Triazole-fused sugars from nitroalkene-containing C-glycosides by a tandem 1,3-dipolar cycloaddition and intramolecular Michael addition

Carbohydrate Research

Volumn 344, Issue 8, 2009, Pages 1024-1027

  Zou, Wei ^a   Bhasin, Milan ^a   Vembaiyan, Kannan ^a   Williams, Dean T ^a  

^a NATIONAL RESEARCH COUNCIL CANADA   (Canada)

Author keywords

C Glycoside; Cycloaddition; Michael addition; Nitroalkene; Synthesis; Triazole

Indexed keywords

C-GLYCOSIDE; MICHAEL ADDITION; NITROALKENE; SYNTHESIS; TRIAZOLE;

CYCLOADDITION; SODIUM; SUGAR (SUCROSE); SYNTHESIS (CHEMICAL);

NITROGEN COMPOUNDS;

2 (1,2 TRANS 2 NITROCYCLOHEXYL) 1,2,3 TRIAZOLO [4,5] CYCLOHEXANE; 4 (1 C ACETYLMETHYL 2,3 DI O BENZYL ALPHA BETA LEVO THREOFURANOSIDE) 2H 1,2,3 TRIAZOLE; 4 (1 C ACETYLMETHYL 2,3 DI O BENZYL ALPHA DEXTRO ERYTHROFURANOSIDE) 2H 1,2,3 TRIAZOLE; 4 (1 C ALLYL 2,3 DI O BENZYL ALPHA DEXTRO ERYTHROFURANOSIDE) 2H 1,2,3 TRIAZOLE; 6 ACETYLMETHYL 4,5 DI O BENZYL 3 HYDROXYPYRIDO[1,5 C] 1,2,3 TRIAZOLE; ALKENE DERIVATIVE; CARBOHYDRATE DERIVATIVE; GLYCOSIDE; SODIUM AZIDE; UNCLASSIFIED DRUG;

ARTICLE; CYCLOADDITION; MICHAEL ADDITION; PRIORITY JOURNAL; ROOM TEMPERATURE; SUBSTITUTION REACTION;

CYCLIZATION; GLYCOSIDES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; TRIAZOLES;

EID: 65449154686     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2009.03.007     Document Type: Article

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