Compared behavior of 5-deoxy-5-iodo-D-xylo- and L-arabinofuranosides in the reductive elimination reaction: A strong dependence on structural parameters and on the presence of Zn2+. A combined experimental and theoretical investigation

Journal of Organic Chemistry

Volumn 72, Issue 7, 2007, Pages 2271-2278

  Henon, Eric ^a   Bercier, Ariane ^a   Plantier Royon, Richard ^a   Harakat, Dominique ^a   Portella, Charles ^a  

^a UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATES; COMPLEXATION; MOLECULAR STRUCTURE; ORGANOMETALLICS; ZINC;

HOMOLYTIC RUPTURE; ORGANOZINC; RING OXYGEN ATOMS;

REACTION KINETICS;

5 DEOXY 5 IODO DEXTRO XYLOFURANOSIDE; 5 DEOXY 5 IODO LEVO ARABINOFURANOSIDE; ARABINOSE; CARBON; FURAN DERIVATIVE; HEMICELLULOSE; IODINE; MONOSACCHARIDE; ORGANOMETALLIC COMPOUND; OXYGEN; PYRANOSIDE; SOLVENT; UNCLASSIFIED DRUG; WATER; XYLOSE; ZINC ION;

ARTICLE; CHEMICAL BOND; CHEMICAL STRUCTURE; ELIMINATION REACTION; PARAMETER; REDUCTION; REDUCTIVE ELIMINATION;

EID: 84962463250     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0614590     Document Type: Article

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