Synthesis of potential inhibitors of the glycosphingolipid biosynthesis
✍ Scribed by Gerald Brenner-Weiß; Athanassios Giannis; Konrad Sandhoff
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 523 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
A synthesis of ceramide analogs 6 and 7 is reported here starting from L-cysteine. Alkylation of 2 and subsequent reduction of the intermediate formed ketone 3 afforded the diitereomeric alcohols 4. Deprotection and acylation of 4 lead to the desired product 6 which is converted to the sulfonium salt 7. ~orn~o~d 6 is a powerful inhibiir of the gly~spb~iipid biosynthesis.
📜 SIMILAR VOLUMES
Simple synthetic routes arc described to 5,6\_dehydroarachidnnic acid (5). cis-8-eicosen-5-ynoic acid (6) and the thio analog of ('I-leukotriene A (71,which are of value in the study of ^ inhibition of the biosynthesis