Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 70, Issue 20, Pages 8228-8230Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo051069y
Keywords
-
Categories
Ask authors/readers for more resources
The preparation of the glycosphingolipid galactosyl ceramide from an orthogonally protected five-carbon building block is described. The main chain of the lipid is installed via a highly stereoselective olefin cross metathesis reaction. The methodology permits the facile preparation of glycolipids which vary in the length of the main carbon chain.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available