SCOPUS 정보 검색 플랫폼

Volumn 337, Issue 8, 2002, Pages 765-774

Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?

(3) Nukada, Tomoo a Bérces, Attila b Whitfield, Dennis M c

a INST OF PHYS AND CHEMICAL RESEARCH (Japan)

b Novartis Forschungsinstitut GmbH (Austria)

c NATIONAL RESEARCH COUNCIL CANADA (Canada)

Author keywords

Conformational analysis; Density functional theory; Glycosylation; Stereoselectivity

Indexed keywords

CONFORMATIONS; HYDROGEN BONDS; METHANOL; STEREOCHEMISTRY;

CONFORMERS;

CARBOHYDRATES;

4,6 BENZYLIDENEGLUCOSE; CARBOHYDRATE DERIVATIVE; CATION; GLUCOSE DERIVATIVE; METHANOL; PYRAN DERIVATIVE; ALKENE; OLIGOSACCHARIDE; PROPYLENE;

ARTICLE; CALCULATION; CONFORMATION; CONFORMATIONAL TRANSITION; DENSITY; GLYCOSYLATION; HYDROGEN BOND; HYPOTHESIS; MOLECULAR DYNAMICS; PRIORITY JOURNAL; STEREOCHEMISTRY; THEORETICAL STUDY; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALKENES; CARBOHYDRATE CONFORMATION; GLYCOSYLATION; MODELS, MOLECULAR; OLIGOSACCHARIDES; STEREOISOMERISM;

EID: 0037123262 PISSN: 00086215 EISSN: None Source Type: Journal
DOI: 10.1016/S0008-6215(02)00043-5 Document Type: Article

Times cited : (108)

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