Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/2765
Title: Directed nucleophilic addition of phenoxides to cyclopropenes
Authors: Aksenov, N. A.
Аксенов, Н. А.
Rubin, M. A.
Рубин, М. А.
Keywords: Alkali metals;Carboxamides;Cyclopropene;Double bond;Nucleophilic addition;Templated;Addition reaction
Issue Date: 2017
Publisher: Royal Society of Chemistry
Citation: 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
Series/Report no.: Organic and Biomolecular Chemistry
Abstract: 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
URI: http://hdl.handle.net/20.500.12258/2765
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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