| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223970 | Tetrahedron | 2010 | 7 Pages |
Abstract
Two α-d-arabinofuranosyl oligosaccharides (2 and 3) found as constituent parts of the polysaccharide portion from the cell wall of Mycobacterium tuberculosis have been efficiently synthesized via a one-pot glycosylation procedure in which a key step is the chemoselective activation between d-arabinofuranosyl trichloroacetimidate donor 4 and partially protected aryl thioglycosides 5 or 7, respectively.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xing-Yong Liang, Li-Min Deng, Xia Liu, Jin-Song Yang,