Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/3297
Title: Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Skomorokhov, A. A.
Скоморохов, А. А.
Aksenova, I. V.
Аксенова, И. В.
Griaznov, G. D.
Грязнов, Г. Д.
Rubin, M. A.
Рубин, М. А.
Keywords: Addition;Indoles;Michael reaction;Nitroalkenes
Issue Date: 2016
Publisher: Springer New York LLC
Citation: Aksenov, A.V., Aksenov, N.A., Skomorokhov, A.A., Aksenova, I.V., Gryaznov, G.D., Voskressensky, L.G., Rubin, M.A. Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis // Chemistry of Heterocyclic Compounds. - 2016. - Volume 52. - Issue 11. - Pages 923-927
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: A novel highly efficient preparative method for the synthesis of substituted indoles using conjugate addition of nucleophiles to 3-(2-nitrovinyl)indoles has been developed. The addition of nucleophiles generated in the presence of a base from CH acids was investigated. The studied reactions proceed quickly and smoothly under the conditions of microwave activation and do not require protection of the indole nitrogen atom
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85015459545&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=b34ee1a283c2e8415711b601b248f06f&sot=afnl&sdt=cl&cluster=scopubyr%2c%222016%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=80&citeCnt=2&searchTerm=
http://hdl.handle.net/20.500.12258/3297
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