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Volumn 337, Issue 8, 2002, Pages 765-774
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Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?
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Author keywords
Conformational analysis; Density functional theory; Glycosylation; Stereoselectivity
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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;
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EID: 0037123262
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/S0008-6215(02)00043-5 Document Type: Article |
Times cited : (107)
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References (67)
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