Metal-free sulfonyl radical-initiated cascade cyclization to access sulfonated indolo[1,2-]quinolines

A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP. Impressively, these products exhibit excellent fluorescence properties, which is promising for cell im...

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Published inChemical communications (Cambridge, England) Vol. 55; no. 84; pp. 12615 - 12618
Main Authors Sun, Kai, Chen, Xiao-Lan, Zhang, Yin-Li, Li, Kai, Huang, Xian-Qiang, Peng, Yu-Yu, Qu, Ling-Bo, Yu, Bing
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 17.10.2019
Royal Society of Chemistry
Subjects
Cascade chemical reactions
Chemistry
Chemistry, Multidisciplinary
Crystallography
cyclization reactions
Fluorescence
Hydrazides
image analysis
Indoles
Organic compounds
Physical Sciences
Quinoline
Science & Technology
QUINOLINE N-OXIDES
ONE-POT SYNTHESIS
ANNULATION
MEDIATED SULFONYLATION
STRATEGY
ALDEHYDES
QUINOXALIN-2(1H)-ONES
CATALYST
C-H ACTIVATION
EFFICIENT
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Abstract A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP. Impressively, these products exhibit excellent fluorescence properties, which is promising for cell imaging. A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP.
AbstractList A metal-free cascade reaction was developed for the synthesis of indolo[1,2-a]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP. Impressively, these products exhibit excellent fluorescence properties, which is promising for cell imaging.
A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP. Impressively, these products exhibit excellent fluorescence properties, which is promising for cell imaging. A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP.
A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and 1-(2-(arylethynyl)phenyl)indoles in the presence of TBAI/TBHP. Impressively, these products exhibit excellent fluorescence properties, which is promising for cell imaging.
Author Li, Kai
Peng, Yu-Yu
Chen, Xiao-Lan
Zhang, Yin-Li
Huang, Xian-Qiang
Qu, Ling-Bo
Sun, Kai
Yu, Bing
AuthorAffiliation Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation
School of Chemistry & Chemical Engineering
College of Chemistry
Changsha University of Science and Technology
Zhengzhou University
Liaocheng University
AuthorAffiliation_xml – name: Changsha University of Science and Technology
– name: Zhengzhou University
– name: Liaocheng University
– name: School of Chemistry & Chemical Engineering
– name: Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation
– name: College of Chemistry
Author_xml – sequence: 1
  givenname: Kai
  surname: Sun
  fullname: Sun, Kai
– sequence: 2
  givenname: Xiao-Lan
  surname: Chen
  fullname: Chen, Xiao-Lan
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  givenname: Yin-Li
  surname: Zhang
  fullname: Zhang, Yin-Li
– sequence: 4
  givenname: Kai
  surname: Li
  fullname: Li, Kai
– sequence: 5
  givenname: Xian-Qiang
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  surname: Peng
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  surname: Qu
  fullname: Qu, Ling-Bo
– sequence: 8
  givenname: Bing
  surname: Yu
  fullname: Yu, Bing
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Cites_doi 10.1002/slct.201900060
10.1002/adsc.201801122
10.1039/C7GC02330H
10.1021/acs.orglett.8b02627
10.1016/j.tetlet.2019.06.017
10.1021/acs.orglett.8b02733
10.1021/ol102342y
10.1039/C9GC01175G
10.1021/acssuschemeng.8b04339
10.1021/ol070475w
10.1021/jo501250u
10.1021/acs.orglett.9b00465
10.1039/C8QO00661J
10.1021/acs.orglett.5b01171
