Gigg, J

The allyl group for protection in carbohydrate chemistry. 17. Synthesis of propyl O-(3,6-di-O-methyl-beta-D-glucopyranosyl)-(1----4)-O-(2,3- di-O-methyl-alpha-L-rhamnopyranosyl)-(1----2)-3-O-methyl-alpha- L-rhamnopyranoside: the oligosaccharide portion of the major serologically active glycolipid from Mycobacterium leprae. [electronic resource] - Chemistry and physics of lipids Sep 1985 - 299-307 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0009-3084

10.1016/0009-3084(85)90023-4 doi


Glycolipids--chemical synthesis
Indicators and Reagents
Mycobacterium leprae--immunology
Oligosaccharides--chemical synthesis
Optical Rotation
Trisaccharides--chemical synthesis