Diastereoselective synthesis of triacetyl-L-erythro-C18-sphingosine

DOI: 10.1248/cpb.44.636

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 636 - 638 (1996)

Update date:2022-08-03

Topics:

Authors:

Miyata Miyata

Yamaguchi

Ninomiya

Naito Naito

Okamura Okamura

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Article abstract of DOI:10.1248/cpb.44.636

A new stereoselective synthetic route to triacetyl-L-erythro-C18- sphingosine has been developed by the combination of diastereoselective addition of thiophenol to chiral olefins and subsequent intramolecular substitution of the corresponding sulfonium group.

Full text of DOI:10.1248/cpb.44.636

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