Transition-metal-free sulfonylations of methylthiolated alkynones to synthesize 3-sulfonylated thioflavones

A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions. The features of this procedure included metal-free reac...

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Published inNew journal of chemistry Vol. 44; no. 35; pp. 14786 - 1479
Main Authors Feng, Zhi-Wen, Li, Jing, Jiang, Yu-Qin, Tian, Yu, Xu, Gui-Qing, Shi, Xin, Ding, Qing-Jie, Li, Wei, Ma, Chun-Hua, Yu, Bing
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 21.09.2020
Royal Society of Chemistry
Subjects
Chemical reactions
Chemistry
Chemistry, Multidisciplinary
Crystallography
Functional groups
Hydrazides
Physical Sciences
Reagents
Science & Technology
Transition metals
QUINOLINE N-OXIDES
PHOSPHORYLATION
INDUCED DEOXYGENATIVE C2-SULFONYLATION
RADICAL CYCLIZATION
CASCADE
IONIC LIQUID
INHIBITORS
ARYLHYDRAZINES
DERIVATIVES
C-H
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Abstract A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions. The features of this procedure included metal-free reaction conditions, ease of reagent handling, short reaction times, and a broad functional group tolerance. A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions.
AbstractList A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions. The features of this procedure included metal-free reaction conditions, ease of reagent handling, short reaction times, and a broad functional group tolerance.
A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions. The features of this procedure included metal-free reaction conditions, ease of reagent handling, short reaction times, and a broad functional group tolerance. A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by which various 3-sulfonylated thioflavones were prepared under mild reaction conditions.
Author Shi, Xin
Feng, Zhi-Wen
Jiang, Yu-Qin
Li, Wei
Ma, Chun-Hua
Xu, Gui-Qing
Yu, Bing
Li, Jing
Tian, Yu
Ding, Qing-Jie
AuthorAffiliation Henan Engineering Laboratory of Chemical Pharmaceutical and Biomedical Materials
Ministry of Education
Henan Normal University
Collaborative Innovation Centre of Henan Province for Green Manufacturing of Fine Chemicals
Green Catalysis Centre, College of Chemistry
Key Laboratory of Green Chemical Media and Reactions
Henan Engineering Research Centre of Chiral Hydroxyl Pharmaceutical
School of Chemistry and Chemical Engineering
Zhengzhou University
AuthorAffiliation_xml – name: Zhengzhou University
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– name: Ministry of Education
– name: Henan Engineering Laboratory of Chemical Pharmaceutical and Biomedical Materials
– name: Collaborative Innovation Centre of Henan Province for Green Manufacturing of Fine Chemicals
– name: Key Laboratory of Green Chemical Media and Reactions
– name: Henan Normal University
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Cites_doi 10.1016/S1872-2067(19)63420-0
10.1016/j.mcat.2019.02.019
10.1021/acs.joc.8b02175
10.1016/j.tetlet.2019.02.039
10.1039/c9cc00727j
10.1002/adsc.201801122
10.1021/acs.orglett.9b00465
10.1016/j.cclet.2019.05.041
10.1021/acssuschemeng.9b00708
10.1021/acs.orglett.9b02161
10.1002/cctc.202000244
10.1002/adsc.201900544
10.1021/acs.orglett.9b00023
10.1021/acs.orglett.9b02921
10.1039/c9nj03692j
10.1021/acs.joc.8b02897
10.1039/b911852g
10.1002/adsc.201701630
10.1002/cssc.201902817
10.1039/c9cc03789f
10.1039/c8cc10243k
10.1021/acs.orglett.8b02733
10.1039/d0qo00222d
10.1039/c8cc07735e
10.1002/adsc.201900691
10.1039/c9cc01047e
10.1039/c9qo00091g
10.6023/cjoc201900002
10.1002/chem.201901025
10.1021/acs.joc.7b02718
10.1016/j.bmc.2004.02.002
10.1021/acs.orglett.8b01238
10.1002/adsc.201900643
10.1021/acs.orglett.9b00907
10.1002/adsc.201701194
10.1039/c7gc02304a
10.1039/c9ob00278b
10.1039/c7qo00478h
10.1039/b801860j
10.6023/cjoc201504039
10.1021/acs.orglett.9b01175
10.1016/j.ymssp.2019.106247
10.1016/j.cclet.2020.02.040
10.1021/acssuschemeng.9b02511
10.1021/acs.orglett.8b01278
10.1002/adfm.202001588
10.1021/acs.orglett.8b02231
10.1039/c9gc01175g
10.1021/acssuschemeng.8b06445
10.1002/adsc.202000233
10.1016/j.cclet.2019.07.053
10.1016/j.cclet.2019.03.034
10.1039/d0nj00825g
10.1002/ejoc.201900169
10.1039/c8nj06282j
10.1039/c9qo00367c
10.1039/c6sc05093j
10.1039/c8cc09250h
10.1021/acs.joc.9b00451
10.1021/acscatal.8b02194
10.1016/j.tetlet.2018.12.016
10.1016/j.tetlet.2016.12.058
10.1039/c9cc06924k
10.1021/acs.joc.8b02844
10.1021/jm020878w
10.1039/c8cc07434h
10.1002/anie.200906340
10.1021/acs.orglett.8b03508
10.1002/adsc.201900063
10.1021/acs.joc.9b00552
10.1039/c9qo00715f
10.1002/ejoc.201901581
10.1039/C6SC05093J
10.1039/C7QO00478H
10.1021/jm00205a010
10.1039/C8CC07735E
10.1039/C9CC00727J
10.1039/C7GC02304A
10.1039/C9NJ03692J
10.1002/jhet.5570210138
10.1039/C9NJ02833A
10.1039/C9QO00715F
10.1016/S0960-894X(98)00666-0
10.1039/C8CC07434H
10.1039/C9QO00367C
10.1039/C9GC01175G
10.1039/C9CC03789F
10.1039/C9CC06924K
10.1039/C8CC10243K
10.1039/D0NJ00825G
10.1021/jm960008c
10.1039/C8CC09250H
10.1002/jhet.5570220625
10.1039/C9OB00278B
10.1039/D0QO00222D
10.1039/C9QO00091G
10.1021/jm00139a017
10.1039/C9CC01047E
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Issue 35
Keywords QUINOLINE N-OXIDES
PHOSPHORYLATION
INDUCED DEOXYGENATIVE C2-SULFONYLATION
RADICAL CYCLIZATION
CASCADE
IONIC LIQUID
INHIBITORS
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C-H
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1953609
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10.1039/d0nj03386c
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Royal Society of Chemistry
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References Wang, GD (WOS:000468001500009) 2019; 6
Zhu, JW (WOS:000413826400012) 2017; 4
Li, R (WOS:000465500000001) 2018; 360
Ge, QQ (WOS:000474796800032) 2019; 84
RAZDAN, RK (WOS:A1978FD60600010) 1978; 21
Liu, XC (WOS:000502174900001) 2020; 13
HOLSHOUSER, MH (WOS:A1981LU64400016) 1981; 24
Song, TT (WOS:000463127100007) 2019; 60
Shang, TY (WOS:000468369900001) 2019; 55
