Stereochemical features of Lewis acid-promoted glycosidations involving 4′-spiroannulated DNA building blocks

Journal of Organic Chemistry

Volumn 69, Issue 22, 2004, Pages 7442-7447

  Paquette, Leo A ^a   Seekamp, Christopher K ^a,b   Kahane, Alexandra L ^a,c   Hilmey, David G ^a   Gallucci, Judith ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b The Institute for Diabetes Discovery   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; CATALYSIS; DNA; X RAY CRYSTALLOGRAPHY;

COUPLING REACTIONS; LEWIS ACID;

STEREOCHEMISTRY;

ACETONITRILE; ALPHA SPIRONUCLEOSIDE; DICHLOROMETHANE; DNA; LEWIS ACID; NUCLEIC ACID BASE; NUCLEOSIDE DERIVATIVE; SILANE DERIVATIVE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CHEMICAL REACTION KINETICS; DIHYDROXYLATION; ENANTIOMER; GLYCOSIDATION; MOLECULAR MECHANICS; NUCLEAR OVERHAUSER EFFECT; STEREOCHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

4-BUTYROLACTONE; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; DNA; GLYCOSIDES; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR MIMICRY; MOLECULAR STRUCTURE; SPIRO COMPOUNDS; STEREOISOMERISM; TIN COMPOUNDS;

EID: 6344219873     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048904g     Document Type: Article

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