SYNTHESIS OF (4E,8E,2S,3R,2'R)-N-2'-HYDROXYHEXADECANOYL-9-METHYL-4,8-SPHINGADIENINE, THE CERAMIDE PORTION OF THE FRUITING-INDUCING CEREBROSIDE IN A BASIDIOMYCETE SCHIZOPHYLLUM COMMUNE, AND ITS (2R,3S)-ISOMER

DOI: 10.1016/S0040-4020(01)96632-3

Source and publish data:

Tetrahedron p. 2369 - 2378 (1985)

Update date:2022-08-04

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Authors:

Mori, Kenji

Funaki, Yuji

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Article abstract of DOI:10.1016/S0040-4020(01)96632-3

A synthesis of the natural enantiomer as well as its diastereomer of the title compound was accomplished, confirming the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune.

Full text of DOI:10.1016/S0040-4020(01)96632-3

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