Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3682
Title: Nitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitriles
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Dzhandigova, Z. V.
Джандигова, З. В.
Aksenov, D. A.
Аксенов, Д. А.
Rubin, M. A.
Рубин, М. А.
Keywords: Synthesis (chemical);One-pot synthesis;Nitroalkenes;Synthetic equivalents;Electrophilic functionalization
Issue Date: 2015
Publisher: Royal Society of Chemistry
Citation: Aksenov, A.V., Aksenov, N.A., Dzhandigova, Z.V., Aksenov, D.A., Rubin, M. Nitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitriles // RSC Advances. - 2015. - Volume 5. - Issue 129. - Pages 106492-106497
Series/Report no.: RSC Advances
Abstract: Nitroalkenes were used as synthetic equivalents of the cyanomethylium cation in a modular, one-pot synthesis of 2-(3-indolyl)acetonitriles and 2,2-diarylacetonitriles involving electrophilic functionalization of aromatic and heteroaromatic C-H bond
URI: http://hdl.handle.net/20.500.12258/3682
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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