10.1016/j.tetlet.2018.12.016
10.1021/acs.joc.8b01343
10.1016/j.cclet.2019.03.034
10.1039/C7QO01048F
10.1039/C6SC05093J
10.1039/C8QO00882E
10.1039/C8QI00678D
10.1021/jo302112a
10.1039/C5CC04484G
10.1039/C6CC09471F
10.1021/acssuschemeng.9b00200
10.1016/j.tetlet.2016.12.058
10.1021/acssuschemeng.9b02822
10.1002/adsc.201801355
10.1002/chem.201705470
10.1021/acs.orglett.8b03768
10.1039/C8CC07434H
10.1039/C6CC02659A
10.1002/adsc.201900691
10.1021/acssuschemeng.8b05838
10.1515/pac-2018-0906
10.1021/acs.orglett.8b01238
10.1039/C9QO00091G
10.1039/C7CC09250D
10.1016/j.cclet.2019.04.008
10.1039/C9CC01047E
10.1002/adsc.201601407
10.1002/ajoc.201600205
10.1039/C9NJ02833A
10.1039/C8CC07398H
10.1039/C9OB01227C
10.1021/ja077444g
10.1039/C8CC04618B
10.1021/acssuschemeng.9b02511
10.1002/adsc.201900544
10.1021/acs.joc.8b01657
10.1016/j.tetlet.2019.02.039
10.1002/adsc.201701194
10.1002/adsc.201800989
10.1021/jo200638k
10.1002/ajoc.201700001
10.1007/s11426-018-9446-1
10.1021/acscatal.8b02194
10.1039/C8CC10243K
10.1002/anie.200804427
10.1016/j.tet.2019.07.014
10.1039/C8QO00679B
10.1016/j.cclet.2019.08.002
10.1039/C7GC02304A
10.1021/acs.joc.8b02175
10.1002/adsc.201900063
10.1021/acs.orglett.9b01175
10.1021/acssuschemeng.9b00497
10.1039/c8qo00679b
10.1039/c9ob01227c
10.1039/c5cc04484g
10.1039/c8qo00661j
10.1039/c7qo01048f
10.1039/c8cc10243k
10.1039/c9cc01047e
10.1039/c9qo00091g
10.1039/c6cc09471f
10.1039/c7gc02304a
10.1039/c8qi00678d
10.1039/c8qo00882e
10.1039/c9gc01175g
10.1039/c7cc09250d
10.1039/c8cc04618b
10.1039/c8nj06282j
10.1039/c8cc07398h
10.1039/c6sc05093j
10.1039/c8cc07434h
10.1039/c7gc02330h
10.1039/c6cc02659a
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Issue 84
Keywords QUINOLINE N-OXIDES
ONE-POT SYNTHESIS
ANNULATION
MEDIATED SULFONYLATION
STRATEGY
ALDEHYDES
QUINOXALIN-2(1H)-ONES
CATALYST
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1947659
10.1039/c9cc06924k
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Royal Society of Chemistry
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References Yang (C9CC06924K-(cit7d)/*[position()=1]) 2017; 359
Wei (C9CC06924K-(cit6c)/*[position()=1]) 2017; 19
Song (C9CC06924K-(cit6e)/*[position()=1]) 2019; 60
Muhammad (C9CC06924K-(cit6b)/*[position()=1]) 2019; 91
Verma (C9CC06924K-(cit3d)/*[position()=1]) 2011; 76
Li (C9CC06924K-(cit8d)/*[position()=1]) 2018; 360
Zhu (C9CC06924K-(cit10b)/*[position()=1]) 2018; 83
Liu (C9CC06924K-(cit2a)/*[position()=1]) 2018; 54
Hu (C9CC06924K-(cit9a)/*[position()=1]) 2018; 20
Peng (C9CC06924K-(cit1f)/*[position()=1]) 2019; 17
Li (C9CC06924K-(cit6g)/*[position()=1]) 2018; 8
Huang (C9CC06924K-(cit1j)/*[position()=1]) 2018; 20
Xie (C9CC06924K-(cit1m)/*[position()=1]) 2019; 7
Zhang (C9CC06924K-(cit6a)/*[position()=1]) 2019; 30
Miao (C9CC06924K-(cit1i)/*[position()=1]) 2019; 7
Li (C9CC06924K-(cit6f)/*[position()=1]) 2017; 8
Sun (C9CC06924K-(cit5f)/*[position()=1]) 2019; 75
Liu (C9CC06924K-(cit9c)/*[position()=1]) 2018; 83
Jing (C9CC06924K-(cit8g)/*[position()=1]) 2019; 21
Xie (C9CC06924K-(cit1e)/*[position()=1]) 2019; 62
Liu (C9CC06924K-(cit1h)/*[position()=1]) 2019; 43
Shukla (C9CC06924K-(cit3c)/*[position()=1]) 2012; 77
Xie (C9CC06924K-(cit4h)/*[position()=1]) 2019; 21
Peng (C9CC06924K-(cit5d)/*[position()=1]) 2019
Sun (C9CC06924K-(cit1a)/*[position()=1]) 2018; 20
Fu (C9CC06924K-(cit10c)/*[position()=1]) 2019; 361
Wang (C9CC06924K-(cit6h)/*[position()=1]) 2018; 5
Sun (C9CC06924K-(cit1c)/*[position()=1]) 2019
Bao (C9CC06924K-(cit5a)/*[position()=1]) 2019; 60
Wang (C9CC06924K-(cit6d)/*[position()=1]) 2019; 60
Yang (C9CC06924K-(cit4d)/*[position()=1]) 2017; 58
