Metal-Free Photosynthesis of Alkylated Benzimidazo[2,1‑a]isoquinoline-6(5H)‑ones and Indolo[2,1‑a]isoquinolin-6(5H)‑ones in PEG-200

A visible-light-induced decarboxylation reaction was developed for the synthesis of alkylated benzimidazo­[2,1-a]­isoquinoline-6­(5H)-ones and indolo­[2,1-a]­isoquinolin-6­(5H)-ones under metal-free conditions. Impressively, metal catalysts and traditionally volatile organic solvents could be effect...

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Published inJournal of organic chemistry Vol. 86; no. 13; pp. 9055 - 9066
Main Authors Li, Hao-Cong, Sun, Kai, Li, Xiang, Wang, Si-Yang, Chen, Xiao-Lan, He, Shuai-Qi, Qu, Ling-Bo, Yu, Bing
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 02.07.2021
Amer Chemical Soc
Subjects
Chemistry
Chemistry, Organic
decarboxylation
organic chemistry
photosynthesis
Physical Sciences
Science & Technology
volatile organic compounds
ACIDS
PROGRESS
REDOX-ACTIVE ESTERS
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Abstract A visible-light-induced decarboxylation reaction was developed for the synthesis of alkylated benzimidazo­[2,1-a]­isoquinoline-6­(5H)-ones and indolo­[2,1-a]­isoquinolin-6­(5H)-ones under metal-free conditions. Impressively, metal catalysts and traditionally volatile organic solvents could be effectively avoided.
AbstractList A visible-light-induced decarboxylation reaction was developed for the synthesis of alkylated benzimidazo­[2,1-a]­isoquinoline-6­(5H)-ones and indolo­[2,1-a]­isoquinolin-6­(5H)-ones under metal-free conditions. Impressively, metal catalysts and traditionally volatile organic solvents could be effectively avoided.
A visible-light-induced decarboxylation reaction was developed for the synthesis of alkylated benzimidazo[2,1-a]isoquinoline-6(5H)-ones and indolo[2,1-a]isoquinolin-6(5H)-ones under metal-free conditions. Impressively, metal catalysts and traditionally volatile organic solvents could be effectively avoided.
Author Li, Hao-Cong
Chen, Xiao-Lan
Qu, Ling-Bo
Wang, Si-Yang
Sun, Kai
He, Shuai-Qi
Yu, Bing
Li, Xiang
AuthorAffiliation Green Catalysis Center, College of Chemistry
AuthorAffiliation_xml – name: Green Catalysis Center, College of Chemistry
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  givenname: Xiang
  surname: Li
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  orcidid: 0000-0002-3061-8456
  surname: Chen
  fullname: Chen, Xiao-Lan
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  orcidid: 0000-0002-2423-1212
  surname: Yu
  fullname: Yu, Bing
  email: bingyu@zzu.edu.cn
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Cites_doi 10.1021/acs.orglett.0c03548
10.6023/cjoc201909030
10.1002/ejoc.202000525
10.1002/anie.201902792
10.1002/anie.201901935
10.1039/c9cc09654j
10.1021/jacs.6b00250
10.1039/d0cc05946c
10.1002/adsc.201801355
10.1002/adsc.201901016
10.1039/d0gc03447a
10.1021/jacs.0c11138
10.1016/j.cclet.2019.07.015
