Epoxidation of C-branched glycals: Unexpected stereochemical results and their theoretical rationale

Carbohydrate Research

Volumn 338, Issue 3, 2003, Pages 231-236

  Ernst, Christiane ^a   Piacenza, Manuel ^a   Grimme, Stefan ^a   Klaffke, Werner ^a,b  

^a UNIVERSITY OF MÜNSTER   (Germany)

^b UNILEVER RESEARCH VLAARDINGEN   (Netherlands)

Author keywords

BP density functional; C Branched sugars; Epoxidation; Glycal

Indexed keywords

STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EPOXIDATION;

CARBOHYDRATES;

4 O ACETYL 1,2 ANHYDRO 6 DEOXY 3 C METHYL ALPHA LEVO ALLOPYRANOSE; 4 O ACETYL 1,2 ANHYDRO 6 DEOXY 3 C METHYL BETA LEVO ALTROPYRANOSE; GLYCOSIDE; METHYL 4 O ACETYL 6 DEOXY 3 C METHYL ALPHA LEVO ALTROPYRANOSIDE; METHYL 4 O ACETYL 6 DEOXY 3 C METHYL BETA LEVO ALLOPYRANOSIDE; PYRANOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; EPOXIDATION; HYDROGEN BOND; PRIORITY JOURNAL; STEREOCHEMISTRY; THEORY;

CARBOHYDRATE CONFORMATION; EPOXY COMPOUNDS; GLYCOSIDES; MODELS, MOLECULAR; STEREOISOMERISM;

EID: 0037474023     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6215(02)00406-8     Document Type: Article

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