Liu (C9CC06924K-(cit8a)/*[position()=1]) 2019; 361
Xie (C9CC06924K-(cit4f)/*[position()=1]) 2018; 5
Yang (C9CC06924K-(cit1b)/*[position()=1]) 2018; 5
Shang (C9CC06924K-(cit8c)/*[position()=1]) 2019; 55
Ahmed (C9CC06924K-(cit2c)/*[position()=1]) 2008; 130
Panteleev (C9CC06924K-(cit3e)/*[position()=1]) 2010; 12
Li (C9CC06924K-(cit5e)/*[position()=1]) 2019; 7
Liu (C9CC06924K-(cit8b)/*[position()=1]) 2019; 21
Xia (C9CC06924K-(cit4a)/*[position()=1]) 2016; 5
Yang (C9CC06924K-(cit7c)/*[position()=1]) 2019; 361
Sun (C9CC06924K-(cit8f)/*[position()=1]) 2019; 55
Qiu (C9CC06924K-(cit4b)/*[position()=1]) 2018; 54
Xie (C9CC06924K-(cit4g)/*[position()=1]) 2018; 6
Sun (C9CC06924K-(cit10a)/*[position()=1]) 2018; 83
Huang (C9CC06924K-(cit7a)/*[position()=1]) 2018; 54
Zeng (C9CC06924K-(cit8e)/*[position()=1]) 2019; 6
Xu (C9CC06924K-(cit1n)/*[position()=1]) 2016; 52
Gao (C9CC06924K-(cit3b)/*[position()=1]) 2014; 79
Sun (C9CC06924K-(cit5b)/*[position()=1]) 2015; 51
Gao (C9CC06924K-(cit11a)/*[position()=1]) 2017; 53
Dong (C9CC06924K-(cit1l)/*[position()=1]) 2019; 4
Fu (C9CC06924K-(cit5c)/*[position()=1]) 2017; 6
Li (C9CC06924K-(cit1g)/*[position()=1]) 2019; 361
Wang (C9CC06924K-(cit9d)/*[position()=1]) 2019; 21
Hu (C9CC06924K-(cit9b)/*[position()=1]) 2018; 5
Zhu (C9CC06924K-(cit7e)/*[position()=1]) 2018; 360
Verma (C9CC06924K-(cit2b)/*[position()=1]) 2009; 48
Hofman (C9CC06924K-(cit4c)/*[position()=1]) 2018; 24
Yin (C9CC06924K-(cit11b)/*[position()=1]) 2018; 54
Hulcoop (C9CC06924K-(cit3f)/*[position()=1]) 2007; 9
Wang (C9CC06924K-(cit7b)/*[position()=1]) 2018; 5
Xie (C9CC06924K-(cit1d)/*[position()=1]) 2019; 7
Peng (C9CC06924K-(cit1k)/*[position()=1]) 2019; 30
Liu (C9CC06924K-(cit3a)/*[position()=1]) 2015; 17
Xie (C9CC06924K-(cit4e)/*[position()=1]) 2017; 19
Li, R (WOS:000465500000001) 2018; 360
Xia, YY (WOS:000380260800007) 2016; 5
Muhammad, MH (WOS:000454937000004) 2019; 91
Xie, LY (WOS:000482173100055) 2019; 7
Ahmed, E (WOS:000252634600003) 2008; 130
Shukla, SP (WOS:000311073000046) 2012; 77
Song, TT (WOS:000463127100007) 2019; 60
Shang, TY (WOS:000468369900001) 2019; 55
Xie, LY (WOS:000452344900110) 2018; 6
Xie, LY (WOS:000463462100080) 2019; 7
Hulcoop, DG (WOS:000245799200037) 2007; 9
Yang, GP (WOS:000448340900010) 2018; 5
Wang, LL (WOS:000474321900009) 2019; 60
Peng, LF (WOS:000482249800004) 2019; 30
Xie, LY (WOS:000443281400014) 2018; 5
Yang, WC (WOS:000405550800009) 2017; 359
Huang, XQ (WOS:000434367500041) 2018; 20
Xie, LY (WOS:000463714600010) 2019; 62
Sun, K (WOS:000449443100017) 2018; 20
Dong, DQ (WOS:000459929100037) 2019; 4
Li, GQ (WOS:000482173100040) 2019; 7
Peng, S (WOS:000506722300052) 2019; 30
Sun, K (WOS:000481008100001) 2019; 361
Huang, MH (WOS:000445458000001) 2018; 54
Gao, JL (WOS:000342719600009) 2014; 79
Li, HY (WOS:000397560500014) 2017; 8
Xu, H (WOS:000378234500021) 2016; 52
Sun, K (WOS:000357951400042) 2015; 51
Wang, JC (WOS:000461843900067) 2019; 21
Fu, WK (WOS:000401339200004) 2017; 6
Liu, Y (WOS:000471212100032) 2019; 21
Liu, Y (WOS:000447118100024) 2018; 83
Li, KJ (WOS:000461675600019) 2019; 361
Fu, R (WOS:000471326000009) 2019; 361
Hofman, K (WOS:000441691000006) 2018; 24
Hu, H (WOS:000447118200038) 2018; 20
Yang, WC (WOS:000467075800001) 2019; 361
Liu, XY (WOS:000356845000019) 2015; 17
Sun, K (WOS:000452929900018) 2018; 83
Miao, CX (WOS:000475838100011) 2019; 7
Zeng, FL (WOS:000466794900023) 2019; 6
Jing, CF (WOS:000456633000030) 2019; 21
Li, HY (WOS:000444364800052) 2018; 8
Gao, M (WOS:000393797900023) 2017; 53
Wang, BB (WOS:000428091500008) 2018; 5
Yang, FL (WOS:000393264100001) 2017; 58
Xie, LY (WOS:000475506200013) 2019; 21
