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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2008 Volume 18, Issue 1, Pages 48–50 (Mi mendc3242)

This article is cited in 3 papers

Chemo- and stereodirectivity of the reaction of thiocarbohydrazide with 1-acetyl-2-phenylacetylene: synthesis and structure of bis(1-methyl-3-phenyl-2-propynylidene)carbonothioic dihydrazide

M. Yu. Dvorkoa, T. E. Glotovaa, A. I. Albanova, N. N. Chipaninaa, O. N. Kazhevab, G. V. Shilovb, O. A. Dyachenkob

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation

Abstract: 1-Acetyl-2-phenylacetylene reacts with thiocarbohydrazide under mild conditions to afford exclusively N2-(Z-s-trans), N3-(Z-s-cis)- bis(1-methyl-3-phenyl-2-propynylidene)carbonothioic dihydrazide in high yield (up to 92%); the structure of the compound has been confirmed by IR and NMR spectroscopy and X-ray analysis.

Language: English

DOI: 10.1016/j.mencom.2008.01.018



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