Studies on the selectivity between nickel-catalyzed 1,2- cis -2-Amino glycosylation of hydroxyl groups of thioglycoside acceptors with C(2)-Substituted benzylidene N -Phenyl trifluoroacetimidates and intermolecular aglycon transfer of the sulfide group

Journal of Organic Chemistry

Volumn 77, Issue 17, 2012, Pages 7330-7343

  Yu, Fei ^a   Nguyen, Hien M ^a  

^a University of Iowa   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANOMERICS; BENZYLIDENE; COUPLING ITERATION; DERIVATIZATIONS; GLYCOCONJUGATES; GLYCOSIDIC BOND; GLYCOSIDIC LINKAGES; GLYCOSYL ACCEPTORS; GLYCOSYL DONORS; GLYCOSYLATION REACTIONS; HYDROXYL GROUPS; NICKEL CATALYST; SELECTIVE DEPROTECTION; STEREOSELECTIVE SYNTHESIS; THIOGLYCOSIDES;

CARBOHYDRATES; CATALYSIS; ESTERIFICATION; GLYCOSYLATION; STEREOCHEMISTRY; STEREOSELECTIVITY;

SULFUR COMPOUNDS;

AGLYCONE; BENZYLIDENE N PHENYL TRIFLUOROACETIMIDATE; NICKEL; SULFIDE; THIOGLYCOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; GLYCOSYLATION; STEREOCHEMISTRY;

BENZYLIDENE COMPOUNDS; CATALYSIS; DISACCHARIDES; GLYCOSYLATION; HYDROXIDES; IMIDOESTERS; MOLECULAR CONFORMATION; NICKEL; ORGANOMETALLIC COMPOUNDS; SULFIDES; THIOGLYCOSIDES;

EID: 84866092796     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301050q     Document Type: Article

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