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Electrooxidation of tigogenin acetate
Authors:Jacek W Morzycki  Yliana Lpez  Jolanta P&#x;oszy&#x;ska  Rosa Santillan  Leszek Siergiejczyk  Andrzej Sobkowiak
Institution:aInstitute of Chemistry, University of Białystok, Piłsudskiego 11/4, 15-443 Białystok, Poland;bFaculty of Chemistry, Rzeszów University of Technology, P.O. Box 85, 35-959 Rzeszów, Poland;cDepartamento de Química, CINVESTAV-IPN, Apdo. Postal 14-740, 07000 Mexico, D.F., Mexico
Abstract:Electrooxidation of tigogenin acetate afforded two products: 3β-acetoxy-16β-hydroxy-23,24-dinor-5α-cholanoic acid lactone (2) and 20-epitigogenin acetate (3). The structure of the latter compound was confirmed by an X-ray analysis. The tentative mechanism of reaction is proposed.
Keywords:Saponins  Tigogenin  Electrochemical oxidation  Electrochemically-induced stereoisomerization
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