Stereoselective glycosylations using benzoylated glucosyl halides with inexpensive promoters

Carbohydrate Research

Volumn 343, Issue 8, 2008, Pages 1297-1308

  Murakami, Teiichi ^a   Sato, Yukari ^a   Shibakami, Motonari ^a  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

Author keywords

Anomer; Disarmed glycosyl halides; Glycosylation; Lewis acids; NBS

Indexed keywords

ALCOHOLS; GLUCOSE; GLYCOSYLATION; HALOGENATION; STEREOSELECTIVITY; ZINC COMPOUNDS;

ANOMERS; DISARMED GLYCOSYL HALIDES; LEWIS ACIDS;

CARBOHYDRATES;

12 BROMODODECYL 2,3,4,6 TETRA O BENZOYL ALPHA DEXTRO GLUCOPYRANOSIDE; 12 BROMODODECYL 2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSIDE; 2 PHENYLETHYL 2,3,4,6 TETRA O BENZOYL ALPHA DEXTRO GLUCOPYRANOSIDE; 2,3,4,6 TETRA O BENZOYL ALPHA DEXTRO GLUCOPYRANOSYL IODIDE; 2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSYL IODIDE; 3,4,6 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSE ORTHOESTER; 4 PENTENYL 2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSIDE; 6 O(2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSYL) 1,2:3,4 DI O ISOPROPYLIDENE ALPHA DEXTRO GALACTOPYRANOSE; ALCOHOL; CHOLEST 5 EN 3 BETA YL 2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSIDE; CYCLOHEXYL 2,3,4,6 TETRA O BENZOYL ALPHA DEXTRO GLUCOPYRANOSYL IODIDE; CYCLOHEXYL 2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSYL IODIDE; GLUCOPYRANOSYL HALIDE; GLUCOSE; HALIDE; IODINE DERIVATIVE; METHYL 2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSYL(1-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSIDE; METHYL 2,3,4,6-TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSYL(1-4) 2,3,6 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSIDE; N BEZYLOXYCARBONYL O(2,3,4,6 TETRA O BENZOYL BETA DEXTRO GLUCOPYRANOSYL)SERINE METHYL ESTER; N BROMOSUCCINIMIDE; TRIMETHYLSILYL HALIDE; ZINC HALIDE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; GLYCOSYLATION; HALOGENATION; PRIORITY JOURNAL; STEREOCHEMISTRY;

BROMIDES; BROMOSUCCINIMIDE; GLUCOSIDES; GLYCOSYLATION; HALOGENS; IODIDES; STEREOISOMERISM; ZINC COMPOUNDS;

EID: 43049151751     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2008.03.019     Document Type: Article

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