Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/3682
Title: Nitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitriles
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Dzhandigova, Z. V.
Джандигова, З. В.
Aksenov, D. A.
Аксенов, Д. А.
Rubin, M. A.
Рубин, М. А.
Keywords: Synthesis (chemical);One-pot synthesis;Nitroalkenes;Synthetic equivalents;Electrophilic functionalization
Issue Date: 2015
Publisher: Royal Society of Chemistry
Citation: Aksenov, A.V., Aksenov, N.A., Dzhandigova, Z.V., Aksenov, D.A., Rubin, M. Nitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitriles // RSC Advances. - 2015. - Volume 5. - Issue 129. - Pages 106492-106497
Series/Report no.: RSC Advances
Abstract: Nitroalkenes were used as synthetic equivalents of the cyanomethylium cation in a modular, one-pot synthesis of 2-(3-indolyl)acetonitriles and 2,2-diarylacetonitriles involving electrophilic functionalization of aromatic and heteroaromatic C-H bond
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-84951746246&origin=resultslist&sort=plf-f&src=s&nlo=&nlr=&nls=&sid=e87b5b6bf402771da295ad346bab27e9&sot=aff&sdt=cl&cluster=scopubyr%2c%222015%22%2ct&sl=174&s=AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29+OR+AF-ID%28%22Stavropol+State+University%22+60070961%29+OR+AF-ID%28%22stavropolskij+Gosudarstvennyj+Tehniceskij+Universitet%22+60026323%29&relpos=2&citeCnt=6&searchTerm=
http://hdl.handle.net/20.500.12258/3682
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
WoS 424 .pdf357.12 kBAdobe PDFThumbnail
View/Open
scopusresults 649 .pdf63.43 kBAdobe PDFThumbnail
View/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.