Sun, M (WOS:000482244700003) 2019; 75
Verma, AK (WOS:000263082300022) 2009; 48
Yin, JL (WOS:000447980500026) 2018; 54
Verma, AK (WOS:000292480300016) 2011; 76
Xie, LY (WOS:000417758700014) 2017; 19
Liu, XC (WOS:000482071700007) 2019; 361
Wei, W (WOS:000417758700011) 2017; 19
Zhang, YL (WOS:000474501000002) 2019; 30
Qiu, GYS (WOS:000449274400002) 2018; 54
Liu, RX (WOS:000423784500016) 2018; 54
Sun, K (WOS:000460683700028) 2019; 55
Zhu, J (WOS:000424093900001) 2018; 360
Bao, PL (WOS:000456353000002) 2019; 60
Peng, Y (WOS:000475661500008) 2019; 17
Panteleev, J (WOS:000284080400003) 2010; 12
Hu, H (WOS:000448344700002) 2018; 5
Zhu, XT (WOS:000444364600026) 2018; 83
Zhou, Y (WOS:000459738600023) 2019; 43
Wang, XF (WOS:000443281400006) 2018; 5
References_xml – volume: 4
  start-page: 2480
  year: 2019
  ident: C9CC06924K-(cit1l)/*[position()=1]
  publication-title: ChemistrySelect
  doi: 10.1002/slct.201900060
– volume: 360
  start-page: 4807
  year: 2018
  ident: C9CC06924K-(cit8d)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201801122
– volume: 19
  start-page: 5608
  year: 2017
  ident: C9CC06924K-(cit6c)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C7GC02330H
– volume: 20
  start-page: 6157
  year: 2018
  ident: C9CC06924K-(cit9a)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b02627
– volume: 60
  start-page: 1845
  year: 2019
  ident: C9CC06924K-(cit6d)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2019.06.017
– volume: 20
  start-page: 6687
  year: 2018
  ident: C9CC06924K-(cit1a)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b02733
– volume: 12
  start-page: 5092
  year: 2010
  ident: C9CC06924K-(cit3e)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol102342y
– volume: 21
  start-page: 3858
  year: 2019
  ident: C9CC06924K-(cit4h)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C9GC01175G
– volume: 6
  start-page: 16976
  year: 2018
  ident: C9CC06924K-(cit4g)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.8b04339
– volume: 9
  start-page: 1761
  year: 2007
  ident: C9CC06924K-(cit3f)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol070475w
– volume: 79
  start-page: 9000
  year: 2014
  ident: C9CC06924K-(cit3b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo501250u
– volume: 21
  start-page: 1863
  year: 2019
  ident: C9CC06924K-(cit9d)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00465
– volume: 5
  start-page: 2604
  year: 2018
  ident: C9CC06924K-(cit4f)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C8QO00661J
– volume: 17
  start-page: 2936
  year: 2015
  ident: C9CC06924K-(cit3a)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b01171
– volume: 60
  start-page: 214
  year: 2019
  ident: C9CC06924K-(cit5a)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2018.12.016
– volume: 83
  start-page: 9890
  year: 2018
  ident: C9CC06924K-(cit10b)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b01343
– volume: 30
  start-page: 1361
  year: 2019
  ident: C9CC06924K-(cit6a)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.03.034
– volume: 5
  start-page: 958
  year: 2018
  ident: C9CC06924K-(cit6h)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C7QO01048F
– volume: 8
  start-page: 2610
  year: 2017
  ident: C9CC06924K-(cit6f)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C6SC05093J
– volume: 5
  start-page: 2925
  year: 2018
  ident: C9CC06924K-(cit9b)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C8QO00882E
– volume: 5
  start-page: 2472
  year: 2018
  ident: C9CC06924K-(cit1b)/*[position()=1]
  publication-title: Inorg. Chem. Front.
