A new synthesis of α-arbutin via Lewis acid catalyzed selective glycosylation of tetra-O-benzyl-α-d-glucopyranosyl trichloroacetimidate with hydroquinone

Carbohydrate Research

Volumn 341, Issue 11, 2006, Pages 1945-1947

  Wang, Zhao Xia ^a   Shi, Xiao Xin ^a   Chen, Guo Rong ^a   Ren, Zhi Hua ^a   Luo, Lei ^a   Yan, Jing ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Arbutin; Glycosylation; Hydroquinone; Trichloracetimidate

Indexed keywords

ENZYME KINETICS; ENZYMES; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

Α-ARBUTIN; GLYCOSYLATION; HYDROQUINONE; TRICHLORACETIMIDATE;

CARBOHYDRATES;

ALPHA ARBUTIN; GLUCOPYRANOSIDE; HYDROQUINONE; LEWIS ACID; TETRAISOBENZYL ALPHA DEXTRO GLUCOPYRANOSYL TRICHLOROACETIMIDATE; TRICHLOROACETIMIDIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; DEPROTECTION REACTION; GLYCOSYLATION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

ACIDS; ARBUTIN; CATALYSIS; GLYCOSYLATION; HYDROQUINONES; MODELS, CHEMICAL; MOLECULAR STRUCTURE; TRICHLOROACETIC ACID;

TETRA;

EID: 33744980446     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2006.04.022     Document Type: Article

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