Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5221816 | Tetrahedron | 2011 | 10 Pages |
Abstract
A directing/protecting group designed for regioselective functionalization of partially-protected glucopyrannosides has been successfully used to prepare disaccharides in high yields. Most importantly, it has been demonstrated that highly regioselective and stereoselective glycosylation can be achieved when disarmed donors are employed. This study demonstrates the ability of directing/protecting group to induce regioselective glycosylation of carbohydrates and opens the field to the design of other DPGs for other monosaccharides.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Janice Lawandi, Sylvain Rocheleau, Nicolas Moitessier,