  doi: 10.1039/C8QI00678D
– volume: 77
  start-page: 10382
  year: 2012
  ident: C9CC06924K-(cit3c)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo302112a
– volume: 51
  start-page: 12111
  year: 2015
  ident: C9CC06924K-(cit5b)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C5CC04484G
– volume: 53
  start-page: 921
  year: 2017
  ident: C9CC06924K-(cit11a)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC09471F
– volume: 7
  start-page: 7193
  year: 2019
  ident: C9CC06924K-(cit1d)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.9b00200
– volume: 58
  start-page: 487
  year: 2017
  ident: C9CC06924K-(cit4d)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2016.12.058
– volume: 7
  start-page: 14153
  year: 2019
  ident: C9CC06924K-(cit1m)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.9b02822
– volume: 361
  start-page: 1700
  year: 2019
  ident: C9CC06924K-(cit7c)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201801355
– volume: 24
  start-page: 11852
  year: 2018
  ident: C9CC06924K-(cit4c)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201705470
– volume: 21
  start-page: 486
  year: 2019
  ident: C9CC06924K-(cit8g)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b03768
– volume: 54
  start-page: 12561
  year: 2018
  ident: C9CC06924K-(cit4b)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC07434H
– volume: 52
  start-page: 8002
  year: 2016
  ident: C9CC06924K-(cit1n)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC02659A
– year: 2019
  ident: C9CC06924K-(cit1c)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900691
– volume: 7
  start-page: 12008
  year: 2019
  ident: C9CC06924K-(cit1i)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.8b05838
– volume: 91
  start-page: 33
  year: 2019
  ident: C9CC06924K-(cit6b)/*[position()=1]
  publication-title: Pure Appl. Chem.
  doi: 10.1515/pac-2018-0906
– volume: 20
  start-page: 3332
  year: 2018
  ident: C9CC06924K-(cit1j)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.8b01238
– volume: 6
  start-page: 1476
  year: 2019
  ident: C9CC06924K-(cit8e)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00091G
– volume: 54
  start-page: 1225
  year: 2018
  ident: C9CC06924K-(cit2a)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C7CC09250D
– volume: 30
  start-page: 1481
  year: 2019
  ident: C9CC06924K-(cit1k)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.04.008
– volume: 55
  start-page: 5408
  year: 2019
  ident: C9CC06924K-(cit8c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC01047E
– volume: 359
  start-page: 2390
  year: 2017
  ident: C9CC06924K-(cit7d)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201601407
– volume: 5
  start-page: 878
  year: 2016
  ident: C9CC06924K-(cit4a)/*[position()=1]
  publication-title: Asian J. Org. Chem.
  doi: 10.1002/ajoc.201600205
– volume: 43
  start-page: 12221
  year: 2019
  ident: C9CC06924K-(cit1h)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/C9NJ02833A
– volume: 54
  start-page: 12093
  year: 2018
  ident: C9CC06924K-(cit11b)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC07398H
– volume: 17
  start-page: 6570
  year: 2019
  ident: C9CC06924K-(cit1f)/*[position()=1]
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/C9OB01227C
– volume: 130
  start-page: 1118
  year: 2008
  ident: C9CC06924K-(cit2c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja077444g
– volume: 54
  start-page: 10791
  year: 2018
  ident: C9CC06924K-(cit7a)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC04618B
– volume: 7
  start-page: 14009
  year: 2019
  ident: C9CC06924K-(cit5e)/*[position()=1]
  publication-title: ACS Sustainable Chem. Eng.
