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Volumn 345, Issue 12, 2010, Pages 1713-1721

A highly α-selective glycosylation for the convenient synthesis of repeating α-(1→4)-linked N-acetyl-galactosamine units

(2) Yang, Lin a Ye, Xin Shan a

a NONE

Author keywords

(1 4) Linked N acetyl galactosamine; Stereoselectivity; Glycosylation; Oxazolidinone; Thioglycoside

Indexed keywords

BACTERIAL STRAINS; GALACTOSAMINE; GLYCOSYL DONORS; GLYCOSYLATION REACTIONS; ISOLATED YIELD; OXAZOLIDINONES; PRE-ACTIVATION; TERT-BUTYLDIMETHYLSILYL; THIOGLYCOSIDES;

ESTERIFICATION; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

GLYCOSYLATION;

ALPHA (1 4) LINKED N ACETYLGALACTOSAMINE; ASPARAGINE; BACTERIAL POLYSACCHARIDE; GLYCAN DERIVATIVE; THIOGLYCOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CAMPYLOBACTER JEJUNI; CARBOHYDRATE ANALYSIS; CONTROLLED STUDY; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; GLYCOSYLATION; PRIORITY JOURNAL; SPHAEROTILUS;

CARBOHYDRATE SEQUENCE; GALACTOSAMINE; GLYCOSYLATION; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; STEREOISOMERISM;

BACTERIA (MICROORGANISMS);

EID: 77955656016 PISSN: 00086215 EISSN: None Source Type: Journal
DOI: 10.1016/j.carres.2010.05.031 Document Type: Article

Times cited : (22)

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