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Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis

A novel highly efficient preparative method for the synthesis of substituted indoles using conjugate addition of nucleophiles to 3-(2-nitrovinyl)indoles has been developed. The addition of nucleophiles generated in the presence of a base from CH acids was investigated. The studied reactions proceed...

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Главные авторы: Aksenov, A. V., Аксенов, А. В., Aksenov, N. A., Аксенов, Н. А., Skomorokhov, A. A., Скоморохов, А. А., Aksenova, I. V., Аксенова, И. В., Griaznov, G. D., Грязнов, Г. Д., Rubin, M. A., Рубин, М. А.
Формат: Статья
Язык:English
Опубликовано: Springer New York LLC 2018
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Online-ссылка:https://dspace.ncfu.ru/handle/20.500.12258/3297
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spelling ir-20.500.12258-32972025-02-13T10:15:10Z Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis Aksenov, A. V. Аксенов, А. В. Aksenov, N. A. Аксенов, Н. А. Skomorokhov, A. A. Скоморохов, А. А. Aksenova, I. V. Аксенова, И. В. Griaznov, G. D. Грязнов, Г. Д. Rubin, M. A. Рубин, М. А. Addition Indoles Michael reaction Nitroalkenes A novel highly efficient preparative method for the synthesis of substituted indoles using conjugate addition of nucleophiles to 3-(2-nitrovinyl)indoles has been developed. The addition of nucleophiles generated in the presence of a base from CH acids was investigated. The studied reactions proceed quickly and smoothly under the conditions of microwave activation and do not require protection of the indole nitrogen atom 2018-10-19T09:58:39Z 2018-10-19T09:58:39Z 2016 Статья Aksenov, A.V., Aksenov, N.A., Skomorokhov, A.A., Aksenova, I.V., Gryaznov, G.D., Voskressensky, L.G., Rubin, M.A. Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis // Chemistry of Heterocyclic Compounds. - 2016. - Volume 52. - Issue 11. - Pages 923-927 http://hdl.handle.net/20.500.12258/3297 en Chemistry of Heterocyclic Compounds application/pdf application/pdf Springer New York LLC
institution СКФУ
collection Репозиторий
language English
topic Addition
Indoles
Michael reaction
Nitroalkenes
spellingShingle Addition
Indoles
Michael reaction
Nitroalkenes
Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Skomorokhov, A. A.
Скоморохов, А. А.
Aksenova, I. V.
Аксенова, И. В.
Griaznov, G. D.
Грязнов, Г. Д.
Rubin, M. A.
Рубин, М. А.
Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
description A novel highly efficient preparative method for the synthesis of substituted indoles using conjugate addition of nucleophiles to 3-(2-nitrovinyl)indoles has been developed. The addition of nucleophiles generated in the presence of a base from CH acids was investigated. The studied reactions proceed quickly and smoothly under the conditions of microwave activation and do not require protection of the indole nitrogen atom
format Статья
author Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Skomorokhov, A. A.
Скоморохов, А. А.
Aksenova, I. V.
Аксенова, И. В.
Griaznov, G. D.
Грязнов, Г. Д.
Rubin, M. A.
Рубин, М. А.
author_facet Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Skomorokhov, A. A.
Скоморохов, А. А.
Aksenova, I. V.
Аксенова, И. В.
Griaznov, G. D.
Грязнов, Г. Д.
Rubin, M. A.
Рубин, М. А.
author_sort Aksenov, A. V.
title Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
title_short Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
title_full Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
title_fullStr Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
title_full_unstemmed Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
title_sort michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
publisher Springer New York LLC
publishDate 2018
url https://dspace.ncfu.ru/handle/20.500.12258/3297
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