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Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes

A new method for synthesizing 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed intramolecular electrophilic amination of 2-arylindole-3-carbaldehyde O-acetyl oximes was developed

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Главные авторы: Aksenov, N. A., Аксенов, Н. А., Gasanova, A. Z., Гасанова, А. З., Prokonov, F. Y., Проконов, Ф. Ю., Aksenov, D. A., Аксенов, Д. А., Aksenov, A. V., Аксенов, А. В.
Формат: Статья
Язык:English
Опубликовано: Springer 2020
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Online-ссылка:https://dspace.ncfu.ru/handle/20.500.12258/11431
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id ir-20.500.12258-11431
record_format dspace
spelling ir-20.500.12258-114312025-02-13T10:19:48Z Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes Aksenov, N. A. Аксенов, Н. А. Gasanova, A. Z. Гасанова, А. З. Prokonov, F. Y. Проконов, Ф. Ю. Aksenov, D. A. Аксенов, Д. А. Aksenov, A. V. Аксенов, А. В. Alkaloids Amination Indoloquinolines Quinoline A new method for synthesizing 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed intramolecular electrophilic amination of 2-arylindole-3-carbaldehyde O-acetyl oximes was developed 2020-02-18T12:11:26Z 2020-02-18T12:11:26Z 2019 Статья Aksenov, N.A., Gasanova, A.Z., Prokonov, F.Y., Aksenov, D.A., Abakarov, G.M., Aksenov, A.V. Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes // Russian Chemical Bulletin. - 2019. - Volume 68. - Issue 12. - Pages 2262-2270 http://hdl.handle.net/20.500.12258/11431 en Russian Chemical Bulletin application/pdf application/pdf Springer
institution СКФУ
collection Репозиторий
language English
topic Alkaloids
Amination
Indoloquinolines
Quinoline
spellingShingle Alkaloids
Amination
Indoloquinolines
Quinoline
Aksenov, N. A.
Аксенов, Н. А.
Gasanova, A. Z.
Гасанова, А. З.
Prokonov, F. Y.
Проконов, Ф. Ю.
Aksenov, D. A.
Аксенов, Д. А.
Aksenov, A. V.
Аксенов, А. В.
Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes
description A new method for synthesizing 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed intramolecular electrophilic amination of 2-arylindole-3-carbaldehyde O-acetyl oximes was developed
format Статья
author Aksenov, N. A.
Аксенов, Н. А.
Gasanova, A. Z.
Гасанова, А. З.
Prokonov, F. Y.
Проконов, Ф. Ю.
Aksenov, D. A.
Аксенов, Д. А.
Aksenov, A. V.
Аксенов, А. В.
author_facet Aksenov, N. A.
Аксенов, Н. А.
Gasanova, A. Z.
Гасанова, А. З.
Prokonov, F. Y.
Проконов, Ф. Ю.
Aksenov, D. A.
Аксенов, Д. А.
Aksenov, A. V.
Аксенов, А. В.
author_sort Aksenov, N. A.
title Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes
title_short Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes
title_full Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes
title_fullStr Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes
title_full_unstemmed Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes
title_sort synthesis of 11h-indolo[3,2-c]quinolines by sncl4-catalyzed cyclization of indole-3-carbaldehyde oximes
publisher Springer
publishDate 2020
url https://dspace.ncfu.ru/handle/20.500.12258/11431
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