10.1039/c9ob01979k
10.1021/cr100264t
10.1007/s11426-020-9811-6
10.1039/c8cc10243k
10.1039/c9gc01357a
10.1021/acs.joc.0c02107
10.1021/acs.orglett.1c00546
10.1038/nature14885
10.1039/d0qo01410a
10.1055/s-0036-1590935
10.1021/acs.orglett.9b02921
10.1021/acs.chemrev.0c00030
10.1002/cssc.201902817
10.1021/acs.orglett.9b02105
10.1002/adsc.202000214
10.1021/acscatal.0c01324
10.1021/acs.joc.9b03505
10.1007/s11426-019-9701-5
10.6023/cjoc202006068
10.1039/c9cc08348k
10.1039/d0qo01058h
10.1016/j.cclet.2021.01.021
10.1016/j.ejmech.2010.05.025
10.6023/cjoc202100016
10.1002/adsc.202000040
10.1021/acssuschemeng.8b04652
10.1016/j.cclet.2020.07.035
10.1039/d0qo00460j
10.1002/adsc.201701615
10.1039/c9cc07494e
10.1039/c8cc04618b
10.1002/anie.201915837
10.1039/c9qo01428d
10.1021/acs.joc.0c02500
10.1039/d0ob00877j
10.1039/d0cc02335c
10.1039/c9qo01334b
10.1039/c9cc02388g
10.1021/acscatal.0c04756
10.1039/d1ob00319d
10.1071/ch01114
10.1016/j.cclet.2021.02.057
10.1002/anie.201801277
10.1007/s11426-018-9399-2
10.1021/acs.chemrev.0c00278
10.1039/d0ob02383c
10.1039/c9cc01047e
10.1039/d0cc05391k
10.6023/cjoc201900002
10.1128/mcb.00035-15
10.1016/j.ejmech.2014.11.053
10.1021/acs.orglett.8b02670
10.1021/acs.joc.0c01688
10.1128/MCB.00035-15
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References ref1/cit1i
ref1/cit1h
ref1/cit1e
ref1/cit1d
ref1/cit1g
ref1/cit1f
ref2/cit2e
ref2/cit2d
ref13/cit13a
ref13/cit13b
ref12/cit12b
ref12/cit12a
ref2/cit2c
ref2/cit2b
ref2/cit2a
ref1/cit1a
ref1/cit1c
ref1/cit1b
ref5/cit5b
ref5/cit5c
ref5/cit5a
ref7/cit7d
ref3/cit3b
ref3/cit3c
ref3/cit3a
ref3/cit3f
ref3/cit3d
ref3/cit3e
ref7/cit7c
ref7/cit7b
ref7/cit7a
ref5/cit5h
ref5/cit5i
ref5/cit5f
ref5/cit5g
ref5/cit5d
ref5/cit5e
ref9/cit9c
ref9/cit9b
ref9/cit9a
ref11/cit11
ref8/cit8a
ref10/cit10a
ref8/cit8c
ref10/cit10b
ref8/cit8b
ref8/cit8e
ref8/cit8d
ref8/cit8g
ref8/cit8f
ref14/cit14
ref6/cit6d
ref4/cit4a
ref6/cit6e
ref4/cit4b
ref6/cit6f
ref4/cit4c
ref15/cit15
ref4/cit4d
ref4/cit4e
ref6/cit6a
ref4/cit4f
ref6/cit6b
ref4/cit4g
ref6/cit6c
ref4/cit4h
Zhou, MD (WOS:000531082100005) 2020; 40
Liu, XC (WOS:000502174900001) 2020; 13
Teng, F. (000670661000044.36) 2021; 1907
Jiang, J (WOS:000647702900007) 2021; 32
Shang, TY (WOS:000468369900001) 2019; 55
Yadav, G (WOS:000356734600036) 2015; 97
Sun, X (WOS:000531348400001) 2020; 362
Jiang, SS (WOS:000544474600019) 2020; 18
Liu, JG (WOS:000536953100038) 2020; 59
Li, Y (WOS:000542898200001) 2020; 56
Chen, Y (WOS:000456087200007) 2019; 62
Ouyang, XH (WOS:000449443100011) 2018; 20
Wang, Z (WOS:000518129500030) 2019; 39
Niu, PF (WOS:000557397600001) 2020; 2020
Hua, TB (WOS:000510956700002) 2020; 31
Zhang, HH (WOS:000524185600001) 2020; 63
Dong, JY (WOS:000583607100033) 2020; 56
Bao, PL (WOS:000511876900006) 2020; 7
Jin, J (WOS:000360594100030) 2015; 525
Fu, LQ (WOS:000607016900022) 2020; 22
Chou, YC (WOS:000357457900014) 2015; 35
Jia, JQ (WOS:000511876900021) 2020; 7
