A straightforward α-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl α-T-antigen

Carbohydrate Research

Volumn 344, Issue 4, 2009, Pages 432-438

  Chang, Shih Sheng ^a   Lin, Chun Cheng ^b   Li, Yaw Kuen ^a   Mong, Kwok Kong Tony ^a  

^a NATIONAL CHIAO TUNG UNIVERSITY   (Taiwan)

^b NATIONAL TSING HUA UNIVERSITY   (Taiwan)

Author keywords

T Antigen; Aromatic; Glycosylation; Imidate; Stereoselective

Indexed keywords

AROMATIC; IMIDATE; IMIDATES; STEREO-SELECTIVE SYNTHESIS; STEREOSELECTIVE; STEREOSPECIFIC SYNTHESIS; SYNTHETIC UTILITIES; TRICHLOROACETIMIDATES;

ANTIGENS; ESTERIFICATION; GLYCOSYLATION; STEREOCHEMISTRY; STEREOSELECTIVITY;

AROMATIC COMPOUNDS;

4 METHYLUMBELLIFERYL ALPHA T ANTIGEN; TUMOR ANTIGEN; UNCLASSIFIED DRUG;

ARTICLE; CARBOHYDRATE SYNTHESIS; GLYCOSYLATION; PRIORITY JOURNAL; STEREOSPECIFICITY;

ANTIGENS, VIRAL, TUMOR; CARBOHYDRATE CONFORMATION; CARBOHYDRATE SEQUENCE; GLYCOPEPTIDES; GLYCOSYLATION; IMIDOESTERS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; STEREOISOMERISM; TRICHLOROACETIC ACID;

EID: 61349148628     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2008.12.013     Document Type: Article

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