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Cathodic isomerization of epoxysulfides -sulfoxides and -sulfones Full article

Journal Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581
Output data Year: 1991, Volume: 32, Number: 8, Pages: 1099-1102 Pages count : 4 DOI: 10.1016/s0040-4039(00)74498-4
Authors Niyazymbetov M.E. 1 , Konyushkin L.D. 1 , Niyazymbetova Z.I. 1 , Kalugin V.E. 1 , Litvinov V.P. 1 , Petrosyan V.A. 1
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry, USSR Academy of Sciences, Leninsky Prospekt 47, Moscow 117913, USSR

Abstract: It has been established that the electrolysis of 2,3-epoxypropylsulfides, -sulfoxides and -sulfones on Pt or glassy carbon cathodes proceeds via the cleavage of the αCH bond, followed by intramolecular interaction of the α-carbanion with epoxidic ring to give corresponding allylic alcohols in good yields. The electrolysis of 2,3-epoxypropylsulfides, -sulfoxides and -sulfones on Pt or glassy carbon cathodes leads to the formation of corresponding allylic alcohols in good yields.
Cite: Niyazymbetov M.E. , Konyushkin L.D. , Niyazymbetova Z.I. , Kalugin V.E. , Litvinov V.P. , Petrosyan V.A.
Cathodic isomerization of epoxysulfides -sulfoxides and -sulfones
Tetrahedron Letters. 1991. V.32. N8. P.1099-1102. DOI: 10.1016/s0040-4039(00)74498-4 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:A1991EZ57400032
≡ Scopus: 2-s2.0-0026059952
≡ OpenAlex: W2081682113
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