Directed nucleophilic addition of phenoxides to cyclopropenes

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:	https://www.scopus.com/record/display.uri?eid=2-s2.0-85030682886&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=North+Caucasus+Federal+University&sid=a75f219f53d4022b97f1d2161feb9566&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Directed+nucleophilic+addition+of+phenoxides+to+cyclopropenes%29&relpos=2&citeCnt=2&searchTerm= http://hdl.handle.net/20.500.12258/2765
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