  doi: 10.1021/acssuschemeng.9b02511
– volume: 361
  start-page: 3712
  year: 2019
  ident: C9CC06924K-(cit8a)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900544
– volume: 83
  start-page: 11727
  year: 2018
  ident: C9CC06924K-(cit9c)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b01657
– volume: 60
  start-page: 916
  year: 2019
  ident: C9CC06924K-(cit6e)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2019.02.039
– volume: 360
  start-page: 386
  year: 2018
  ident: C9CC06924K-(cit7e)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201701194
– volume: 361
  start-page: 1033
  year: 2019
  ident: C9CC06924K-(cit1g)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201800989
– volume: 76
  start-page: 5670
  year: 2011
  ident: C9CC06924K-(cit3d)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo200638k
– volume: 6
  start-page: 492
  year: 2017
  ident: C9CC06924K-(cit5c)/*[position()=1]
  publication-title: Asian J. Org. Chem.
  doi: 10.1002/ajoc.201700001
– volume: 62
  start-page: 460
  year: 2019
  ident: C9CC06924K-(cit1e)/*[position()=1]
  publication-title: Sci. China: Chem.
  doi: 10.1007/s11426-018-9446-1
– volume: 8
  start-page: 8237
  year: 2018
  ident: C9CC06924K-(cit6g)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.8b02194
– volume: 55
  start-page: 2861
  year: 2019
  ident: C9CC06924K-(cit8f)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC10243K
– volume: 48
  start-page: 1138
  year: 2009
  ident: C9CC06924K-(cit2b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.200804427
– volume: 75
  start-page: 130456
  year: 2019
  ident: C9CC06924K-(cit5f)/*[position()=1]
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2019.07.014
– volume: 5
  start-page: 2555
  year: 2018
  ident: C9CC06924K-(cit7b)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C8QO00679B
– year: 2019
  ident: C9CC06924K-(cit5d)/*[position()=1]
  publication-title: Chin. Chem. Lett.
  doi: 10.1016/j.cclet.2019.08.002
– volume: 19
  start-page: 5642
  year: 2017
  ident: C9CC06924K-(cit4e)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C7GC02304A
– volume: 83
  start-page: 14419
  year: 2018
  ident: C9CC06924K-(cit10a)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b02175
– volume: 361
  start-page: 2280
  year: 2019
  ident: C9CC06924K-(cit10c)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201900063
– volume: 21
  start-page: 4019
  year: 2019
  ident: C9CC06924K-(cit8b)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b01175
– 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
– volume: 17
  start-page: 2936
  year: 2015
  ident: WOS:000356845000019
  article-title: Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.5b01171
– 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: 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
– 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: 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
– volume: 7
  start-page: 7193
  year: 2019
  ident: WOS:000463462100080
  article-title: Clean Preparation of Quinolin-2-yl Substituted Ureas in Water
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b00200
– volume: 7
  start-page: 12008
  year: 2019
  ident: WOS:000475838100011
  article-title: Long-Chained Acidic Ionic Liquids-Catalyzed Cyclization of 2-Substituted Aminoaromatics with beta-Diketones: A Metal-Free Strategy to Construct Benzoazoles
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b00497
– volume: 6
  start-page: 16976
  year: 2018
  ident: WOS:000452344900110
  article-title: Waste-Minimized Protocol for the Synthesis of Sulfonylated N-Heteroaromatics in Water
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.8b04339
– volume: 83
  start-page: 11727
  year: 2018
  ident: WOS:000447118100024
  article-title: Phosphorus Radical-Initiated Cascade Reaction To Access 2-Phosphoryl-Substituted Quinoxalines
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.8b01657
– volume: 48
  start-page: 1138
  year: 2009
  ident: WOS:000263082300022
  article-title: A Copper-Catalyzed Tandem Synthesis of Indolo- and Pyrrolo[2,1-a]isoquinolines
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200804427
– 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
– volume: 5
  start-page: 2555
  year: 2018
  ident: WOS:000443281400006
  article-title: Synthesis of 6-(sulfonylmethyl)phenanthridines through a reaction of aryldiazonium tetrafluoroborates, sulfur dioxide, and vinyl azides
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c8qo00679b
– volume: 17
  start-page: 6570
  year: 2019
  ident: WOS:000475661500008
  article-title: Exploring the ring-opening reactions of imidazo[1,5-a]quinolines for the synthesis of imides under photochemical conditions
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c9ob01227c
– volume: 51
  start-page: 12111
  year: 2015
  ident: WOS:000357951400042
  article-title: H-phosphonate-mediated sulfonylation of heteroaromatic N-oxides: a mild and metal-free one-pot synthesis of 2-sulfonyl quinolines/pyridines
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c5cc04484g
– volume: 5
