Incorporation of a S-glycosidic linkage into a glyconucleoside changes the conformational preference of both furanose sugars

Carbohydrate Research

Volumn 342, Issue 1, 2007, Pages 16-22

  Buckingham, Joanne ^a   Brazier, John A ^a   Fisher, Julie ^b   Cosstick, Richard ^a  

^a UNIVERSITY OF LIVERPOOL   (United Kingdom)

^b UNIVERSITY OF LEEDS   (United Kingdom)

Author keywords

Conformational analysis; Glyconucleosides; Modified nucleoside; NMR; Thioglycoside

Indexed keywords

CHEMICAL BONDS; CONDENSATION; CONFORMATIONS; NITROGEN COMPOUNDS; NUCLEAR MAGNETIC RESONANCE;

DEOXY RIBOSE SUGARS; GLYCONUCLEOSIDES; NUCLEOSIDES; RIBOSE SUGARS; THIOGLYCOSIDE;

SUGARS;

1 (3 BETA DEXTRO RIBOFURANOSYL 2,3 DIDEOXY 3 THIO BETA DEXTRO RIBOFURANOSYL)THYMINE; 3' THIOTHYMIDINE; CARBOHYDRATE; DISACCHARIDE; GLYCONUCLEOSIDE; NUCLEOSIDE DERIVATIVE; RIBOSE; THIOGLYCOSIDE;

ARTICLE; CARBOHYDRATE SYNTHESIS; CONFORMATION; NUCLEAR MAGNETIC RESONANCE; POLYMERIZATION; PRIORITY JOURNAL;

CARBOHYDRATE CONFORMATION; DEOXY SUGARS; DISACCHARIDES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; RIBOSE; THIOGLYCOSIDES;

EID: 33845472888     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2006.11.007     Document Type: Article

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