Glycosylation of α-amino acids by sugar acetate donors with InBr 3. Minimally competent Lewis acids

Carbohydrate Research

Volumn 351, Issue , 2012, Pages 121-125

  Lefever, Mark R ^a   Szab, Lajos Z ^a   Anglin, Bobbi ^a   Ferracane, Michael ^a   Hogan, Joanna ^a   Cooney, Lauren ^a   Polt, Robin ^a  

^a University of Arizona   (United States)

Author keywords

Glycosylation; Indium tribromide; O linked glycopeptides; Serine; Threonine

Indexed keywords

GLYCOPEPTIDE SYNTHESIS; INDIUM TRIBROMIDE; LEWIS ACID; O-LINKED; SERINE; SIDE PRODUCTS; SIMPLIFIED METHOD; SUGAR ACETATES; THREONINE;

AMINO ACIDS; ESTERIFICATION; GLYCOSYLATION; ORGANOMETALLICS; PEPTIDES;

SUGARS;

ACETIC ACID; AMINO ACID DERIVATIVE; GLYCOSIDE; INDIUM TRIBROMIDE; LEWIS ACID; N (9 FLUORENYLMETHOXYCARBONYL) LEVO SERINE GLYCOSIDE; N (9 FLUORENYLMETHOXYCARBONYL) LEVO THREONINE GLYCOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; GLYCOSYLATION; PRIORITY JOURNAL; SYNTHESIS;

ACETATES; AMINO ACIDS; CATALYSIS; GLYCOSYLATION; INDIUM; LEWIS ACIDS;

EID: 84858077232     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2012.01.008     Document Type: Article

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