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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2002 Volume 12, Issue 2, Pages 63–64 (Mi mendc4093)

This article is cited in 4 papers

Nucleophilic addition of secondary nitro compounds to acetylene

B. F. Kukharev, V. K. Stankevich, G. R. Klimenko

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation

Abstract: The products of C-vinylation were prepared in 52–65% yield by the reaction of secondary nitroalkanes with acetylene in DMSO– KOH.

Language: English

DOI: 10.1070/MC2002v012n02ABEH001541



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