Mi, PB (WOS:000481979100022) 2019; 21
Dhanak, D (WOS:000077848100047) 1998; 8
Dong, DQ (WOS:000490625200006) 2019; 40
Zhou, F (WOS:000460731900016) 2019; 55
NAKAZUMI, H (WOS:A1985AZK3300025) 1985; 22
Gan, ZY (WOS:000483193800001) 2019; 361
Wei, W (WOS:000444527000048) 2018; 20
Wang, Z (WOS:000518129500030) 2019; 39
Wan, JP (WOS:000471040700007) 2019; 25
Tian, LH (WOS:000522532300001) 2020; 12
Huang, X (WOS:000439761100003) 2018; 83
Nielsen, M (WOS:000276780500006) 2010; 49
Huang, XQ (WOS:000434367500041) 2018; 20
Sun, K (WOS:000449443100017) 2018; 20
Xu, J (WOS:000459366800056) 2019; 21
Ye, SQ (WOS:000458544800001) 2019; 55
Kitani, S (WOS:000255425800003) 2008
Li, GQ (WOS:000482173100040) 2019; 7
Kataoka, T (WOS:000221159800036) 2004; 12
Jiang, YQ (WOS:000530885000001) 2020; 362
Hu, F (WOS:000364618100004) 2015; 35
Sun, K (WOS:000481008100001) 2019; 361
He, WX (WOS:000489689600014) 2019; 133
Song, Y (WOS:000527915100010) 2020; 31
Li, HY (WOS:000397560500014) 2017; 8
Miao, CX (WOS:000468967000007) 2019; 2019
Liu, W (WOS:000453243600021) 2018; 54
Li, R (WOS:000483534400037) 2019; 43
Wang, JC (WOS:000461843900067) 2019; 21
Wu, J (WOS:000465615200003) 2019; 17
Liu, Y (WOS:000471212100032) 2019; 21
Fu, R (WOS:000471326000009) 2019; 361
Wu, C (WOS:000467351200083) 2019; 7
Zhao, JF (WOS:000431487200005) 2018; 360
Wang, HK (WOS:A1996UM24800009) 1996; 39
Yang, WC (WOS:000432900200080) 2018; 20
Lin, Y (WOS:000536157700051) 2020; 44
Sun, K (WOS:000452929900018) 2018; 83
Sun, K (WOS:000490779100002) 2019; 55
Wang, L (WOS:000618541800068) 2021; 32
Zeng, FL (WOS:000466794900023) 2019; 6
Ren, XH (WOS:000474796800031) 2019; 84
Li, HY (WOS:000444364800052) 2018; 8
Yang, FL (WOS:000393264100001) 2017; 58
Xie, LY (WOS:000475506200013) 2019; 21
Li, GQ (WOS:000489200100053) 2019; 21
Wang, SJ (WOS:000534077500001) 2020; 30
Rao, WH (WOS:000465644300085) 2019; 21
Yuan, XY (WOS:000548414700011) 2020; 7
Xie, LY (WOS:000417758700014) 2017; 19
Yang, GP (WOS:000459367400011) 2019; 7
Liu, XC (WOS:000482071700007) 2019; 361
Zhang, YL (WOS:000474501000002) 2019; 30
Qiu, GYS (WOS:000449274400002) 2018; 54
Wu, YC (WOS:000477076000018) 2019; 55
Zhang, TS (WOS:000484262900019) 2019; 6
Yang, GP (WOS:000463293300011) 2019; 468
Sun, K (WOS:000460683700028) 2019; 55
Bao, PL (WOS:000460491600055) 2019; 84
Zhu, J (WOS:000424093900001) 2018; 360
Bao, PL (WOS:000456353000002) 2019; 60
Wang, LL (WOS:000509632800010) 2020; 31
Alba, ANR (WOS:000278046100012) 2010; 39
Zhou, Y (WOS:000459738600023) 2019; 43
NAKAZUMI, H (WOS:A1984SP09700038) 1984; 21
Guo, YH (WOS:000460491600056) 2019; 84
Nussbaumer, P (WOS:000177913500022) 2002; 45
Sangeetha, S (WOS:000455285800017) 2019; 21
Li (D0NJ03386C-(cit4i)/*[position()=1]) 2019; 21
Yuan (D0NJ03386C-(cit10c)/*[position()=1]) 2020; 7
Liu (D0NJ03386C-(cit13)/*[position()=1]) 2018; 54
Holshouser (D0NJ03386C-(cit1d)/*[position()=1]) 1981; 24
Wang (D0NJ03386C-(cit8e)/*[position()=1]) 2019; 39
Li (D0NJ03386C-(cit12b)/*[position()=1]) 2018; 360
Ye (D0NJ03386C-(cit4c)/*[position()=1]) 2019; 55
Dong (D0NJ03386C-(cit7a)/*[position()=1]) 2019; 40
Rao (D0NJ03386C-(cit7o)/*[position()=1]) 2019; 21
Xie (D0NJ03386C-(cit7l)/*[position()=1]) 2019; 21
Tian (D0NJ03386C-(cit7t)/*[position()=1]) 2020; 12
Zeng (D0NJ03386C-(cit4k)/*[position()=1]) 2019; 6
Guo (D0NJ03386C-(cit7u)/*[position()=1]) 2019; 84
Sun (D0NJ03386C-(cit12c)/*[position()=1]) 2019; 55
Ge (D0NJ03386C-(cit7b)/*[position()=1]) 2019; 84
Xiong (D0NJ03386C-(cit12a)/*[position()=1]) 2020
Huang (D0NJ03386C-(cit4f)/*[position()=1]) 2018; 20
Sun (D0NJ03386C-(cit7j)/*[position()=1]) 2018; 20
Sun (D0NJ03386C-(cit8b)/*[position()=1]) 2018; 83
Zhu (D0NJ03386C-(cit8d)/*[position()=1]) 2017; 4
Nakazumi (D0NJ03386C-(cit2b)/*[position()=1]) 1985; 22
Hu (D0NJ03386C-(cit7s)/*[position()=1]) 2015; 35
Zhu (D0NJ03386C-(cit5a)/*[position()=1]) 2018; 360
Yang (D0NJ03386C-(cit8a)/*[position()=1]) 2017; 58
Wu (D0NJ03386C-(cit7n)/*[position()=1]) 2019; 17
Ren (D0NJ03386C-(cit4a)/*[position()=1]) 2019; 84
Nakazumi (D0NJ03386C-(cit1c)/*[position()=1]) 1984; 21
Huang (D0NJ03386C-(cit4b)/*[position()=1]) 2018; 83
Zhang (D0NJ03386C-(cit7g)/*[position()=1]) 2019; 6
Zhou (D0NJ03386C-(cit11b)/*[position()=1]) 2019; 55
Gan (D0NJ03386C-(cit4h)/*[position()=1]) 2019; 361
Yang (D0NJ03386C-(cit9f)/*[position()=1]) 2019; 468
Miao (D0NJ03386C-(cit4e)/*[position()=1]) 2019
Song (D0NJ03386C-(cit7p)/*[position()=1]) 2019; 60
Song (D0NJ03386C-(cit9e)/*[position()=1]) 2020; 31
Nussbaumer (D0NJ03386C-(cit1a)/*[position()=1]) 2002; 45
Jiang (D0NJ03386C-(cit8f)/*[position()=1]) 2020; 362
Wang (D0NJ03386C-(cit11a)/*[position()=1]) 2019; 21
Li (D0NJ03386C-(cit7f)/*[position()=1]) 2019
Wu (D0NJ03386C-(cit7k)/*[position()=1]) 2019; 55
Liu (D0NJ03386C-(cit12e)/*[position()=1]) 2019; 43
Alba (D0NJ03386C-(cit6a)/*[position()=1]) 2010; 39
Li (D0NJ03386C-(cit7d)/*[position()=1]) 2017; 8
Yang (D0NJ03386C-(cit9g)/*[position()=1]) 2019; 7
Liu (D0NJ03386C-(cit10b)/*[position()=1]) 2020; 13
Zhang (D0NJ03386C-(cit9c)/*[position()=1]) 2019; 30
Wan (D0NJ03386C-(cit12f)/*[position()=1]) 2019; 25
Wang (D0NJ03386C-(cit5d)/*[position()=1]) 2020; 31
Wang (D0NJ03386C-(cit2a)/*[position()=1]) 1996; 39
Sangeetha (D0NJ03386C-(cit1e)/*[position()=1]) 2019; 21
Sun (D0NJ03386C-(cit9b)/*[position()=1]) 2019; 361
Kataoka (D0NJ03386C-(cit1b)/*[position()=1]) 2004; 12
Xie (D0NJ03386C-(cit7r)/*[position()=1]) 2017; 19
Xu (D0NJ03386C-(cit10d)/*[position()=1]) 2019; 21
Bao (D0NJ03386C-(cit7h)/*[position()=1]) 2019; 60
Bao (D0NJ03386C-(cit7q)/*[position()=1]) 2019; 84
Li (D0NJ03386C-(cit12d)/*[position()=1]) 2019; 43
Kitani (D0NJ03386C-(cit3a)/*[position()=1]) 2008
Dhanak (D0NJ03386C-(cit3b)/*[position()=1]) 1998; 8
Razdan (D0NJ03386C-(cit2c)/*[position()=1]) 1978; 21
Liu (D0NJ03386C-(cit4j)/*[position()=1]) 2019; 21
Wu (D0NJ03386C-(cit5c)/*[position()=1]) 2019; 7
Shang (D0NJ03386C-(cit9d)/*[position()=1]) 2019; 55
Wei (D0NJ03386C-(cit4d)/*[position()=1]) 2018; 20
Qiu (D0NJ03386C-(cit5e)/*[position()=1]) 2018; 54
Mi (D0NJ03386C-(cit3c)/*[position()=1]) 2019; 21