  start-page: 2604
  year: 2018
  ident: WOS:000443281400014
  article-title: Metal-free deoxygenative sulfonylation of quinoline N-oxides with sodium sulfinates via a dual radical coupling process
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c8qo00661j
– volume: 79
  start-page: 9000
  year: 2014
  ident: WOS:000342719600009
  article-title: One-Pot Approach to 1,2-Disubstituted Indoles via Cu(II)-Catalyzed Coupling/Cyclization under Aerobic Conditions and Its Application for the Synthesis of Polycyclic Indoles
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo501250u
– 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: 5
  start-page: 958
  year: 2018
  ident: WOS:000428091500008
  article-title: Radical rearrangement of N-sulfonyl-N-aryl propynamides: proceeding with homolytic N-SO2 bond cleavage and 6-endo-dig cyclization toward 3-sulfonyl-2(1H)-quinolinones
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c7qo01048f
– 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
– 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
– 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
– volume: 6
  start-page: 492
  year: 2017
  ident: WOS:000401339200004
  article-title: Iodine-Mediated Sulfonylation of Quinoline N-Oxides: a Mild and Metal-Free One-Pot Synthesis of 2-Sulfonyl Quinolines
  publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ajoc.201700001
– 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
– 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: 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
– volume: 53
  start-page: 921
  year: 2017
  ident: WOS:000393797900023
  article-title: An easily accessible aggregation-induced emission probe for lipid droplet-specific imaging and movement tracking
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc09471f
– 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
– 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
– volume: 77
  start-page: 10382
  year: 2012
  ident: WOS:000311073000046
  article-title: Palladium-Catalyzed Sonogashira-Coupling Conjoined C-H Activation: A Regioselective Tandem Strategy to Access Indolo- and Pyrrolo[1,2-a]quinolines
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo302112a
– volume: 20
  start-page: 6157
  year: 2018
  ident: WOS:000447118200038
  article-title: Silver-Catalyzed Radical Cascade Cyclization toward 1,5-/1,3-Dicarbonyl Heterocycles: An Atom-/Step-Economical Strategy Leading to Chromenopyridines and Isoxazole-/Pyrazole-Containing Chroman-4-Ones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b02627
– volume: 361
  start-page: 1033
  year: 2019
  ident: WOS:000461675600019
  article-title: Electrochemical Dehydrogenative Cross-Coupling of Quinoxalin-2(1H)-ones with Amines for the Synthesis of 3-Aminoquinoxalinones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201800989
– volume: 5
  start-page: 2472
  year: 2018
  ident: WOS:000448340900010
  article-title: Ce(III)-Containing tungstotellurate(VI) with a sandwich structure: an efficient Lewis acid-base catalyst for the condensation cyclization of 1,3-diketones with hydrazines/hydrazides or diamines
  publication-title: INORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c8qi00678d
– volume: 60
  start-page: 1845
  year: 2019
  ident: WOS:000474321900009
  article-title: Metal-free I2O5-mediated oxidative synthesis of sulfonylated benzofurans through cyclization reaction of 1,6-enynes and arylsulfonylhydrazides
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2019.06.017
– 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
– volume: 130
  start-page: 1118
  year: 2008
  ident: WOS:000252634600003
  article-title: High mobility single-crystal field-effect transistors from bisindoloquinoline semiconductors
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja077444g
– 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: 12
  start-page: 5092
  year: 2010
  ident: WOS:000284080400003
  article-title: C-H Bond Functionalization in the Synthesis of Fused 1,2,3-Triazoles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol102342y
– volume: 5
  start-page: 2925
  year: 2018
  ident: WOS:000448344700002
  article-title: Silver-catalyzed decarboxylative cascade radical cyclization of tert-carboxylic acids and o-(allyloxy)arylaldehydes towards chroman-4-one derivatives
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c8qo00882e
– 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
– volume: 54
  start-page: 1225
  year: 2018
  ident: WOS:000423784500016
  article-title: Synthesis of indolizine derivatives containing eight-membered rings via a gold-catalyzed two-fold hydroarylation of diynes
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c7cc09250d
– volume: 54
  start-page: 10791
  year: 2018
  ident: WOS:000445458000001
  article-title: Recent advances in radical transformations of internal alkynes
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc04618b
– 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: 76
  start-page: 5670
  year: 2011
  ident: WOS:000292480300016
