Highly stereoselective β-anomeric glycosidation of a 2′-deoxy syn-5′-configured 4′-spironucleoside

Journal of Organic Chemistry

Volumn 71, Issue 4, 2006, Pages 1647-1652

  Dong, Shuzhi ^a   Paquette, Leo A ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANOMER; DIHYDROXY LACTONE; GLYCOSIDATION; SPIRONUCLEOSIDE;

MONOMERS; REACTION KINETICS;

NUCLEIC ACIDS;

4' SPIRONUCLEOSIDE; LACTONE DERIVATIVE; NUCLEOSIDE DERIVATIVE; SILOXANE; SPIRO COMPOUND; THYMINE; UNCLASSIFIED DRUG;

ARTICLE; DEIODINATION; DEPROTECTION REACTION; DESILYLATION; ENANTIOMER; GLYCOSIDATION; RING OPENING; STEREOCHEMISTRY;

GLYCOSYLATION; LACTONES; NUCLEOSIDES; SPIRO COMPOUNDS; STEREOISOMERISM; THYMINE;

EID: 33644531539     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052324h     Document Type: Article

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