Yang (D0NJ03386C-(cit5b)/*[position()=1]) 2018; 20
Nielsen (D0NJ03386C-(cit6b)/*[position()=1]) 2010; 49
Sun (D0NJ03386C-(cit8c)/*[position()=1]) 2019; 55
Li (D0NJ03386C-(cit4g)/*[position()=1]) 2019; 7
Liu (D0NJ03386C-(cit9a)/*[position()=1]) 2019; 361
Zhao (D0NJ03386C-(cit7i)/*[position()=1]) 2018; 360
Li (D0NJ03386C-(cit7e)/*[position()=1]) 2018; 8
Wang (D0NJ03386C-(cit7m)/*[position()=1]) 2019; 6
Lin (D0NJ03386C-(cit12g)/*[position()=1]) 2020; 44
Fu (D0NJ03386C-(cit7c)/*[position()=1]) 2019; 361
Wang (D0NJ03386C-(cit10a)/*[position()=1]) 2020
References_xml – 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
  contributor:
    fullname: Dong, DQ
– volume: 468
  start-page: 80
  year: 2019
  ident: WOS:000463293300011
  article-title: Non-corrosive heteropolyacid-based recyclable ionic liquid catalyzed direct dehydrative coupling of alcohols with alcohols or alkenes
  publication-title: MOLECULAR CATALYSIS
  doi: 10.1016/j.mcat.2019.02.019
  contributor:
    fullname: Yang, GP
– volume: 83
  start-page: 14419
  year: 2018
  ident: WOS:000452929900018
  article-title: Copper-Catalyzed Radical Cascade Cyclization To Access 3-Sulfonated Indenones with the AIE Phenomenon
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.8b02175
  contributor:
    fullname: Sun, K
– volume: 60
  start-page: 916
  year: 2019
  ident: WOS:000463127100007
  article-title: Gold/photoredox-cocatalyzed atom transfer thiosulfonylation of alkynes: Stereoselective synthesis of vinylsulfones
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2019.02.039
  contributor:
    fullname: Song, TT
– volume: 55
  start-page: 3117
  year: 2019
  ident: WOS:000460731900016
  article-title: A visible light photoredox catalyzed carbon radical-mediated generation of ortho-quinone methides for 2,3-dihydrobenzofuran synthesis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc00727j
  contributor:
    fullname: Zhou, F
– 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
  contributor:
    fullname: Li, R
– volume: 21
  start-page: 1863
  year: 2019
  ident: WOS:000461843900067
  article-title: An External-Catalyst-Free Trifluoromethylation/Cyclization Strategy To Access Trifluoromethylated-Dihydroisoquinolinones/Indolines with Togni Reagent II
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b00465
  contributor:
    fullname: Wang, JC
– 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
  contributor:
    fullname: Wang, LL
– volume: 7
  start-page: 8798
  year: 2019
  ident: WOS:000467351200083
  article-title: Practical Approach for Clean Preparation of Z-beta-Thiocyanate Alkenyl Esters
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b00708
  contributor:
    fullname: Wu, C
– volume: 21
  start-page: 6280
  year: 2019
  ident: WOS:000481979100022
  article-title: A Novel Fluorescent Skeleton from Disubstituted Thiochromenones via Nickel-Catalyzed Cycloaddition of Sulfobenzoic Anhydrides with Alkynes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b02161
  contributor:
    fullname: Mi, PB
– volume: 12
  start-page: 2533
  year: 2020
  ident: WOS:000522532300001
  article-title: Transition Metal-free C-H Sulfonylation and Pyrazole Annulation Cascade for the Synthesis of 4-Sulfonyl Pyrazoles
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.202000244
  contributor:
    fullname: Tian, LH
– volume: 361
  start-page: 3712
  year: 2019
  ident: WOS:000482071700007
  article-title: Visible-Light-Promoted Transition-Metal-Free Approach toward Phosphoryl-Substituted Dihydroisoquinolones via Cascade Phosphorylation/Cyclization of N-Allylbenzamides
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201900544
  contributor:
    fullname: Liu, XC
– volume: 22
  start-page: 1593
  year: 1985
  ident: WOS:A1985AZK3300025
  article-title: ANTIMICROBIAL ACTIVITY OF 3-(SUBSTITUTED METHYL)-2-PHENYL-4H-1-BENZOTHIOPYRAN-4-ONES
  publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY
  contributor:
    fullname: NAKAZUMI, H
– volume: 21
  start-page: 1112
  year: 2019
  ident: WOS:000459366800056
  article-title: Radical Promoted C(sp(2))-S Formation and C(sp(3))-S Bond Cleavage: Access to 2-Substituted Thiochromones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b00023
  contributor:
    fullname: Xu, J
– 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
  contributor:
    fullname: Li, GQ
– volume: 43
  start-page: 13642
  year: 2019
  ident: WOS:000483534400037
  article-title: Visible-light-promoted organic dye-catalyzed sulfidation and phosphorylation of arylhydrazines toward aromatic sulfides and diarylphosphoryl hydrazides
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c9nj03692j
  contributor:
    fullname: Li, R
– volume: 84
  start-page: 2984
  year: 2019
  ident: WOS:000460491600056
  article-title: Domino C-H Sulfonylation and Pyrazole Annulation for Fully Substituted Pyrazole Synthesis in Water Using Hydrophilic Enaminones
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.8b02897
  contributor:
    fullname: Guo, YH
– volume: 39
  start-page: 2018
  year: 2010
  ident: WOS:000278046100012
  article-title: Sulfones: new reagents in organocatalysis
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/b911852g
  contributor:
    fullname: Alba, ANR
– volume: 360
  start-page: 1775
  year: 2018
  ident: WOS:000431487200005
  article-title: Iron-Catalyzed Ring-Opening/Allylation of Cyclobutanone Oxime Esters with Allylic Sulfones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201701630
  contributor:
    fullname: Zhao, JF
– volume: 13
  start-page: 298
  year: 2020
  ident: WOS:000502174900001
  article-title: Visible-Light-Induced Metal-Free Synthesis of 2-Phosphorylated Thioflavones in Water
  publication-title: CHEMSUSCHEM
  doi: 10.1002/cssc.201902817
  contributor:
    fullname: Liu, XC
– volume: 55
  start-page: 8995
  year: 2019
  ident: WOS:000477076000018
  article-title: Transition-metal- and oxidant-free directed anodic C-H sulfonylation of N,N-disubstituted anilines with sulfinates
