Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/3436
Title: Direct reductive coupling of indoles to nitrostyrenes en route to (indol-3-yl)acetamides
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: Anticancer drug;En-route;One-pot method;Polyphosphoric acids;Reductive couplings
Issue Date: 2016
Publisher: Royal Society of Chemistry
Citation: Aksenov, A.V., Aksenov, N.A., Dzhandigova, Z.V., Aksenov, D.A., Voskressensky, L.G., Nenajdenko, V.G., Rubin, M. Direct reductive coupling of indoles to nitrostyrenes en route to (indol-3-yl)acetamides // RSC Advances. - 2016. - Volume 6. - 2016. - Issue 96. - Pages 93881-93886
Series/Report no.: RSC Advances
Abstract: A highly efficient one-pot method for the reductive coupling of indoles to nitrostyrenes in polyphosphoric acid doped with PCl3 was developed. This method allows direct and expeditious access to primary (indol-3-yl)acetamides, interesting as anti-cancer drug candidates
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-84991336276&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=f2513aeb9baa9b141865ee13207ae43d&sot=afnl&sdt=sisr&cluster=scopubyr%2c%222016%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Direct+reductive+coupling+of+indoles+to+nitrostyrenes+en+route+to%29&relpos=0&citeCnt=1&searchTerm=
http://hdl.handle.net/20.500.12258/3436
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