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 |
Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
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scopusresults 205 .pdf Restricted Access | 62.48 kB | Adobe PDF | View/Open | |
WoS 96 .pdf Restricted Access | 758.14 kB | Adobe PDF | View/Open |
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