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Addition of mercaptans to acetylenic γ-hydroxy ketones
Authors:A. S. Medvedeva  L. P. Safronova  M. G. Voronkov
Affiliation:(1) Irkutsk Institute of Organic Chemistry, Siberian Branch of the Academy of Sciences of the USSR, USSR
Abstract:Conclusions Both the nucleophilic and the free radical addition of n-butyl mercaptan to acetylenicgamma-hydroxy ketones (1,1-disubstituted derivatives of 2-pentyn-1-ol-4-one) lead to the formation of the corresponding 1,1-disubstituted derivatives of 2-butylthio-2-penten-1-ol-4-one in 41–65% yield.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1669–1670, July, 1973.
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