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc03789f
  contributor:
    fullname: Wu, YC
– volume: 55
  start-page: 2861
  year: 2019
  ident: WOS:000460683700028
  article-title: Silver-catalyzed decarboxylative radical cascade cyclization toward benzimidazo[2,1-a]isoquinolin-6(5H)-ones
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc10243k
  contributor:
    fullname: Sun, K
– volume: 20
  start-page: 6687
  year: 2018
  ident: WOS:000449443100017
  article-title: Synthesis of (E)-beta-Selenovinyl Sulfones through a Multicomponent Regio- and Stereospecific Selenosulfonation of Alkynes with Insertion of Sulfur Dioxide
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b02733
  contributor:
    fullname: Sun, K
– volume: 7
  start-page: 1884
  year: 2020
  ident: WOS:000548414700011
  article-title: A metal-free visible-light-promoted phosphorylation/cyclization reaction in water towards 3-phosphorylated benzothiophenes
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/d0qo00222d
  contributor:
    fullname: Yuan, XY
– volume: 54
  start-page: 14148
  year: 2018
  ident: WOS:000453243600021
  article-title: Direct synthesis of 3-acylbenzothiophenes via the radical cyclization of 2-alkynylthioanisoles with -oxocarboxylic acids
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc07735e
  contributor:
    fullname: Liu, W
– volume: 361
  start-page: 4483
  year: 2019
  ident: WOS:000481008100001
  article-title: Silver-Catalyzed Radical Cascade Cyclization of Unactivated Alkenes towards Cyclopenta[c]quinolines
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201900691
  contributor:
    fullname: Sun, K
– volume: 55
  start-page: 5408
  year: 2019
  ident: WOS:000468369900001
  article-title: Recent advances of 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) in photocatalytic transformations
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc01047e
  contributor:
    fullname: Shang, TY
– 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
  contributor:
    fullname: Zeng, FL
– 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
  contributor:
    fullname: Wang, Z
– volume: 25
  start-page: 6907
  year: 2019
  ident: WOS:000471040700007
  article-title: Transient and Recyclable Halogenation Coupling (TRHC) for Isoflavonoid Synthesis with Site-Selective Arylation
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201901025
  contributor:
    fullname: Wan, JP
– volume: 83
  start-page: 7331
  year: 2018
  ident: WOS:000439761100003
  article-title: Cobalt-Catalyzed Aerobic Cross-Dehydrogenative Coupling of C-H and Thiols in Water for C-S Formation
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.7b02718
  contributor:
    fullname: Huang, X
– volume: 12
  start-page: 2397
  year: 2004
  ident: WOS:000221159800036
  article-title: Synthesis and structure-activity relationships of thioflavone derivatives as specific inhibitors of the ERK-MAP kinase signaling pathway
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2004.02.002
  contributor:
    fullname: Kataoka, T
– volume: 20
  start-page: 3332
  year: 2018
  ident: WOS:000434367500041
  article-title: AIBN-Promoted Synthesis of Bibenzo[b][1,4]thiazines by the Condensation of 2,2'-Dithiodianiline with Methyl Aryl Ketones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b01238
  contributor:
    fullname: Huang, XQ
– 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
  contributor:
    fullname: Gan, ZY
– volume: 21
  start-page: 2890
  year: 2019
  ident: WOS:000465644300085
  article-title: Copper(II)-Catalyzed Alkene Aminosulfonylation with Sodium Sulfinates For the Synthesis of Sulfonylated Pyrrolidones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b00907
  contributor:
    fullname: Rao, WH
– volume: 360
  start-page: 386
  year: 2018
  ident: WOS:000424093900001
  article-title: Photoredox Catalysis in C-S Bond Construction: Recent Progress in Photo-Catalyzed Formation of Sulfones and Sulfoxides
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201701194
  contributor:
    fullname: Zhu, J
– volume: 19
  start-page: 5642
  year: 2017
  ident: WOS:000417758700014
  article-title: A base-free, ultrasound accelerated one-pot synthesis of 2-sulfonylquinolines in water
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c7gc02304a
  contributor:
    fullname: Xie, LY
– volume: 21
  start-page: 193
  year: 1984
  ident: WOS:A1984SP09700038
  article-title: SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 2-PHENYL-4H-BENZO[B]THIOPYRAN-4-ONES (THIOFLAVONES) AND RELATED-COMPOUNDS
  publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY
  contributor:
    fullname: NAKAZUMI, H
– 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
  contributor:
    fullname: Wu, J
– volume: 4
  start-page: 2153
  year: 2017
  ident: WOS:000413826400012
  article-title: Copper-catalyzed radical 1,2-cyclization of indoles with arylsulfonyl hydrazides: access to 2-thiolated 3H-pyrrolo[1,2-a]indoles
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c7qo00478h
  contributor:
    fullname: Zhu, JW
– start-page: 2103
  year: 2008
  ident: WOS:000255425800003
  article-title: Synthesis and characterization of thiochromone S,S-dioxides as new photolabile protecting groups
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b801860j
  contributor:
    fullname: Kitani, S
– volume: 35
  start-page: 1848
  year: 2015
  ident: WOS:000364618100004
  article-title: Progress in Iodine-Mediated Sulfonylation Reactions
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201504039
  contributor:
    fullname: Hu, F
– volume: 39
  start-page: 1975
  year: 1996
  ident: WOS:A1996UM24800009
  article-title: Antitumor agents .166. Synthesis and biological evaluation of 5,6,7,8-substituted-2-phenylthiochromen-4-ones
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  contributor:
    fullname: Wang, HK
– volume: 21
  start-page: 4019
  year: 2019
  ident: WOS:000471212100032
