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Issue 12, 1991
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An enantio- and stereo-controlled synthesis of L-erythro- and D-threo-C18-sphingosines via the anomalous version of the katsuki–sharpless asymmetric epoxidation reaction

Abstract

A new enantiocontrolled synthesis of L-erythro- and D-threo-sphingosines has been established starting from (R,R)- and meso-1,2-divinylethylene glycols via the anomalous version of the Katsuki–Sharpless asymmetric epoxidation reaction as the key step.

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Article information


J. Chem. Soc., Chem. Commun., 1991, 820-821
Article type
Paper

An enantio- and stereo-controlled synthesis of L-erythro- and D-threo-C18-sphingosines via the anomalous version of the katsuki–sharpless asymmetric epoxidation reaction

S. Takano, Y. Iwabuchi and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1991, 820
DOI: 10.1039/C39910000820

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