Huang, MH (WOS:000445458000001) 2018; 54
Sun, K (WOS:000531612200003) 2020; 362
Lei, L (WOS:000634379700001) 2021; 19
Song, RJ (WOS:000474806700001) 2019; 58
Zhao, QQ (WOS:000634840300045) 2021; 41
Liu, Y (WOS:000612557200048) 2021; 143
Lyu, XL (WOS:000476957200074) 2019; 21
Liu, L (WOS:000574920600028) 2020; 85
Wei, W (WOS:000452344900140) 2018; 6
Boora, R (WOS:000498709600009) 2019; 17
Cornella, J (WOS:000371103900026) 2016; 138
Li, YJ (WOS:000418282000001) 2017; 49
Yu, XY (WOS:000611061700015) 2021; 121
Wang, X (WOS:000501150200016) 2019; 55
Wanka, L (WOS:000318892600017) 2013; 113
Yang, WC (WOS:000467075800001) 2019; 361
Wei, YL (WOS:000468478100016) 2019; 55
Deady, LW (WOS:000173622300008) 2001; 54
Parida, SK (WOS:000618540300051) 2021; 11
Niu, KK (WOS:000574031500024) 2020; 56
Moriarty, E (WOS:000281568600029) 2010; 45
Crespi, S (WOS:000571431700012) 2020; 120
Li, GQ (WOS:000489200100053) 2019; 21
Gao, F (WOS:000592978100044) 2020; 85
Yuan, XY (WOS:000598969200007) 2020; 40
Guo, YQ (WOS:000631439700074) 2021; 23
Pramanik, MMD (WOS:000562454200020) 2020; 7
Sun, K (WOS:000608623000007) 2021; 23
Zeng, FL (WOS:000497150900013) 2019; 361
Pitzer, L (WOS:000476608700051) 2019; 58
Gan, ZY (WOS:000557107400003) 2020; 63
Zeng, FL (WOS:000620718900014) 2021; 8
Taublaender, MJ (WOS:000444225100005) 2018; 57
Sun, K (WOS:000616326200002) 2021; 8
Xiao, W (WOS:000600917100014) 2020; 31
Ye, C (WOS:000606840200083) 2021; 86
Sun, K (WOS:000460683700028) 2019; 55
Yu, Q (WOS:000471798100019) 2019; 21
Correia, JTM (WOS:000506632200001) 2020; 56
Murarka, S (WOS:000431487200001) 2018; 360
Meng, N (WOS:000538764000007) 2020; 85
Pan, CD (WOS:000612478400014) 2021; 19
Yuan, Y (WOS:000543663800008) 2020; 10
Wang, YT (WOS:000519582800024) 2020; 56
References_xml – ident: ref1/cit1i
  doi: 10.1021/acs.orglett.0c03548
– ident: ref8/cit8b
  doi: 10.6023/cjoc201909030
– ident: ref8/cit8d
  doi: 10.1002/ejoc.202000525
– ident: ref8/cit8e
  doi: 10.1002/anie.201902792
– ident: ref10/cit10a
  doi: 10.1002/anie.201901935
– ident: ref8/cit8a
  doi: 10.1039/c9cc09654j
– ident: ref15/cit15
  doi: 10.1021/jacs.6b00250
– ident: ref3/cit3e
  doi: 10.1039/d0cc05946c
– ident: ref6/cit6e
  doi: 10.1002/adsc.201801355
– ident: ref4/cit4d
  doi: 10.1002/adsc.201901016
– ident: ref5/cit5b
  doi: 10.1039/d0gc03447a
– ident: ref9/cit9b
  doi: 10.1021/jacs.0c11138
– ident: ref1/cit1f
  doi: 10.1016/j.cclet.2019.07.015
– ident: ref4/cit4e
  doi: 10.1039/c9ob01979k
– ident: ref11/cit11
  doi: 10.1021/cr100264t
– ident: ref5/cit5c
  doi: 10.1007/s11426-020-9811-6
– ident: ref4/cit4a
  doi: 10.1039/c8cc10243k
– ident: ref1/cit1d
  doi: 10.1039/c9gc01357a
– ident: ref10/cit10b
  doi: 10.1021/acs.joc.0c02107
– ident: ref3/cit3d
  doi: 10.1021/acs.orglett.1c00546
– ident: ref3/cit3a
  doi: 10.1038/nature14885
– ident: ref9/cit9c
  doi: 10.1039/d0qo01410a
– ident: ref6/cit6f
  doi: 10.1055/s-0036-1590935
– ident: ref13/cit13b