  article-title: Visible-Light Induced Radical Perfluoroalkylation/Cyclization Strategy To Access 2-Perfluoroalkylbenzothiazoles/Benzoselenazoles by EDA Complex
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b01175
  contributor:
    fullname: Liu, Y
– volume: 133
  start-page: ARTN 106247
  year: 2019
  ident: WOS:000489689600014
  article-title: A novel structural reliability analysis method via improved maximum entropy method based on nonlinear mapping and sparse grid numerical integration
  publication-title: MECHANICAL SYSTEMS AND SIGNAL PROCESSING
  doi: 10.1016/j.ymssp.2019.106247
  contributor:
    fullname: He, WX
– volume: 32
  start-page: 389
  year: 2021
  ident: WOS:000618541800068
  article-title: Facile syntheses of 3-trifluoromethylthio substituted thioflavones and benzothiophenes via the radical cyclization
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2020.02.040
  contributor:
    fullname: Wang, L
– 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
  contributor:
    fullname: Li, GQ
– volume: 20
  start-page: 3144
  year: 2018
  ident: WOS:000432900200080
  article-title: Cascade C(sp(3))-S Bond Cleavage and Imidoyl C-S Formation: Radical Cyclization of 2-Isocyanoaryl Thioethers toward 2-Substituted Benzothiazoles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b01278
  contributor:
    fullname: Yang, WC
– volume: 30
  start-page: ARTN 2001588
  year: 2020
  ident: WOS:000534077500001
  article-title: A Stable Conversion and Alloying Anode for Potassium-Ion Batteries: A Combined Strategy of Encapsulation and Confinement
  publication-title: ADVANCED FUNCTIONAL MATERIALS
  doi: 10.1002/adfm.202001588
  contributor:
    fullname: Wang, SJ
– volume: 20
  start-page: 5291
  year: 2018
  ident: WOS:000444527000048
  article-title: Visible-Light-Enabled Construction of Thiocarbamates from Isocyanides, Thiols, and Water at Room Temperature
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b02231
  contributor:
    fullname: Wei, W
– volume: 21
  start-page: 3858
  year: 2019
  ident: WOS:000475506200013
  article-title: Visible-light-induced deoxygenative C2-sulfonylation of quinoline N-oxides with sulfinic acids
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc01175g
  contributor:
    fullname: Xie, LY
– volume: 7
  start-page: 3727
  year: 2019
  ident: WOS:000459367400011
  article-title: Ionic Liquid from Vitamin B1 Analogue and Heteropolyacid: A Recyclable Heterogeneous Catalyst for Dehydrative Coupling in Organic Carbonate
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.8b06445
  contributor:
    fullname: Yang, GP
– volume: 362
  start-page: 2609
  year: 2020
  ident: WOS:000530885000001
  article-title: Ethylene Glycol: A Green Solvent for Visible Light-Promoted Aerobic Transition Metal-Free Cascade Sulfonation/Cyclization Reaction
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.202000233
  contributor:
    fullname: Jiang, YQ
– volume: 31
  start-page: 667
  year: 2020
  ident: WOS:000527915100010
  article-title: Protic ionic liquid-promoted synthesis of dimethyl carbonate from ethylene carbonate and methanol
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.07.053
  contributor:
    fullname: Song, Y
– 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
  contributor:
    fullname: Zhang, YL
– volume: 44
  start-page: 8120
  year: 2020
  ident: WOS:000536157700051
  article-title: Synthesis of 3-halochromones with simple KX halogen sources enabled by in situ halide oxidation
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/d0nj00825g
  contributor:
    fullname: Lin, Y
– volume: 2019
  start-page: 3012
  year: 2019
  ident: WOS:000468967000007
  article-title: Efficient Thiolation of Alcohols Catalyzed by Long Chained Acid-Functionalized Ionic Liquids under Mild Conditions
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201900169
  contributor:
    fullname: Miao, CX
– volume: 43
  start-page: 3829
  year: 2019
  ident: WOS:000459738600023
  article-title: Synthesis and electrochromic properties of a graphene oxide/silicon dioxide/oligoaniline interpenetrating network composite
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c8nj06282j
  contributor:
    fullname: Zhou, Y
– volume: 6
  start-page: 1608
  year: 2019
  ident: WOS:000468001500009
  article-title: Palladium-catalyzed direct C-H nitration and intramolecular C-H functionalization for the synthesis of 3-nitro-1-(phenylsulfonyl)-1H-indazole derivatives
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo00367c
  contributor:
    fullname: Wang, GD
– volume: 8
  start-page: 2610
  year: 2017
  ident: WOS:000397560500014
  article-title: Dual gold and photoredox catalysis: visible light-mediated intermolecular atom transfer thiosulfonylation of alkenes
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c6sc05093j
  contributor:
    fullname: Li, HY
– volume: 55
  start-page: 1013
  year: 2019
  ident: WOS:000458544800001
  article-title: Inorganic sulfites as the sulfur dioxide surrogates in sulfonylation reactions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc09250h
  contributor:
    fullname: Ye, SQ
– volume: 84
  start-page: 8683
  year: 2019
  ident: WOS:000474796800031
  article-title: Surfactant-Type Catalyst for Aerobic Oxidative Coupling of Hydrazine with Thiol in Water
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.9b00451
  contributor:
    fullname: Ren, XH
– volume: 8
  start-page: 8237
  year: 2018
  ident: WOS:000444364800052
  article-title: Atom Transfer Radical Addition to Alkynes and Enynes: A Versatile Gold/Photoredox Approach to Thio-Functionalized Vinylsulfones
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.8b02194
  contributor:
    fullname: Li, HY
– volume: 60
  start-page: 214
  year: 2019
  ident: WOS:000456353000002
  article-title: Direct coupling of haloquinolines and sulfonyl chlorides leading to sulfonylated quinolines in water
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2018.12.016
  contributor:
    fullname: Bao, PL
– volume: 21
  start-page: 643
  year: 1978
  ident: WOS:A1978FD60600010
