination of 1,4-naphthoquinone
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo00091g
– volume: 30
  start-page: 2151
  year: 2019
  ident: WOS:000506722300022
  article-title: DESs: Green solvents for transition metal catalyzed organic reactions
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.05.063
– volume: 39
  start-page: 3594
  year: 2019
  ident: WOS:000518129500030
  article-title: Radical Cyclization Strategy towards Indolo[1,2-a]quinolines
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201900002
– volume: 8
  start-page: 1472
  year: 2019
  ident: WOS:000477195300001
  article-title: Sulfonylacetonitriles as Building Blocks in Copper-Catalyzed Domino Reactions: An Efficient Apporach to Sulfonated Isoquinolin-1(2H)-ones
  publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ajoc.201900382
– volume: 18
  start-page: 4916
  year: 2016
  ident: WOS:000383999300013
  article-title: Decarboxylative/decarbonylative C3-acylation of indoles via photocatalysis: a simple and efficient route to 3-acylindoles
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c6gc00516k
– volume: 22
  start-page: 1720
  year: 2020
  ident: WOS:000519903900017
  article-title: Visible-light-induced decarboxylative acylation of quinoxalin-2(1H)-ones with alpha-oxo carboxylic acids under metal-, strong oxidant- and external photocatalyst-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03899j
– volume: 21
  start-page: 4650
  year: 2019
  ident: WOS:000483588100007
  article-title: Eco-efficient synthesis of 2-quinaldic acids from furfural
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc02206f
– volume: 361
  start-page: 4558
  year: 2019
  ident: WOS:000483193800001
  article-title: Copper-Catalyzed Domino Synthesis of Sulfur-Containing Heterocycles Using Carbon Disulfide as a Building Block
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201900643
– volume: 55
  start-page: 3737
  year: 2019
  ident: WOS:000464325900008
  article-title: Visible-light-induced Pd-catalyzed ortho-trifluoromethylation of acetanilides with CF3SO2Na under ambient conditions in the absence of an external photocatalyst
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc01014a
– volume: 18
  start-page: 6373
  year: 2016
  ident: WOS:000389230300023
  article-title: Thiyl radical catalyzed oxidation of diarylalkynes to alpha-diketones by molecular oxygen under visible-light irradiation
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c6gc01487a
– volume: 30
  start-page: 1374
  year: 2019
  ident: WOS:000474501000004
  article-title: Rhodium(III)-catalyzed intermolecular cyclization of anilines with sulfoxonium ylides toward indoles
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.01.033
– volume: 19
  start-page: 1732
  year: 2017
  ident: WOS:000398146000022
  article-title: Visible-light-induced dual C-C bond formation via selective C(sp(3))-H bond cleavage: efficient access to alkylated oxindoles from activated alkenes and simple ethers under metal-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c6gc03323g
– volume: 17
  start-page: 3507
  year: 2019
  ident: WOS:000465615200003
  article-title: Visible-light promoted aerobic difunctionalization of alkenes with sulfonyl hydrazides for the synthesis of beta-keto/hydroxyl sulfones
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c9ob00278b
– volume: 5
  start-page: 829
  year: 2020
  ident: WOS:000507660100049
  article-title: A Novel Fluorescent Probe for Detection of Hydrogen Sulfide and Its Bioimaging Applications in Living Cells
  publication-title: CHEMISTRYSELECT
  doi: 10.1002/slct.201903451
– volume: 31
  start-page: 49
  year: 2020
  ident: WOS:000509632800006
  article-title: Recent advances in sulfenylation of C(sp(3))-H bond under transition metal-free conditions
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.05.048
– year: 2020
  ident: 000548928800035.16
  publication-title: Chin. Chem. Lett.
– volume: 41
  start-page: 268
  year: 2020
  ident: WOS:000525762600009
  article-title: Rapid and Sensitive Detection of L-Cysteine Based on Mono(6-mercapto-6-deoxy)-beta-cyclodextrin Modified Gold Electrode
  publication-title: CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE
  doi: 10.7503/cjcu20190448
– year: 2020
  ident: 000548928800035.26
  publication-title: Chin. Chem. Lett.
