Directed nucleophilic addition of phenoxides to cyclopropenes

The alkali metal-templated addition of aryloxides across the double bond of non-conjugated cyclopropenes is described. High cis-selectivity is achieved through a directing effect of a strategically positioned carboxamide functionality

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Главные авторы:	Aksenov, N. A., Аксенов, Н. А., Rubin, M. A., Рубин, М. А.
Формат:	Статья
Язык:	English
Опубликовано:	Royal Society of Chemistry 2018
Темы:	Alkali metals Carboxamides Cyclopropene Double bond Nucleophilic addition Templated Addition reaction
Online-ссылка:	https://dspace.ncfu.ru/handle/20.500.12258/2765
Метки:	Добавить метку Нет меток, Требуется 1-ая метка записи!

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spelling	ir-20.500.12258-27652025-02-12T12:52:38Z Directed nucleophilic addition of phenoxides to cyclopropenes Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. Alkali metals Carboxamides Cyclopropene Double bond Nucleophilic addition Templated Addition reaction The alkali metal-templated addition of aryloxides across the double bond of non-conjugated cyclopropenes is described. High cis-selectivity is achieved through a directing effect of a strategically positioned carboxamide functionality 2018-08-03T12:47:55Z 2018-08-03T12:47:55Z 2017 Статья Yamanushkin, P., Lu-Diaz, M., Edwards, A., Aksenov, N.A., Rubina, M., Rubin, M. Directed nucleophilic addition of phenoxides to cyclopropenes // Organic and Biomolecular Chemistry. - 2017. - Volume 15. - Issue 38. - Pages 8153-8165 http://hdl.handle.net/20.500.12258/2765 en Organic and Biomolecular Chemistry application/pdf application/pdf Royal Society of Chemistry
institution	СКФУ
collection	Репозиторий
language	English
topic	Alkali metals Carboxamides Cyclopropene Double bond Nucleophilic addition Templated Addition reaction
spellingShingle	Alkali metals Carboxamides Cyclopropene Double bond Nucleophilic addition Templated Addition reaction Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. Directed nucleophilic addition of phenoxides to cyclopropenes
description	The alkali metal-templated addition of aryloxides across the double bond of non-conjugated cyclopropenes is described. High cis-selectivity is achieved through a directing effect of a strategically positioned carboxamide functionality
format	Статья
author	Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А.
author_facet	Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А.
author_sort	Aksenov, N. A.
title	Directed nucleophilic addition of phenoxides to cyclopropenes
title_short	Directed nucleophilic addition of phenoxides to cyclopropenes
title_full	Directed nucleophilic addition of phenoxides to cyclopropenes
title_fullStr	Directed nucleophilic addition of phenoxides to cyclopropenes
title_full_unstemmed	Directed nucleophilic addition of phenoxides to cyclopropenes
title_sort	directed nucleophilic addition of phenoxides to cyclopropenes
publisher	Royal Society of Chemistry
publishDate	2018
url	https://dspace.ncfu.ru/handle/20.500.12258/2765
work_keys_str_mv	AT aksenovna directednucleophilicadditionofphenoxidestocyclopropenes AT aksenovna directednucleophilicadditionofphenoxidestocyclopropenes AT rubinma directednucleophilicadditionofphenoxidestocyclopropenes AT rubinma directednucleophilicadditionofphenoxidestocyclopropenes
_version_	1842245664509001728

Directed nucleophilic addition of phenoxides to cyclopropenes

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