  doi: 10.1021/acs.orglett.9b02921
– ident: ref5/cit5g
  doi: 10.1021/acs.chemrev.0c00030
– ident: ref9/cit9a
  doi: 10.1002/cssc.201902817
– ident: ref7/cit7d
  doi: 10.1021/acs.orglett.9b02105
– ident: ref12/cit12b
  doi: 10.1002/adsc.202000214
– ident: ref4/cit4b
  doi: 10.1021/acscatal.0c01324
– ident: ref13/cit13a
  doi: 10.1021/acs.joc.9b03505
– ident: ref5/cit5a
  doi: 10.1007/s11426-019-9701-5
– ident: ref6/cit6c
  doi: 10.6023/cjoc202006068
– ident: ref6/cit6b
  doi: 10.1039/c9cc08348k
– ident: ref1/cit1b
  doi: 10.1039/d0qo01058h
– ident: ref5/cit5h
  doi: 10.1016/j.cclet.2021.01.021
– ident: ref2/cit2d
  doi: 10.1016/j.ejmech.2010.05.025
– ident: ref3/cit3b
  doi: 10.6023/cjoc202100016
– ident: ref4/cit4c
  doi: 10.1002/adsc.202000040
– ident: ref3/cit3f
  doi: 10.1021/acssuschemeng.8b04652
– ident: ref6/cit6d
  doi: 10.1016/j.cclet.2020.07.035
– ident: ref5/cit5e
  doi: 10.1039/d0qo00460j
– ident: ref7/cit7c
  doi: 10.1002/adsc.201701615
– ident: ref8/cit8g
  doi: 10.1039/c9cc07494e
– ident: ref3/cit3c
  doi: 10.1039/c8cc04618b
– ident: ref1/cit1a
  doi: 10.1002/anie.201915837
– ident: ref8/cit8c
  doi: 10.1039/c9qo01428d
– ident: ref5/cit5i
  doi: 10.1021/acs.joc.0c02500
– ident: ref4/cit4g
  doi: 10.1039/d0ob00877j
– ident: ref1/cit1c
  doi: 10.1039/d0cc02335c
– ident: ref12/cit12a
  doi: 10.1039/c9qo01334b
– ident: ref4/cit4h
  doi: 10.1039/c9cc02388g
– ident: ref7/cit7a
  doi: 10.1021/acscatal.0c04756
– ident: ref1/cit1h
  doi: 10.1039/d1ob00319d
– ident: ref2/cit2c
  doi: 10.1071/ch01114
– ident: ref1/cit1e
  doi: 10.1016/j.cclet.2021.02.057
– ident: ref2/cit2a
  doi: 10.1002/anie.201801277
– ident: ref5/cit5d
  doi: 10.1007/s11426-018-9399-2
– ident: ref6/cit6a
  doi: 10.1021/acs.chemrev.0c00278
– ident: ref4/cit4f
  doi: 10.1039/d0ob02383c
– ident: ref5/cit5f
  doi: 10.1039/c9cc01047e
– ident: ref7/cit7b
  doi: 10.1039/d0cc05391k
– ident: ref1/cit1g
  doi: 10.6023/cjoc201900002
– ident: ref2/cit2b
  doi: 10.1128/mcb.00035-15
– ident: ref2/cit2e
  doi: 10.1016/j.ejmech.2014.11.053
– ident: ref8/cit8f
  doi: 10.1021/acs.orglett.8b02670
– ident: ref14/cit14
  doi: 10.1021/acs.joc.0c01688
– volume: 56
  start-page: 6907
  year: 2020
  ident: WOS:000542898200001
  article-title: Radical-mediated oxidative annulations of 1,n-enynes involving C-H functionalization
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/d0cc02335c
– volume: 525
  start-page: 87
  year: 2015
  ident: WOS:000360594100030
  article-title: Alcohols as alkylating agents in heteroarene C-H functionalization
  publication-title: NATURE
  doi: 10.1038/nature14885
– volume: 40
  start-page: 598
  year: 2020
  ident: WOS:000531082100005
  article-title: Progress in Photoinduced Decarboxylative Radical Cross-Coupling of Alkyl Carboxylic Acids and Their Derivatives
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201909030
– volume: 18
  start-page: 4843
  year: 2020
  ident: WOS:000544474600019
