The allyl group for protection in carbohydrate chemistry. 17. Synthesis of propyl O-(3,6-di-O-methyl-β-D-glucopyranosyl)- (1→4)-O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1 → 2)-3-O-methyl-α-L-rhamnopyranoside: the oligosaccharide portion of the major serologically active glycolipid from Mycobacterium leprae
- 1 September 1985
- journal article
- research article
- Published by Elsevier in Chemistry and Physics of Lipids
- Vol. 38 (3) , 299-307
- https://doi.org/10.1016/0009-3084(85)90023-4
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
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