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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2007 Volume 17, Issue 3, Pages 181–182 (Mi mendc3419)

This article is cited in 15 papers

Free-radical addition of phosphine sulfides to aryl and hetaryl acetylenes: unprecedented stereoselectivity

B. A. Trofimova, S. F. Malyshevaa, N. K. Gusarovaa, N. A. Belogorlovaa, S. F. Vasilevskiib, V. B. Kobycheva, B. G. Sukhova, I. A. Ushakova

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b V.V. Voevodsky Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: Secondary phosphine sulfides react stereo- and regioselectively with aryl and hetaryl acetylenes in the presence of radical initiators (AIBN, 60–65 °C) in the anti-Markovnikov mode giving Z-isomers of the corresponding monoadducts in high yields.

Language: English

DOI: 10.1016/j.mencom.2007.05.017



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