  article-title: Manganese(iii)-promoted tandem phosphinoylation/cyclization of 2-arylindoles/2-arylbenzimidazoles with disubstituted phosphine oxides
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/d0ob00877j
– volume: 120
  start-page: 9790
  year: 2020
  ident: WOS:000571431700012
  article-title: Generation of Alkyl Radicals: From the Tyranny of Tin to the Photon Democracy
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00278
– volume: 31
  start-page: 311
  year: 2020
  ident: WOS:000510956700002
  article-title: Recent advances in asymmetric synthesis of 2-substituted indoline derivatives
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.07.015
– volume: 121
  start-page: 506
  year: 2021
  ident: WOS:000611061700015
  article-title: Visible Light-Driven Radical-Mediated C-C Bond Cleavage/Functionalization in Organic Synthesis
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.0c00030
– volume: 22
  start-page: 9518
  year: 2020
  ident: WOS:000607016900022
  article-title: The Domino Chromone Annulation and a Transient Halogenation-Mediated C-H Alkenylation toward 3-Vinyl Chromones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.0c03548
– volume: 85
  start-page: 11892
  year: 2020
  ident: WOS:000574920600028
  article-title: Redox-Neutral Photocatalytic Radical Cascade Cyclization for the Synthesis of CH2CN/CF2COOEt/CF3-Containing Benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-One Derivatives
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.0c01688
– volume: 7
  start-page: 492
  year: 2020
  ident: WOS:000511876900006
  article-title: Visible-light-promoted acridine red catalyzed aerobic oxidative decarboxylative acylation of alpha-oxo-carboxylic acids with quinoxalin-2(1H)-ones
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo01334b
– volume: 20
  start-page: 6659
  year: 2018
  ident: WOS:000449443100011
  article-title: Alkylamination of Styrenes with Alkyl N-Hydroxyphthalimide Esters and Amines by B(C6H5)(3)-Facilitated Photoredox Catalysis
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.8b02670
– volume: 362
  start-page: 2701
  year: 2020
  ident: WOS:000531348400001
  article-title: Visible-Light-Promoted Regio- and Stereoselective Oxyalkenyl-Ation of Phosphinyl Allenes
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.202000214
– volume: 63
  start-page: 1652
  year: 2020
  ident: WOS:000557107400003
  article-title: Visible-light-induced regioselective cross-dehydrogenative coupling of 2-isothiocyanatonaphthalenes with amines using molecular oxygen
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-020-9811-6
– volume: 1907
  year: 2021
  ident: 000670661000044.36
  article-title: Visible-light-initiated tandem synthesis of difluoromethylated oxindoles in 2- MeTHF under additive-, metal catalyst-, external photosensitizer-free and mild conditions
  publication-title: Chin. Chem. Lett.
