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https://dspace.ncfu.ru/handle/20.500.12258/395
Title: | Intramolecular nucleophilic addition of carbanions generated from: N -benzylamides to cyclopropenes |
Authors: | Aksenov, N. A. Аксенов, Н. А. Rubin, M. A. Рубин, М. А. |
Keywords: | Addition reaction;Scaffolds;Carboxamides;Cyclopropene;Nucleophilic addition;Nucleophilic substitutions;Reaction intermediate |
Issue Date: | 2018 |
Publisher: | Royal Society of Chemistry |
Citation: | Maslivetc, V., Barrett, C., Aksenov, N.A., Rubina, M., Rubin, M. Intramolecular nucleophilic addition of carbanions generated from: N -benzylamides to cyclopropenes // Organic and Biomolecular Chemistry. - 2018. - Volume 16. - Issue 2. - pp. 285-294. |
Series/Report no.: | Organic and Biomolecular Chemistry |
Abstract: | An unusual reaction is described, involving a formal intramolecular nucleophilic substitution of bromocyclopropanes with nitrogen ylides generated in situ from N-benzyl carboxamides. It is shown that this reaction involves cyclopropene intermediates and allows for the facile and expeditious preparation of 3-azabicyclo[3.1.0]hexan-2-one scaffolds |
URI: | https://www.scopus.com/record/display.uri?eid=2-s2.0-85040323559&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=nort*+caucas*+fed*+univ*&sid=ebf9446ddab8c0101772b7f698064ac5&sot=afnl&sdt=afsp&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=55&citeCnt=1&searchTerm= https://dspace.ncfu.ru:443/handle/20.500.12258/395 |
Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
File | Description | Size | Format | |
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scopusresults (56).pdf Restricted Access | 61.64 kB | Adobe PDF | View/Open | |
WoS 16 .pdf Restricted Access | 78.2 kB | Adobe PDF | View/Open |
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