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Acetamidoglycosylation with Glycal Donors: A One-Pot Glycosidic Coupling with Direct Installation of the Natural C(2)-N-Acetylamino Functionality

✍ Scribed by Valeria Di Bussolo; Jing Liu; Larry G. Huffman Jr.; David Y. Gin

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 103 KB
Volume: 112
Category: Article
ISSN: 0044-8249
DOI: 10.1002/(sici)1521-3757(20000103)112:1<210::aid-ange210>3.0.co;2-u

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Acetamidoglycosylation with Glycal Donor

Acetamidoglycosylation with Glycal Donors: A One-Pot Glycosidic Coupling with Direct Installation of the Natural C(2)-N-Acetylamino Functionality

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The 2-N-acetylamino-2-deoxy class of carbohydrates is ubiquitous among biologically important complex oligosaccharides and glycoconjugates, including, inter alia, glycosaminoglycans, peptidoglycans, and blood group antigens. [1] As a result, the efficient preparation of this group of glycosides ##

ChemInform Abstract: Acetamidoglycosylat

ChemInform Abstract: Acetamidoglycosylation with Glycal Donors: A One-Pot Glycosidic Coupling with Direct Installation of the Natural C(2)-N-Acetylamino Functionality.

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