– volume: 21
  start-page: 7938
  year: 2019
  ident: WOS:000489200100053
  article-title: Photocatalyst-Free Visible-Light-Promoted C(sp(2))-S Coupling: A Strategy for the Preparation of S-Aryl Dithiocarbamates
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b02921
– volume: 55
  start-page: 5922
  year: 2019
  ident: WOS:000468478100016
  article-title: Synthesis of indolo[2,1-a]isoquinoline derivatives via visible-light-induced radical cascade cyclization reactions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc02388g
– volume: 62
  start-page: 24
  year: 2019
  ident: WOS:000456087200007
  article-title: Visible light-driven organic photochemical synthesis in China
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-018-9399-2
– volume: 32
  start-page: 1637
  year: 2021
  ident: WOS:000647702900007
  article-title: The application of clean production in organic synthesis
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2021.02.057
– volume: 360
  start-page: 1735
  year: 2018
  ident: WOS:000431487200001
  article-title: N-(Acyloxy)phthalimides as Redox-Active Esters in Cross-Coupling Reactions
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201701615
– 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
– 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: 2020
  start-page: 5801
  year: 2020
  ident: WOS:000557397600001
  article-title: One-Electron Reduction of Redox-Active Esters to Generate Carbon-Centered Radicals
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.202000525
– 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: 54
  start-page: 529
  year: 2001
  ident: WOS:000173622300008
  article-title: Reduced benzimidazo[2,1-a] isoquinolines. Synthesis and cytotoxicity studies
  publication-title: AUSTRALIAN JOURNAL OF CHEMISTRY
– volume: 56
  start-page: 12652
  year: 2020
  ident: WOS:000583607100033
  article-title: Visible-light-mediated photoredox minisci C-H alkylation with alkyl boronic acids using molecular oxygen as an oxidant
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/d0cc05946c
– volume: 39
  start-page: 3594
  year: 2019
  ident: WOS:000518129500030
  article-title: Radical Cyclization Strategy towards Indolo[1,2-a]quinolines
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201900002
– volume: 7
  start-page: 602
  year: 2020
  ident: WOS:000511876900021
  article-title: Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo01428d
– volume: 59
  start-page: 8195
  year: 2020
  ident: WOS:000536953100038
  article-title: Polarity Umpolung Strategy for the Radical Alkylation of Alkenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201915837
– volume: 40
  start-page: 3620
  year: 2020
  ident: WOS:000598969200007
  article-title: Photoinduced Decatungstate-Catalyzed C-H Functionalization
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc202006068
– volume: 58
  start-page: 8628
  year: 2019
  ident: WOS:000474806700001
  article-title: N-Heterocyclic Carbene Catalyzed Radical Coupling of Aldehydes with Redox-Active Esters
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201902792
– volume: 41
  start-page: 871
  year: 2021
  ident: WOS:000634840300045
  article-title: Visible-Light-Driven Sulfonamide Catalyzed Alkylation of alpha-C(sp(3))-H Bonds of Heteroatoms
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc202100016
– volume: 85
  start-page: 14744
  year: 2020
  ident: WOS:000592978100044
  article-title: Visible-Light-Induced Phosphorylation of Imidazo-Fused Heterocycles under Metal-Free Conditions
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.0c02107
– volume: 21
  start-page: 5728
  year: 2019
  ident: WOS:000476957200074
  article-title: Visible-Light-Induced Copper-Catalyzed Decarboxylative Coupling of Redox-Active Esters with N-Heteroarenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b02105
– volume: 11
  start-page: 1640
  year: 2021
  ident: WOS:000618540300051
  article-title: Single Electron Transfer-Induced Redox Processes Involving N-(Acyloxy)phthalimides
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.0c04756
– volume: 58
  start-page: 8572
  year: 2019
  ident: WOS:000476608700051
  article-title: Rapid Assessment of the Reaction-Condition-Based Sensitivity of Chemical Transformations
