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Synthesis of 3-Fluoroindoles via Photoredox Catalysis Full article

Journal Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263
Output data Year: 2017, Volume: 82, Number: 1, Pages: 745-753 Pages count : 9 DOI: 10.1021/acs.joc.6b02344
Authors Panferova Liubov I. 1 , Smirnov Vladimir O. 1 , Levin Vitalij V. 1 , Kokorekin Vladimir A. 2,1 , Struchkova Marina I. 1 , Dilman Alexander D. 1
Affiliations
1 N.панD. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russian Federation
2 First I. M. Sechenov Moscow State Medical University, Trubetskaya st. 8-2, 119991 Moscow, Russian Federation

Abstract: A method for the synthesis of 3-fluoroindoles from N-arylamines substituted with the CF2I group is described. The reaction is mediated by a ruthenium photocatalyst in the presence of a substoichiometric amount of triphenylphosphine upon irradiation with blue light. The starting N-arylamines are readily obtained by nucleophilic iododifluoromethylation of iminium ions.
Cite: Panferova L.I. , Smirnov V.O. , Levin V.V. , Kokorekin V.A. , Struchkova M.I. , Dilman A.D.
Synthesis of 3-Fluoroindoles via Photoredox Catalysis
Journal of Organic Chemistry. 2017. V.82. N1. P.745-753. DOI: 10.1021/acs.joc.6b02344 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000391781900074
Scopus: 2-s2.0-85018479835
OpenAlex: W2565238958
Citing:
DB Citing
OpenAlex 36
Scopus 34
Web of science 35
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