  article-title: NEW CLASS OF ANTI-MALARIAL DRUGS - DERIVATIVES OF BENZOTHIOPYRANS
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  contributor:
    fullname: RAZDAN, RK
– volume: 58
  start-page: 487
  year: 2017
  ident: WOS:000393264100001
  article-title: Sulfonyl hydrazides as sulfonyl sources in organic synthesis
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2016.12.058
  contributor:
    fullname: Yang, FL
– volume: 24
  start-page: 853
  year: 1981
  ident: WOS:A1981LU64400016
  article-title: SYNTHESIS AND ANTI-TUMOR ACTIVITY OF A SERIES OF SULFONE ANALOGS OF 1,4-NAPHTHOQUINONE
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  contributor:
    fullname: HOLSHOUSER, MH
– volume: 55
  start-page: 12615
  year: 2019
  ident: WOS:000490779100002
  article-title: Metal-free sulfonyl radical-initiated cascade cyclization to access sulfonated indolo[1,2-a]quinolines
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc06924k
  contributor:
    fullname: Sun, K
– volume: 84
  start-page: 2976
  year: 2019
  ident: WOS:000460491600055
  article-title: Metal-Free Catalytic Synthesis of Thiocarbamates Using Sodium Sulfinates as the Sulfur Source
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.8b02844
  contributor:
    fullname: Bao, PL
– volume: 45
  start-page: 4310
  year: 2002
  ident: WOS:000177913500022
  article-title: 2-substituted 4-(thio)chromerione 6-O-sulfamates: Potent inhibitors of human steroid sulfatase
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm020878w
  contributor:
    fullname: Nussbaumer, P
– volume: 54
  start-page: 12561
  year: 2018
  ident: WOS:000449274400002
  article-title: Recent advances in the sulfonylation of C-H bonds with the insertion of sulfur dioxide
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc07434h
  contributor:
    fullname: Qiu, GYS
– volume: 49
  start-page: 2668
  year: 2010
  ident: WOS:000276780500006
  article-title: Asymmetric Organocatalysis with Sulfones
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200906340
  contributor:
    fullname: Nielsen, M
– volume: 21
  start-page: 75
  year: 2019
  ident: WOS:000455285800017
  article-title: Copper-Catalyzed One-Pot Synthesis of 2-Arylthiochromenones: An in Situ Recycle of Waste Byproduct as Useful Reagent
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b03508
  contributor:
    fullname: Sangeetha, S
– volume: 361
  start-page: 2280
  year: 2019
  ident: WOS:000471326000009
  article-title: Synthesis of 3,4-Dihydrobenzo[f]phthalazines via Iodine/tert-Butyl Hydroperoxide-Mediated Annulation Cascade of Yne-Allenones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201900063
  contributor:
    fullname: Fu, R
– volume: 84
  start-page: 8691
  year: 2019
  ident: WOS:000474796800032
  article-title: Electron Donor-Acceptor Complex Enabled Decarboxylative Sulfonylation of Cinnamic Acids under Visible-Light Irradiation
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.9b00552
  contributor:
    fullname: Ge, QQ
– volume: 8
  start-page: 3677
  year: 1998
  ident: WOS:000077848100047
  article-title: Benzothiopyran-4-one based reversible inhibitors of the human cytomegalovirus (HCMV) protease
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  contributor:
    fullname: Dhanak, D
– volume: 6
  start-page: 2968
  year: 2019
  ident: WOS:000484262900019
  article-title: Silver-catalyzed nitration/annulation of 2-alkynylanilines for a tunable synthesis of nitrated indoles and indazole-2-oxides
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo00715f
  contributor:
    fullname: Zhang, TS
– volume: 83
  start-page: 7331
  year: 2018
  ident: D0NJ03386C-(cit4b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.7b02718
  contributor:
    fullname: Huang
– volume: 84
  start-page: 8691
  year: 2019
  ident: D0NJ03386C-(cit7b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.9b00552
  contributor:
    fullname: Ge
– volume: 20
  start-page: 5291
  year: 2018
  ident: D0NJ03386C-(cit4d)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b02231
  contributor:
    fullname: Wei
– volume: 7
  start-page: 8798
  year: 2019
  ident: D0NJ03386C-(cit5c)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.9b00708
  contributor:
    fullname: Wu
– start-page: 1588
  year: 2020
  ident: D0NJ03386C-(cit12a)/*[position()=1]
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201901581
  contributor:
    fullname: Xiong
– volume: 8
  start-page: 2610
  year: 2017
  ident: D0NJ03386C-(cit7d)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C6SC05093J
  contributor:
    fullname: Li
– start-page: 2103
  year: 2008
  ident: D0NJ03386C-(cit3a)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/b801860j
  contributor:
    fullname: Kitani
– volume: 4
  start-page: 2153
  year: 2017
  ident: D0NJ03386C-(cit8d)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C7QO00478H
  contributor:
    fullname: Zhu
– volume: 21
  start-page: 4019
  year: 2019
  ident: D0NJ03386C-(cit4j)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b01175
  contributor:
    fullname: Liu
– volume: 8
  start-page: 8237
  year: 2018
  ident: D0NJ03386C-(cit7e)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.8b02194
  contributor:
    fullname: Li
– volume: 21
  start-page: 1863
  year: 2019
  ident: D0NJ03386C-(cit11a)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00465
  contributor:
    fullname: Wang
– volume: 360
  start-page: 386
  year: 2018
  ident: D0NJ03386C-(cit5a)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201701194
  contributor:
    fullname: Zhu
– volume: 39
  start-page: 2018
  year: 2010
  ident: D0NJ03386C-(cit6a)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b911852g
  contributor:
    fullname: Alba
– year: 2020
  ident: D0NJ03386C-(cit10a)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2020.02.040
  contributor:
    fullname: Wang
– volume: 21
  start-page: 643
  year: 1978
  ident: D0NJ03386C-(cit2c)/*[position()=1]
  publication-title: J. Med. Chem.
