One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles

A highly efficient and expeditious one-pot approach towards 2-(3-oxoindolin-2-yl)acetonitriles was designed, which involves a base-assisted aldol reaction of ortho-nitroacetophenones, followed by hydrocyanation, triggering an unusual reductive cyclization reaction.

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Главные авторы:	Aksenov, N. A., Аксенов, Н. А., Aksenov, A. V., Аксенов, А. В., Kurenkov, I. A., Куренков, И. А., Kirilov, N. K., Кирилов, Н. К., Aksenov, D. A., Аксенов, Д. А., Arutiunov, N. A., Арутюнов, Н. А., Aksenova, D. S., Аксенова, Д. С., Rubin, M. A., Рубин, М. А.
Формат:	Статья
Язык:	English
Опубликовано:	MDPI 2022
Темы:	Brønsted acid catalysis Cascade transformations Indoles Nitroalkanes Rearrangements
Online-ссылка:	https://dspace.ncfu.ru/handle/20.500.12258/19606
Метки:	Добавить метку Нет меток, Требуется 1-ая метка записи!

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record_format	dspace
spelling	ir-20.500.12258-196062025-03-06T12:33:31Z One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles Aksenov, N. A. Аксенов, Н. А. Aksenov, A. V. Аксенов, А. В. Kurenkov, I. A. Куренков, И. А. Kirilov, N. K. Кирилов, Н. К. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenova, D. S. Аксенова, Д. С. Rubin, M. A. Рубин, М. А. Brønsted acid catalysis Cascade transformations Indoles Nitroalkanes Rearrangements A highly efficient and expeditious one-pot approach towards 2-(3-oxoindolin-2-yl)acetonitriles was designed, which involves a base-assisted aldol reaction of ortho-nitroacetophenones, followed by hydrocyanation, triggering an unusual reductive cyclization reaction. 2022-05-25T07:08:58Z 2022-05-25T07:08:58Z 2022 Статья Aksenov, N. A., Aksenov, A. V., Kurenkov, I. A., Kirillov, N. K., Aksenov, D. A., Arutiunov, N. A., Aksenova, D. S., Rubin, M. One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles // Molecules. - 2022. - Том 27. - Выпуск 9. - Номер статьи 2808. - DOI10.3390/molecules27092808 http://hdl.handle.net/20.500.12258/19606 en Molecules application/pdf application/pdf MDPI
institution	СКФУ
collection	Репозиторий
language	English
topic	Brønsted acid catalysis Cascade transformations Indoles Nitroalkanes Rearrangements
spellingShingle	Brønsted acid catalysis Cascade transformations Indoles Nitroalkanes Rearrangements Aksenov, N. A. Аксенов, Н. А. Aksenov, A. V. Аксенов, А. В. Kurenkov, I. A. Куренков, И. А. Kirilov, N. K. Кирилов, Н. К. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenova, D. S. Аксенова, Д. С. Rubin, M. A. Рубин, М. А. One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
description	A highly efficient and expeditious one-pot approach towards 2-(3-oxoindolin-2-yl)acetonitriles was designed, which involves a base-assisted aldol reaction of ortho-nitroacetophenones, followed by hydrocyanation, triggering an unusual reductive cyclization reaction.
format	Статья
author	Aksenov, N. A. Аксенов, Н. А. Aksenov, A. V. Аксенов, А. В. Kurenkov, I. A. Куренков, И. А. Kirilov, N. K. Кирилов, Н. К. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenova, D. S. Аксенова, Д. С. Rubin, M. A. Рубин, М. А.
author_facet	Aksenov, N. A. Аксенов, Н. А. Aksenov, A. V. Аксенов, А. В. Kurenkov, I. A. Куренков, И. А. Kirilov, N. K. Кирилов, Н. К. Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Aksenova, D. S. Аксенова, Д. С. Rubin, M. A. Рубин, М. А.
author_sort	Aksenov, N. A.
title	One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
title_short	One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
title_full	One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
title_fullStr	One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
title_full_unstemmed	One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
title_sort	one-pot synthesis of (e)-2-(3-oxoindolin-2-ylidene)-2-arylacetonitriles
publisher	MDPI
publishDate	2022
url	https://dspace.ncfu.ru/handle/20.500.12258/19606
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One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles

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