  article-title: Synthesis of 5-Iodopyrrolo[1,2-a]quinolines and Indolo[1,2-a]quinolines via Iodine-Mediated Electrophilic and Regioselective 6-endo-dig Ring Closure
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo200638k
– 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
– volume: 4
  start-page: 2480
  year: 2019
  ident: WOS:000459929100037
  article-title: Merrifield Resin Supported Ionic Liquids/Iodide as an Efficient and Recyclable Catalyst for the Synthesis of Benzimidazoles
  publication-title: CHEMISTRYSELECT
  doi: 10.1002/slct.201900060
– volume: 361
  start-page: 1700
  year: 2019
  ident: WOS:000467075800001
  article-title: Aliphatic Aldehydes: Novel Radical Alkylating Reagents
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201801355
– volume: 54
  start-page: 12093
  year: 2018
  ident: WOS:000447980500026
  article-title: Rational design of a lipid-droplet-polarity based fluorescent probe for potential cancer diagnosis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc07398h
– 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
– volume: 21
  start-page: 486
  year: 2019
  ident: WOS:000456633000030
  article-title: Copper-Catalyzed C4-H Regioselective Phosphorylation/Trifluoromethylation of Free 1-Naphthylamines
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b03768
– volume: 24
  start-page: 11852
  year: 2018
  ident: WOS:000441691000006
  article-title: Radicals and Sulfur Dioxide: A Versatile Combination for the Construction of Sulfonyl-Containing Molecules
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201705470
– volume: 91
  start-page: 33
  year: 2019
  ident: WOS:000454937000004
  article-title: Applications of H-phosphonates for C element bond formation
  publication-title: PURE AND APPLIED CHEMISTRY
  doi: 10.1515/pac-2018-0906
– 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
– 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
– volume: 7
  start-page: 14153
  year: 2019
  ident: WOS:000482173100055
  article-title: Visible-Light-Initiated Decarboxylative Alkylation of Quinoxalin-2(1H)-ones with Phenyliodine(III) Dicarboxylates in Recyclable Ruthenium(II) Catalytic System
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b02822
– 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
– volume: 62
  start-page: 460
  year: 2019
  ident: WOS:000463714600010
  article-title: Metal-free C3-alkoxycarbonylation of quinoxalin-2(1H)-ones with carbazates as ecofriendly ester sources
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-018-9446-1
– volume: 9
  start-page: 1761
  year: 2007
  ident: WOS:000245799200037
  article-title: Palladium-catalyzed annulation of aryl heterocycles with strained alkenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol070475w
– 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
– 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: 19
  start-page: 5608
  year: 2017
  ident: WOS:000417758700011
  article-title: Visible-light-enabled spirocyclization of alkynes leading to 3-sulfonyl and 3-sulfenyl azaspiro[4,5] trienones
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c7gc02330h
– 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
– volume: 5
  start-page: 878
  year: 2016
  ident: WOS:000380260800007
  article-title: Synthesis of -Ketosulfones by using Sulfonyl Chloride as a Sulfur Source
  publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ajoc.201600205
– volume: 52
  start-page: 8002
  year: 2016
  ident: WOS:000378234500021
  article-title: Insights into the unexpected chemoselectivity in Bronsted acid catalyzed cyclization of isatins with enaminones: convenient synthesis of pyrrolo[3,4-c]quinolin-1-ones and spirooxindoles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc02659a
– volume: 359
  start-page: 2390
  year: 2017
  ident: WOS:000405550800009
  article-title: Aldehydes as Carbon Radical Acceptors: Silver Nitrate Catalyzed Cascade Decarboxylation and Oxidative Cyclization toward Dihydroflavonoid Derivatives
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201601407
– volume: 83
  start-page: 9890
  year: 2018
  ident: WOS:000444364600026
  article-title: Substrate-Controlled Generation of 3-Sulfonylated 1-Indenones and 3-Arylated (Z)-Indenes via Cu-Catalyzed Radical Cyclization Cascades of o-Alkynylbenzonitriles
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.8b01343
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Snippet A metal-free cascade reaction was developed for the synthesis of indolo[1,2- a ]quinoline derivatives from arylsulfonyl hydrazides and...
A metal-free cascade reaction was developed for the synthesis of indolo[1,2-a]quinoline derivatives from arylsulfonyl hydrazides and...
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SubjectTerms Cascade chemical reactions
Chemistry
Chemistry, Multidisciplinary
Crystallography
cyclization reactions
Fluorescence
Hydrazides
image analysis
Indoles
Organic compounds
Physical Sciences
Quinoline
Science & Technology
Title Metal-free sulfonyl radical-initiated cascade cyclization to access sulfonated indolo[1,2-]quinolines
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