| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5226496 | Tetrahedron | 2008 | 6 Pages |
Abstract
A 5-N,7-O-oxazinanone derivative of a thiosialic acid ester has been synthesized and investigated for the effect of conformational restriction on glycosylation. The cyclic group is found to be powerfully disarming, but to have no beneficial effect on reaction stereoselectivity.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
David Crich, Baolin Wu,