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Journal of the American Chemical Society

Volumn 123, Issue 28, 2001, Pages 6819-6825

Why are the hydroxy groups of partially protected N-acetylglucosamine derivatives such poor glycosyl acceptors, and what can be done about it? A comparative study of the reactivity of N-acetyl-, N-phthalimido-, and 2-azido-2-deoxy-glucosamine derivatives in glycosylation. 2-Picolinyl ethers as reactivity-enhancing replacements for benzyl ethers

(2) Crich, D a Dudkin, V a

a UNIVERSITY OF ILLINOIS AT CHICAGO (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSYLATION;

ATMOSPHERIC PRESSURE; ETHERS; HYDROGEN BONDS;

DERIVATIVES;

2 AZIDO 2 DEOXYGLUCOSAMINE DERIVATIVE; 3 O PICOLINYL 4 O BENZYL N ACETYLGLUCOSAMINE DERIVATIVE; 3 O PICOLINYL 6 O BENZYL N ACETYLGLUCOSAMINE DERIVATIVE; GLUCOSAMINE DERIVATIVE; N ACETYL N BENZYLGLUCOSAMINE DERIVATIVE; N ACETYLGLUCOSAMINE DERIVATIVE; N PHTHALIMIDOGLUCOSAMINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; GLYCOSYLATION; HYDROGEN BOND; REACTION ANALYSIS; SYNTHESIS;

ACETYLGLUCOSAMINE; AZIDES; BENZYL COMPOUNDS; BINDING, COMPETITIVE; ETHERS, CYCLIC; GLYCOSYLATION; METHYL ETHERS; PHTHALIMIDES; PICOLINES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0034835601 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja010086b Document Type: Article

Times cited : (208)

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