– volume: 55
  start-page: 4817
  year: 2019
  ident: WOS:000468003200013
  article-title: Iron-catalyzed oxidative C-C(vinyl) sigma-bond cleavage of allylarenes to aryl aldehydes at room temperature with ambient air
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc01995b
– volume: 31
  start-page: 373
  year: 2020
  ident: BCI:BCI202000376960
  article-title: Root architecture and fine root characteristics of Juglans mandshurica saplings in different habitats in the secondary forest on the west slope of Zhangguangcailing, China
  publication-title: Yingyong Shengtai Xuebao
  doi: 10.13287/j.1001-9332.202002.009
– volume: 7
  start-page: 14009
  year: 2019
  ident: WOS:000482173100040
  article-title: Photocatalyst-Free Regioselective C-H Thiocyanation of 4-Anilinocoumarins under Visible Light
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b02511
– volume: 61
  start-page: ARTN 151704
  year: 2020
  ident: WOS:000527103800006
  article-title: Silver-catalyzed cascade radical cyclization of sodium sulfinates and o-(allyloxy)arylaldehydes towards functionalized chroman-4-ones
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2020.151704
– volume: 39
  start-page: 3190
  year: 2019
  ident: WOS:000501352500017
  article-title: Direct Synthesis of Sulfonated or Sulfenylated Pyrazolones Mediated by KIO3 and Their Anti -microbial Activity
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201904070
– volume: 22
  start-page: 1388
  year: 2020
  ident: WOS:000518034000034
  article-title: Visible-light-initiated regioselective sulfonylation/cyclization of 1,6-enynes under photocatalyst- and additive-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03769a
– volume: 30
  start-page: 2295
  year: 2019
  ident: WOS:000506722300054
  article-title: Visible-light-promoted sulfonylmethylation of imidazopyridines
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.09.040
– volume: 22
  start-page: 118
  year: 2020
  ident: WOS:000505605500011
  article-title: The clean preparation of multisubstituted pyrroles under metal- and solvent-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc02657f
– volume: 30
  start-page: 1361
  year: 2019
  ident: WOS:000474501000002
  article-title: Recent applications of radical cascade reaction in the synthesis of functionalized 1-indenones
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.03.034
– volume: 82
  start-page: 9312
  year: 2017
  ident: WOS:000411304500006
  article-title: Copper-Catalyzed Aerobic Oxidative Regioselective Thiocyanation of Aromatics and Heteroaromatics
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.7b01122
– volume: 14
  start-page: 3304
  year: 2012
  ident: WOS:000311413200012
  article-title: Lactic acid as an invaluable bio-based solvent for organic reactions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c2gc36083g
– volume: 30
  start-page: 2132
  year: 2019
  ident: WOS:000506722300019
  article-title: The concept of dual roles design in clean organic preparation
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.09.041
– 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: 22
  start-page: 404
  year: 2020
  ident: WOS:000509965500011
  article-title: Metal-free graphene oxide-catalyzed aza-semipinacol rearrangement to prepare 2-(indol-2-yl)phenols and benzofuro[3,2-b]indolines containing quaternary carbon centers
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03345a
– volume: 22
  start-page: 433
  year: 2020
  ident: WOS:000509965500015
  article-title: Selective oxidation of (hetero)sulfides with molecular oxygen under clean conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03713f
– volume: 21
  start-page: 5512
  year: 2019
  ident: WOS:000490291800003
  article-title: Visible-light-mediated photoredox decarbonylative Minisci-type alkylation with aldehydes under ambient air conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03008e
– volume: 7
  start-page: 3727
  year: 2019
  ident: 000548928800035.38
  publication-title: ACS Sustain. Chem. Eng.
– year: 2020
  ident: 000548928800035.37
  publication-title: Chin. Chem. Lett.