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201901935
– volume: 56
  start-page: 503
  year: 2020
  ident: WOS:000506632200001
  article-title: Photoinduced deaminative strategies: Katritzky salts as alkyl radical precursors
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc08348k
– volume: 19
  start-page: 3379
  year: 2021
  ident: WOS:000634379700001
  article-title: Copper(i)-catalyzed [4+2] cycloaddition of aza-ortho-quinone methides with bicyclic alkenes
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/d1ob00319d
– volume: 63
  start-page: 637
  year: 2020
  ident: WOS:000524185600001
  article-title: A review of enantioselective dual transition metal/photoredox catalysis
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-019-9701-5
– volume: 7
  start-page: 2531
  year: 2020
  ident: WOS:000562454200020
  article-title: Photoinduced strategies towards strained molecules
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/d0qo00460j
– volume: 97
  start-page: 419
  year: 2015
  ident: WOS:000356734600036
  article-title: Structure activity relationship (SAR) study of benzimidazole scaffold for different biological activities: A mini-review
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2014.11.053
– volume: 21
  start-page: 3436
  year: 2019
  ident: WOS:000471798100019
  article-title: Ambient and aerobic carbon-carbon bond cleavage toward alpha-ketoester synthesis by transition-metal-free photocatalysis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc01357a
– volume: 138
  start-page: 2174
  year: 2016
  ident: WOS:000371103900026
  article-title: Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b00250
– 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: 55
  start-page: 14637
  year: 2019
  ident: WOS:000501150200016
  article-title: The photoredox alkylarylation of styrenes with alkyl N-hydroxyphthalimide esters and arenes involving C-H functionalization
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc07494e
– volume: 86
  start-page: 1012
  year: 2021
  ident: WOS:000606840200083
  article-title: Visible-Light-Promoted Polysubstituted Olefins Synthesis Involving Sulfur Ylides as Carbene Trapping Reagents
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.0c02500
– volume: 56
  start-page: 11673
  year: 2020
  ident: WOS:000574031500024
  article-title: Electrochemical decarboxylative C3 alkylation of quinoxalin-2(1H)-ones withN-hydroxyphthalimide esters
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/d0cc05391k
– volume: 23
  start-page: 2353
  year: 2021
  ident: WOS:000631439700074
  article-title: Photoredox/Hydrogen Atom Transfer Cocatalyzed C-H Difluoroallylation of Amides, Ethers, and Alkyl Aldehydes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.1c00546
– 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: 23
  start-page: 232
  year: 2021
  ident: WOS:000608623000007
  article-title: Recent advances in visible-light-mediated organic transformations in water
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc03447a
– volume: 362
  start-page: 1947
  year: 2020
  ident: WOS:000531612200003
  article-title: Oxidative Radical Relay Functionalization for the Synthesis of Benzimidazo[2,1-a]iso-quinolin-6(5H)-ones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.202000040
– volume: 56
  start-page: 2495
  year: 2020
  ident: WOS:000519582800024
  article-title: Photocatalytic decarboxylative alkenylation of alpha-amino and alpha-hydroxy acid-derived redox active esters by NaI/PPh3 catalysis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc09654j
– volume: 143
  start-page: 964
  year: 2021
  ident: WOS:000612557200048
  article-title: 4CzIPN-Bu-t-Catalyzed Proton-Coupled Electron Transfer for Photosynthesis of Phosphorylated N-Heteroaromatics
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.0c11138
– volume: 113
  start-page: 3516
  year: 2013
  ident: WOS:000318892600017
  article-title: The Lipophilic Bullet Hits the Targets: Medicinal Chemistry of Adamantane Derivatives
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr100264t
– volume: 6
  start-page: 17252
  year: 2018
  ident: WOS:000452344900140
