Please use this identifier to cite or link to this item: http://hdl.handle.net/10995/51481
Title: Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles
Authors: Barabanov, M. A.
Sevenard, D. V.
Sosnovskikh, V. Ya.
Issue Date: 2012
Citation: Barabanov M. A. Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles / M. A. Barabanov, D. V. Sevenard, V. Ya. Sosnovskikh // Russian Chemical Bulletin. — 2012. — Vol. 61. — № 11. — P. 2183-2185.
Abstract: 1,4-Nucleophilic addition reactions of 3-nitrothiochromone with indoles gave a number of novel trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones in 36-89% yields. During the reactions, the thiopyrone ring underwent no opening. © 2012 Springer Science+Business Media New York.
Keywords: 2-(INDOL-3-YL)-3- NITROTHIO-CHROMAN-4-ONES
3-NITROTHIOCHROMONE
INDOLES
THE MICHAEL ADDITION
URI: http://hdl.handle.net/10995/51481
metadata.dc.rights: info:eu-repo/semantics/restrictedAccess
SCOPUS ID: 84884241892
WOS ID: WOS:000322877300025
PURE ID: 1072825
ISSN: 1066-5285
DOI: 10.1007/s11172-012-0308-y
Appears in Collections:Научные публикации, проиндексированные в SCOPUS и WoS

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