  doi: 10.1021/jm00205a010
  contributor:
    fullname: Razdan
– volume: 30
  start-page: 1361
  year: 2019
  ident: D0NJ03386C-(cit9c)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.03.034
  contributor:
    fullname: Zhang
– volume: 54
  start-page: 14148
  year: 2018
  ident: D0NJ03386C-(cit13)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC07735E
  contributor:
    fullname: Liu
– start-page: 3012
  year: 2019
  ident: D0NJ03386C-(cit4e)/*[position()=1]
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201900169
  contributor:
    fullname: Miao
– volume: 55
  start-page: 3117
  year: 2019
  ident: D0NJ03386C-(cit11b)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC00727J
  contributor:
    fullname: Zhou
– volume: 19
  start-page: 5642
  year: 2017
  ident: D0NJ03386C-(cit7r)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C7GC02304A
  contributor:
    fullname: Xie
– volume: 43
  start-page: 13642
  year: 2019
  ident: D0NJ03386C-(cit12d)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/C9NJ03692J
  contributor:
    fullname: Li
– volume: 21
  start-page: 193
  year: 1984
  ident: D0NJ03386C-(cit1c)/*[position()=1]
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.5570210138
  contributor:
    fullname: Nakazumi
– start-page: 3313
  year: 2019
  ident: D0NJ03386C-(cit7f)/*[position()=1]
  publication-title: Synthesis
  contributor:
    fullname: Li
– volume: 43
  start-page: 12221
  year: 2019
  ident: D0NJ03386C-(cit12e)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/C9NJ02833A
  contributor:
    fullname: Liu
– volume: 25
  start-page: 6907
  year: 2019
  ident: D0NJ03386C-(cit12f)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201901025
  contributor:
    fullname: Wan
– volume: 40
  start-page: 1494
  year: 2019
  ident: D0NJ03386C-(cit7a)/*[position()=1]
  publication-title: Chin. J. Catal.
  doi: 10.1016/S1872-2067(19)63420-0
  contributor:
    fullname: Dong
– volume: 12
  start-page: 2533
  year: 2020
  ident: D0NJ03386C-(cit7t)/*[position()=1]
  publication-title: ChemCatChem
  doi: 10.1002/cctc.202000244
  contributor:
    fullname: Tian
– volume: 20
  start-page: 3332
  year: 2018
  ident: D0NJ03386C-(cit4f)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b01238
  contributor:
    fullname: Huang
– volume: 7
  start-page: 3727
  year: 2019
  ident: D0NJ03386C-(cit9g)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.8b06445
  contributor:
    fullname: Yang
– volume: 84
  start-page: 2976
  year: 2019
  ident: D0NJ03386C-(cit7q)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b02844
  contributor:
    fullname: Bao
– volume: 84
  start-page: 2984
  year: 2019
  ident: D0NJ03386C-(cit7u)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b02897
  contributor:
    fullname: Guo
– volume: 21
  start-page: 6280
  year: 2019
  ident: D0NJ03386C-(cit3c)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b02161
  contributor:
    fullname: Mi
– volume: 6
  start-page: 2968
  year: 2019
  ident: D0NJ03386C-(cit7g)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00715F
  contributor:
    fullname: Zhang
– volume: 49
  start-page: 2668
  year: 2010
  ident: D0NJ03386C-(cit6b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200906340
  contributor:
    fullname: Nielsen
– volume: 39
  start-page: 3594
  year: 2019
  ident: D0NJ03386C-(cit8e)/*[position()=1]
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc201900002
  contributor:
    fullname: Wang
– volume: 60
  start-page: 214
  year: 2019
  ident: D0NJ03386C-(cit7h)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2018.12.016
  contributor:
    fullname: Bao
– volume: 13
  start-page: 298
  year: 2020
  ident: D0NJ03386C-(cit10b)/*[position()=1]
  publication-title: ChemSusChem
  doi: 10.1002/cssc.201902817
  contributor:
    fullname: Liu
– volume: 8
  start-page: 3677
  year: 1998
  ident: D0NJ03386C-(cit3b)/*[position()=1]
  publication-title: Bioorg. Med. Chem. Lett.
  doi: 10.1016/S0960-894X(98)00666-0
  contributor:
    fullname: Dhanak
– volume: 54
  start-page: 12561
  year: 2018
  ident: D0NJ03386C-(cit5e)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC07434H
  contributor:
    fullname: Qiu
– volume: 83
  start-page: 14419
  year: 2018
  ident: D0NJ03386C-(cit8b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b02175
  contributor:
    fullname: Sun
– volume: 468
  start-page: 80
  year: 2019
  ident: D0NJ03386C-(cit9f)/*[position()=1]
  publication-title: Mol. Catal.
