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Reductive activation of arenecarbonitriles for the reactions with some carbon-centered electrophiles: the reaction mechanisms and synthetic applications Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2008, Volume: 57, Number: 4, Pages: 768-779 Pages count : DOI: 10.1007/s11172-008-0116-6
Tags arenecarbonitriles; radical anions; dianions; cyanocyclohexadienyl anions; reductive alkylation and arylation; nucleophilic substitution; electron transfer
Authors Vaganova T. A. , Panteleeva E. V. , Shteingarts V. D.
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Abstract: Synthetic and mechanistic aspects of the developed approach to the activation of aromatic nitriles are considered. The approach is based on the transformation of aromatic nitriles into stable anionic reduced forms. The latter, as shown for the reactions with alkyl halides and cyanoarenes, are promising reactants for the reactions with carbon-centered electrophiles.
Cite: Vaganova T.A. , Panteleeva E.V. , Shteingarts V.D.
Reductive activation of arenecarbonitriles for the reactions with some carbon-centered electrophiles: the reaction mechanisms and synthetic applications
Russian Chemical Bulletin. 2008. V.57. N4. P.768-779. DOI: 10.1007/s11172-008-0116-6 WOS Scopus РИНЦ OpenAlex
Original: Ваганова Т.А. , Пантелеева Е.В. , Штейнгарц В.Д.
Восстановительная активация аренкарбонитрилов для взаимодействия с некоторыми углерод-центрированными электрофилами: механизм реакций и синтетические приложения
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2008. №4. С.754-765. РИНЦ
Dates:
Published print: Apr 1, 2008
Published online: Apr 15, 2009
Identifiers:
Web of science: WOS:000264400900006
Scopus: 2-s2.0-64949123328
Elibrary: 13582183
OpenAlex: W1983910337
Citing:
DB Citing
Web of science 12
Scopus 11
Elibrary 11
OpenAlex 11
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