Revisit of the phenol O-glycosylation with glycosyl imidates, BF 3·OEt2 is a better catalyst than TMSOTf

Carbohydrate Research

Volumn 363, Issue , 2012, Pages 14-22

  Li, Yali ^a,b   Mo, Huaping ^a   Lian, Gaoyan ^a   Yu, Biao ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b TIANJIN UNIVERSITY   (China)

Author keywords

BF3 OEt 2; Glycosyl imidates; Phenol O glycosylation; TMSOTf

Indexed keywords

GLYCOSYL; IMIDATES; LOW TEMPERATURES; NUCLEOPHILICITIES; O-GLYCOSIDES; O-GLYCOSYLATION; OXOCARBENIUM; TMSOTF; TRICHLOROACETIMIDATES; TRIFLATES;

CATALYSTS; ESTERIFICATION; GLYCOSYLATION; SUGARS;

PHENOLS;

1,2 ORTHOESTER; BORON TRIFLUORIDE; BORON TRIFLUORIDE DIETHYL ETHER; ESTER; ETHER; GLYCOSIDE; GLYCOSYLATED PROTEIN; PHENOL; TRIFLUOROMETHANESULFONIC ACID; TRIFLUOROMETHANESULFONIC ACID TRIMETHYLSILYL ESTER; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; GLYCOSYLATION; HIGH TEMPERATURE; LOW TEMPERATURE; NUCLEOPHILICITY; PRIORITY JOURNAL;

BORANES; CATALYSIS; GLYCOSIDES; GLYCOSYLATION; IMIDOESTERS; MESYLATES; OXYGEN; PHENOLS; TRIMETHYLSILYL COMPOUNDS;

EID: 84867781665     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2012.09.025     Document Type: Article

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