  doi: 10.1016/j.mcat.2019.02.019
  contributor:
    fullname: Yang
– volume: 6
  start-page: 1608
  year: 2019
  ident: D0NJ03386C-(cit7m)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00367C
  contributor:
    fullname: Wang
– volume: 21
  start-page: 3858
  year: 2019
  ident: D0NJ03386C-(cit7l)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C9GC01175G
  contributor:
    fullname: Xie
– volume: 31
  start-page: 67
  year: 2020
  ident: D0NJ03386C-(cit5d)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.05.041
  contributor:
    fullname: Wang
– volume: 55
  start-page: 8995
  year: 2019
  ident: D0NJ03386C-(cit7k)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC03789F
  contributor:
    fullname: Wu
– volume: 55
  start-page: 12615
  year: 2019
  ident: D0NJ03386C-(cit8c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC06924K
  contributor:
    fullname: Sun
– volume: 21
  start-page: 1112
  year: 2019
  ident: D0NJ03386C-(cit10d)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00023
  contributor:
    fullname: Xu
– volume: 55
  start-page: 2861
  year: 2019
  ident: D0NJ03386C-(cit12c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC10243K
  contributor:
    fullname: Sun
– volume: 44
  start-page: 8120
  year: 2020
  ident: D0NJ03386C-(cit12g)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/D0NJ00825G
  contributor:
    fullname: Lin
– volume: 360
  start-page: 1775
  year: 2018
  ident: D0NJ03386C-(cit7i)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201701630
  contributor:
    fullname: Zhao
– volume: 361
  start-page: 3712
  year: 2019
  ident: D0NJ03386C-(cit9a)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900544
  contributor:
    fullname: Liu
– volume: 84
  start-page: 8683
  year: 2019
  ident: D0NJ03386C-(cit4a)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.9b00451
  contributor:
    fullname: Ren
– volume: 360
  start-page: 4807
  year: 2018
  ident: D0NJ03386C-(cit12b)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201801122
  contributor:
    fullname: Li
– volume: 39
  start-page: 1975
  year: 1996
  ident: D0NJ03386C-(cit2a)/*[position()=1]
  publication-title: J. Med. Chem.
  doi: 10.1021/jm960008c
  contributor:
    fullname: Wang
– volume: 45
  start-page: 4310
  year: 2002
  ident: D0NJ03386C-(cit1a)/*[position()=1]
  publication-title: J. Med. Chem.
  doi: 10.1021/jm020878w
  contributor:
    fullname: Nussbaumer
– volume: 55
  start-page: 1013
  year: 2019
  ident: D0NJ03386C-(cit4c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC09250H
  contributor:
    fullname: Ye
– volume: 22
  start-page: 1593
  year: 1985
  ident: D0NJ03386C-(cit2b)/*[position()=1]
  publication-title: J. Heterocycl. Chem.
  doi: 10.1002/jhet.5570220625
  contributor:
    fullname: Nakazumi
– volume: 21
  start-page: 75
  year: 2019
  ident: D0NJ03386C-(cit1e)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b03508
  contributor:
    fullname: Sangeetha
– volume: 20
  start-page: 3144
  year: 2018
  ident: D0NJ03386C-(cit5b)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b01278
  contributor:
    fullname: Yang
– volume: 17
  start-page: 3507
  year: 2019
  ident: D0NJ03386C-(cit7n)/*[position()=1]
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C9OB00278B
  contributor:
    fullname: Wu
– volume: 361
  start-page: 4558
  year: 2019
  ident: D0NJ03386C-(cit4h)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900643
  contributor:
    fullname: Gan
– volume: 60
  start-page: 916
  year: 2019
  ident: D0NJ03386C-(cit7p)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2019.02.039
  contributor:
    fullname: Song
– volume: 362
  start-page: 2609
  year: 2020
  ident: D0NJ03386C-(cit8f)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.202000233
  contributor:
    fullname: Jiang
– volume: 361
  start-page: 2280
  year: 2019
  ident: D0NJ03386C-(cit7c)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900063
  contributor:
    fullname: Fu
– volume: 58
  start-page: 487
  year: 2017
  ident: D0NJ03386C-(cit8a)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2016.12.058
  contributor:
    fullname: Yang
– volume: 7
  start-page: 1884
  year: 2020
  ident: D0NJ03386C-(cit10c)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/D0QO00222D
  contributor:
    fullname: Yuan
– volume: 21
  start-page: 2890
  year: 2019
  ident: D0NJ03386C-(cit7o)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00907
  contributor:
    fullname: Rao
– volume: 7
  start-page: 14009
  year: 2019
  ident: D0NJ03386C-(cit4g)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.9b02511
  contributor:
    fullname: Li
– volume: 21
  start-page: 7938
  year: 2019
  ident: D0NJ03386C-(cit4i)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b02921
  contributor:
    fullname: Li
– volume: 35
  start-page: 1848
  year: 2015
  ident: D0NJ03386C-(cit7s)/*[position()=1]
  publication-title: Chin. J. Org. Chem.
  doi: 10.6023/cjoc201504039
  contributor:
    fullname: Hu
– volume: 20
  start-page: 6687
  year: 2018
  ident: D0NJ03386C-(cit7j)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b02733
  contributor:
    fullname: Sun
– volume: 6
  start-page: 1476
  year: 2019
  ident: D0NJ03386C-(cit4k)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00091G
  contributor:
    fullname: Zeng
– volume: 361
  start-page: 4483
  year: 2019
  ident: D0NJ03386C-(cit9b)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900691
  contributor:
    fullname: Sun
– volume: 24
  start-page: 853
  year: 1981
  ident: D0NJ03386C-(cit1d)/*[position()=1]
  publication-title: J. Med. Chem.
  doi: 10.1021/jm00139a017
  contributor:
    fullname: Holshouser
– volume: 31
  start-page: 667
  year: 2020
  ident: D0NJ03386C-(cit9e)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.07.053
  contributor:
    fullname: Song
– volume: 12
  start-page: 2397
  year: 2004
  ident: D0NJ03386C-(cit1b)/*[position()=1]
  publication-title: Bioorg. Med. Chem.
  doi: 10.1016/j.bmc.2004.02.002
  contributor:
    fullname: Kataoka
– volume: 55
  start-page: 5408
  year: 2019
  ident: D0NJ03386C-(cit9d)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC01047E
  contributor:
    fullname: Shang
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Snippet A set of transition-metal-free NaI/TBHP-mediated sulfonylation cyclization reactions of methylthiolated alkynones with sulfonyl hydrazides was developed, by...
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SubjectTerms Chemical reactions
Chemistry
Chemistry, Multidisciplinary
Crystallography
Functional groups
Hydrazides
Physical Sciences
Reagents
Science & Technology
Transition metals
Title Transition-metal-free sulfonylations of methylthiolated alkynones to synthesize 3-sulfonylated thioflavones
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