Diastereoselective Synthesis of Triacetyl-L-erythro-C18-sphingosine.
- 1 January 1996
- journal article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 44 (3) , 636-638
- https://doi.org/10.1248/cpb.44.636
Abstract
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.Keywords
This publication has 0 references indexed in Scilit: