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A facile stereoselective synthesis of sphingosine and ceramide

DOI: 10.1002/jlac.199619961219

Source and publish data:

Liebigs Annalen p. 2079 - 2082 (1996)

Update date:2022-08-05

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Authors:

Li, Yun-LongLi, Yun-Long

Wu, Yu-LinWu, Yu-Lin

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Article abstract of DOI:10.1002/jlac.199619961219

Flexible syntheses of sphingosine and ceramide were achieved by using D-xylose as the chiral pool and a CuCN-catalyzed allylic alkylation reaction of a dimesylate 8 for chain elongation with concomitant control of an E configuration of the double bond. VCH Verlagsgesellschaft mbH, 1996.

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Full text of DOI:10.1002/jlac.199619961219

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