Improved Synthesis of Phytosphingosine and Dihydrosphingosine from 3,4,6-Tri-O-benzyl-D-galactal
β Scribed by Youhong Niu; Xiaoping Cao; Xin-Shan Ye
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- German
- Weight
- 185 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
An efficient and facile synthesis of phytosphingosine and dihydrosphingosine derivatives is described with less steps and in improved overall yield (66β72%) starting from commercially available triβOβbenzylβDβgalactal. The key steps include Wittig reaction, Mitsunobu transformation, reduction, and deprotection.
π SIMILAR VOLUMES
Synthesis and Some Transformations of 2-Acetamido-5-amino-3,4,6-tri-O-benzyl-2,5-dideoxy-D-glucono-1,5-lactam. -The synthesis and transformations of the title compound (IV), a useful precursor of N-acetylglucosaminidase inhibitors, are presented. -(GRANIER, T.;