Пропуск в контексте

Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles

The recently discovered [4+1]-spirocyclization of nitroalkenes to indoles provided a convenient new approach to 2-(1H-indol-2-yl)acetonitriles. However, this reaction was complicated by the formation of inert 3-(2-nitroethyl)-1H-indole byproducts. Herein, we offer a workaround this problem that allo...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Aksenov, A. V., Аксенов, А. В., Aksenov, N. A., Аксенов, Н. А., Aleksandrova, E. V., Александрова, Е. В., Aksenov, D. A., Аксенов, Д. А., Grishin, I. Y., Гришин, И. Ю., Rubin, M. A., Рубин, М. А.
Формат: Статья
Язык:English
Опубликовано: MDPI 2021
Темы:
Online-ссылка:https://dspace.ncfu.ru/handle/20.500.12258/18235
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!
id ir-20.500.12258-18235
record_format dspace
spelling ir-20.500.12258-182352025-02-12T14:08:00Z Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles Aksenov, A. V. Аксенов, А. В. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. V. Александрова, Е. В. Aksenov, D. A. Аксенов, Д. А. Grishin, I. Y. Гришин, И. Ю. Rubin, M. A. Рубин, М. А. Nitroalkanes Cascade transformations Heterocycles 1,2-alkyl shift Rearrangements The recently discovered [4+1]-spirocyclization of nitroalkenes to indoles provided a convenient new approach to 2-(1H-indol-2-yl)acetonitriles. However, this reaction was complicated by the formation of inert 3-(2-nitroethyl)-1H-indole byproducts. Herein, we offer a workaround this problem that allows for effective transformation of the unwanted byproducts into acetonitrile target molecules. 2021-11-08T14:27:28Z 2021-11-08T14:27:28Z 2021 Статья Aksenov, A.V., Aksenov, N.A., Aleksandrova, E.V., Aksenov, D.A., Grishin, I.Yu., Sorokina, E.A., Wenger, A., Rubin, M. Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles // Molecules, - 2021. - Том 26. - Выпуск 20. - Номер статьи 6132. - DOI: 10.3390/molecules26206132 http://hdl.handle.net/20.500.12258/18235 en Molecules application/pdf application/pdf MDPI
institution СКФУ
collection Репозиторий
language English
topic Nitroalkanes
Cascade transformations
Heterocycles
1,2-alkyl shift
Rearrangements
spellingShingle Nitroalkanes
Cascade transformations
Heterocycles
1,2-alkyl shift
Rearrangements
Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Aksenov, D. A.
Аксенов, Д. А.
Grishin, I. Y.
Гришин, И. Ю.
Rubin, M. A.
Рубин, М. А.
Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles
description The recently discovered [4+1]-spirocyclization of nitroalkenes to indoles provided a convenient new approach to 2-(1H-indol-2-yl)acetonitriles. However, this reaction was complicated by the formation of inert 3-(2-nitroethyl)-1H-indole byproducts. Herein, we offer a workaround this problem that allows for effective transformation of the unwanted byproducts into acetonitrile target molecules.
format Статья
author Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Aksenov, D. A.
Аксенов, Д. А.
Grishin, I. Y.
Гришин, И. Ю.
Rubin, M. A.
Рубин, М. А.
author_facet Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Aleksandrova, E. V.
Александрова, Е. В.
Aksenov, D. A.
Аксенов, Д. А.
Grishin, I. Y.
Гришин, И. Ю.
Rubin, M. A.
Рубин, М. А.
author_sort Aksenov, A. V.
title Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles
title_short Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles
title_full Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles
title_fullStr Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles
title_full_unstemmed Direct conversion of 3-(2-nitroethyl)-1H-indoles into 2-(1H-indol-2-yl)acetonitriles
title_sort direct conversion of 3-(2-nitroethyl)-1h-indoles into 2-(1h-indol-2-yl)acetonitriles
publisher MDPI
publishDate 2021
url https://dspace.ncfu.ru/handle/20.500.12258/18235
work_keys_str_mv AT aksenovav directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aksenovav directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aksenovna directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aksenovna directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aleksandrovaev directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aleksandrovaev directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aksenovda directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT aksenovda directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT grishiniy directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT grišiniû directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT rubinma directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
AT rubinma directconversionof32nitroethyl1hindolesinto21hindol2ylacetonitriles
_version_ 1842245705787244544