A Facile Stereoselective Synthesis of Sphingosine and Ceramide
β Scribed by Li, Yun-Long ;Wu, Yu-Lin
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 410 KB
- Volume
- 1996
- Category
- Article
- ISSN
- 0947-3440
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β¦ Synopsis
Abstract
Flexible syntheses of sphingosine and ceramide were achieved by using Dβxylose as the chiral pool and a CuCNβcatalyzed allylic alkylation reaction of a dimesylate 8 for chain elongation with concomitant control of an E configuration of the double bond.
π SIMILAR VOLUMES
A novel regioselective synthesis of D-erythro -sphingosine 1-phosphate and D-erythro -ceramide 1-phosphate is described. The synthesis is based upon (1) in situ oxidative phosphorylation of the primary hydroxyl group in N-Boc-D-erythro-sphingosine utilizing trimethyl phosphite and carbon tetrabromid
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