– volume: 10
  start-page: 154
  year: 2020
  ident: WOS:000506725100018
  article-title: Bromide-Promoted Visible-Light-Induced Reductive Minisci Reaction with Aldehydes
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b04411
– volume: 361
  start-page: 5277
  year: 2019
  ident: WOS:000494413900001
  article-title: Photocatalyst-Free Visible Light-Induced Synthesis of beta-Oxo Sulfones via Oxysulfonylation of Alkenes with Arylazo Sulfones and Dioxygen in Air
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201900984
– volume: 6
  start-page: 17076
  year: 2018
  ident: WOS:000452344900121
  article-title: Lignosulfonate/Dicationic Ionic Liquid Composite as a Task-Specific Catalyst Support for Enabling Efficient Synthesis of Unsymmetrical 1,3-Diynes with A Low Substrate Ratio
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.8b04451
– volume: 41
  start-page: 1168
  year: 2020
  ident: WOS:000541151700002
  article-title: C(sp(2))-H/O-H cross-dehydrogenative coupling of quinoxalin-2(1H)-ones with alcohols under visible-light photoredox catalysis
  publication-title: CHINESE JOURNAL OF CATALYSIS
  doi: 10.1016/S1872-2067(19)63526-6
– volume: 40
  start-page: 541
  year: 2020
  ident: WOS:000522786900030
  article-title: Visible Light-Induced Aldehyde Reductive Minisci Reaction towards N-Heterocycles
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc202000006
– volume: 30
  start-page: 1481
  year: 2019
  ident: WOS:000482249800004
  article-title: Recent progress in transition metal catalyzed cross coupling of nitroarenes
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.04.008
– volume: 6
  start-page: 87
  year: 2019
  ident: WOS:000454251300011
  article-title: Photoinduced synthesis of -trifluoromethylated ketones through the oxidative trifluoromethylation of styrenes using CF3SO2Na as a trifluoromethyl reagent without an external photoredox catalyst
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c8qo01079j
– volume: 55
  start-page: 12212
  year: 2019
  ident: WOS:000489645500017
  article-title: Visible-light promoted one-pot synthesis of sulfonated spiro[4,5]trienones from propiolamides, anilines and sulfur dioxide under transition metal-free conditions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc05949k
– volume: 21
  start-page: 685
  year: 2019
  ident: WOS:000490659100006
  article-title: Visible-Light-Initiated One-Pot, Three-Component Synthesis of 2-Amino-4H-pyran-3,5-dicarbonitrile Derivatives
  publication-title: ACS COMBINATORIAL SCIENCE
  doi: 10.1021/acscombsci.9b00124
– volume: 30
  start-page: 569
  year: 2019
  ident: WOS:000462106900009
  article-title: Copper(II)-catalyzed enantioselective conjugate addition of nitro esters to 2-enoyl-pyridine N-oxides
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2018.11.024
– volume: 55
  start-page: 4371
  year: 2019
  ident: WOS:000467979900016
  article-title: A metal- and oxidizing- reagent- free anodic para- selective amination of anilines with phenothiazines
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc01332f
SSID ssj0028836
Score 2.5214694
Snippet A simple and practical method for the synthesis of 2-aminobenzothiazoles through visible-light-initiated malic acid-promoted cascade coupling/cyclization of...
By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through...
By using ambient air as the oxidant and malic acid as the promoter,a practical method for the preparation of 2-aminobenzothiazoles through...
Source Web of Science
SourceID wanfang
webofscience
crossref
elsevier
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 1895
SubjectTerms 2-Aminobenzothiazoles
Air
Cascade reaction
Chemistry
Chemistry, Multidisciplinary
Photocatalysis
Photocatalyst-free
Physical Sciences
Science & Technology
Title Visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN to 2-aminobenzothiazoles without photocatalyst
URI https://dx.doi.org/10.1016/j.cclet.2020.02.011
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000548928800035
https://d.wanfangdata.com.cn/periodical/zghxkb202007035
Volume 31
WOS 000548928800035
WOSCitedRecordID wos000548928800035
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB5VRQguiKdYKJUPPRLWeSfHKmq1ULGXUtSb5fixDWyTFZtV2z3wJ_qHO-N1ViBBhTjGmkSWZzwzjr_5BuDApllsQm4Cg4eBINF43ClMqNEZxhh9qWW3I9P5PM0mZ8mn8_R8B6qhFoZgld73b3y689Z-ZOxXc7xomvEpsQcVSUj3iBQoXQV7kpOVf_i5hXlQM11XYUTQIZIemIccxkvhxwhQGXFH3BmGf4tOD69ka2U7-2N4cqHo-Ck88TkkO9xM8xnsmPY5PKqG1m0v4PZrg5Y-N8Hc0YQ0BBDCnFKzS8y6FZOq0cHC4fBwTMklYeSZ6lZUnTsbqxs199WZrLNMoiDRujJ5SRB5JlvNTk6rKes7FgU02NWmXaPGG7kmeihG_3a7Vc8WF13fuf9DN8v-JZwdH32pJoHvvhCoOE77IIm0xLOSicqa68zGClMpjrvX5LbEddQyj7TFo3ieY8SXhZXoO0OripJnZZaXPH4Fu23XmtfAkpTrOkXXKmOJXzSSSPWy2mLqYhWP7AiiYdWF8tTk1CFjLgYM2jfhVCVIVYJHAlU1gvfblxYbZo77xbNBneI3AxMYO-5_kXnlC7-9l2I9u7j-XpMQecx0BAe_WsV2Oi4hLkq0QXdjO4LwX8QqvwJEStC_-d9pv4XH9LRBFu_Bbv9jZd5h_tTX-26D7MODw48nk-kd-z0aWg
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LTxsxELZQUEUvVZ9q-vSBY61437tHtAIFArkAFTfL60dYGnajZqOW_I3-YWYcb1SkFlW9eseW5bHnsf78DSH7NkkjE3DDDCQDLNaQ7uQm0GAMI_C-WLLbkemcTdPxZXxylVztkLJ_C4OwSm_7NzbdWWvfMvKrOVrU9egc2YPyOMB7RHSUkALtIjtVMiC7B8eT8XSbd-W5qxSI8gw79ORDDualYDzEVIbccXcGwd8c1JMfsrGymf3RQzlvdPScPPNhJD3YzPQF2THNS7JX9tXbXpFfX2vY7HPD5o4ppEaMEISVmt5C4K2oVLVmCwfFgzYllwiTp6pd4QPd2Ujdqbl_oElbSyUIIrMrlbeIkqey0XRyXk5p19KQYWNbmWYNSq_lGhmiKP7ebVcdXVy3Xet-Ed0tu9fk8ujwohwzX4CBqShKOhaHWkK6ZMKi4jq1kYJoisMBNpktYB21zEJtIRvPMnD6MrcSzGdgVV7wtEizgkdvyKBpG_OW0DjhukrAuspIwohGIq9eWlmIXqzioR2SsF91oTw7ORbJmIsehnYjnKoEqkrwUICqhuTLttNiQ87xuHjaq1M82GMC3MfjHalXvvAnfCnWs-uf3yoUQqOZDMn-77tiOx0XE-cF7EF3aTskwb-IlX4FkJege_e_0_5M9sYXZ6fi9Hg6eU-e4pcN0PgDGXTfV-YjhFNd9ckfl3uTAR0L
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=Visible-light-initiated+malic+acid-promoted+cascade+coupling%2Fcyclization+of+aromatic+amines+and+KSCN+to+2-aminobenzothiazoles+without+photocatalyst&rft.jtitle=Chinese+chemical+letters&rft.au=He%2C+Wei-Bao&rft.au=Gao%2C+Lan-Qing&rft.au=Chen%2C+Xin-Jie&rft.au=Wu%2C+Zhi-Lin&rft.date=2020-07-01&rft.pub=Elsevier&rft.issn=1001-8417&rft.eissn=1878-5964&rft.volume=31&rft.issue=7&rft.spage=1895&rft.epage=1898&rft_id=info:doi/10.1016%2Fj.cclet.2020.02.011&rft.externalDBID=n%2Fa&rft.externalDocID=000548928800035
thumbnail_s http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fwww.wanfangdata.com.cn%2Fimages%2FPeriodicalImages%2Fzghxkb%2Fzghxkb.jpg