  article-title: Metal-Free Visible-Light-Induced C-H/C-H Cross-Dehydrogenative-Coupling of Quinoxalin-2(H)-ones with Simple Ethers
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.8b04652
– volume: 8
  start-page: 760
  year: 2021
  ident: WOS:000620718900014
  article-title: Visible-light-induced metal-free cascade cyclization of N-arylpropiolamides to 3-phosphorylated, trifluoromethylated and thiocyanated azaspiro[4.5]trienones
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/d0qo01410a
– volume: 45
  start-page: 3762
  year: 2010
  ident: WOS:000281568600029
  article-title: Synthesis and toxicity towards normal and cancer cell lines of benzimidazolequinones containing fused aromatic rings and 2-aromatic ring substituents
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2010.05.025
– volume: 31
  start-page: 3083
  year: 2020
  ident: WOS:000600917100014
  article-title: Recent advances for the photoinduced C-C bond cleavage of cycloketone oximes
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2020.07.035
– volume: 8
  start-page: 445
  year: 2021
  ident: WOS:000616326200002
  article-title: Nitriles as radical acceptors in radical cascade reactions
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/d0qo01058h
– volume: 17
  start-page: 9627
  year: 2019
  ident: WOS:000498709600009
  article-title: Metal-free oxidative acylation/cyclization of N-methacryloyl-2-phenylbenzoimidazole with aryl aldehydes: an easy access to benzimidazo[2,1-a]isoquinolin-6(5H)-ones
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c9ob01979k
– volume: 57
  start-page: 12270
  year: 2018
  ident: WOS:000444225100005
  article-title: Green and Rapid Hydrothermal Crystallization and Synthesis of Fully Conjugated Aromatic Compounds
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201801277
– volume: 10
  start-page: 6676
  year: 2020
  ident: WOS:000543663800008
  article-title: Mn-Catalyzed Electrochemical Radical Cascade Cyclization toward the Synthesis of Benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one Derivatives
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.0c01324
– volume: 35
  start-page: 2541
  year: 2015
  ident: WOS:000357457900014
  article-title: Pharmacological Induction of Human Fetal Globin Gene in Hydroxyurea-Resistant Primary Adult Erythroid Cells
  publication-title: MOLECULAR AND CELLULAR BIOLOGY
  doi: 10.1128/MCB.00035-15
– volume: 361
  start-page: 5176
  year: 2019
  ident: WOS:000497150900013
  article-title: Metal-Free Visible-Light Promoted Radical Cyclization to Access Perfluoroalkyl-Substituted Benzimidazo[2,1-a]isoquinolin-6(5H)-ones and Indolo[2,1-a]isoquinolin-6(5H)-ones
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201901016
– volume: 49
  start-page: 5263
  year: 2017
  ident: WOS:000418282000001
  article-title: Recent Progress on Radical Decarboxylative Alkylation for Csp(3)-C Bond Formation
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0036-1590935
– volume: 19
  start-page: 619
  year: 2021
  ident: WOS:000612478400014
  article-title: Peroxide-mediated synthesis of benzimidazo[2,1-a]isoquinoline-6(5H)-ones via cascade methylation/ethylation and intramolecular cyclization
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/d0ob02383c
– volume: 85
  start-page: 6888
  year: 2020
  ident: WOS:000538764000007
  article-title: Metal-Free Trifluoroalkylation of Quinoxalin-2(1H)-ones with Unactivated Alkenes and Langlois' Reagent
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.9b03505
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Snippet A visible-light-induced decarboxylation reaction was developed for the synthesis of alkylated benzimidazo­[2,1-a]­isoquinoline-6­(5H)-ones and...
A visible-light-induced decarboxylation reaction was developed for the synthesis of alkylated benzimidazo[2,1-a]isoquinoline-6(5H)-ones and...
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SubjectTerms Chemistry
Chemistry, Organic
decarboxylation
organic chemistry
photosynthesis
Physical Sciences
Science & Technology
volatile organic compounds
Title Metal-Free Photosynthesis of Alkylated Benzimidazo[2,1‑a]isoquinoline-6(5H)‑ones and Indolo[2,1‑a]isoquinolin-6(5H)‑ones in PEG-200
URI http://dx.doi.org/10.1021/acs.joc.1c01022
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