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Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes

Recently discovered reactivity of nitrostyrenes in phosphorous acid to facilitate the diastereoselective [4 + 1]-cycloaddition of indoles in combination with unusual oxazoline ring cleavage and subsequent 1,2-alkyl shift afforded stereochemically defined 2-(3-oxoindolin-2-yl)-2-arylacetonitriles as...

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Главные авторы: Aksenov, A. V., Аксенов, А. В., Aksenov, D. A., Аксенов, Д. А., Aksenov, N. A., Аксенов, Н. А., Aleksandrova, E. V., Александрова, Е. В., Rubin, M. A., Рубин, М. А.
Формат: Статья
Язык:English
Опубликовано: American Chemical Society 2019
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Online-ссылка:https://dspace.ncfu.ru/handle/20.500.12258/8015
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spelling ir-20.500.12258-80152025-02-13T12:42:58Z Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes Aksenov, A. V. Аксенов, А. В. Aksenov, D. A. Аксенов, Д. А. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. V. Александрова, Е. В. Rubin, M. A. Рубин, М. А. Chemistry Diastereoselective Nitroalkenes One-pot reaction Oxazoline ring Phosphorous acid Organic compounds Recently discovered reactivity of nitrostyrenes in phosphorous acid to facilitate the diastereoselective [4 + 1]-cycloaddition of indoles in combination with unusual oxazoline ring cleavage and subsequent 1,2-alkyl shift afforded stereochemically defined 2-(3-oxoindolin-2-yl)-2-arylacetonitriles as sole products 2019-10-23T14:16:56Z 2019-10-23T14:16:56Z 2019 Статья Aksenov, A.V., Aksenov, D.A., Aksenov, N.A., Aleksandrova, E.V., Rubin, M. Preparation of Stereodefined 2-(3-Oxoindolin-2-yl)-2-Arylacetonitriles via One-Pot Reaction of Indoles with Nitroalkenes // Journal of Organic Chemistry. - 2019. - Volume 84. - Issue 19. - Pages 12420-12429 http://hdl.handle.net/20.500.12258/8015 en Journal of Organic Chemistry application/pdf application/pdf American Chemical Society
institution СКФУ
collection Репозиторий
language English
topic Chemistry
Diastereoselective
Nitroalkenes
One-pot reaction
Oxazoline ring
Phosphorous acid
Organic compounds
spellingShingle Chemistry
Diastereoselective
Nitroalkenes
One-pot reaction
Oxazoline ring
Phosphorous acid
Organic compounds
Aksenov, A. V.
Аксенов, А. В.
Aksenov, D. A.
Аксенов, Д. А.
Aksenov, N. A.
Аксенов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Rubin, M. A.
Рубин, М. А.
Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
description Recently discovered reactivity of nitrostyrenes in phosphorous acid to facilitate the diastereoselective [4 + 1]-cycloaddition of indoles in combination with unusual oxazoline ring cleavage and subsequent 1,2-alkyl shift afforded stereochemically defined 2-(3-oxoindolin-2-yl)-2-arylacetonitriles as sole products
format Статья
author Aksenov, A. V.
Аксенов, А. В.
Aksenov, D. A.
Аксенов, Д. А.
Aksenov, N. A.
Аксенов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Rubin, M. A.
Рубин, М. А.
author_facet Aksenov, A. V.
Аксенов, А. В.
Aksenov, D. A.
Аксенов, Д. А.
Aksenov, N. A.
Аксенов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Rubin, M. A.
Рубин, М. А.
author_sort Aksenov, A. V.
title Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
title_short Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
title_full Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
title_fullStr Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
title_full_unstemmed Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
title_sort preparation of stereodefined 2-(3-oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
publisher American Chemical Society
publishDate 2019
url https://dspace.ncfu.ru/handle/20.500.12258/8015
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