Iodine-sodium cyanoborohydride-mediated reductive ring opening of 4,6-O-benzylidene acetals of hexopyranosides

Carbohydrate Research

Volumn 345, Issue 18, 2010, Pages 2709-2713

  Rao, Kaki Venkata ^a   Patil, Premanand R ^a   Atmakuri, Sridhar ^a   Kartha, K P Ravindranathan ^a  

^a NATIONAL INSTITUTE OF PHARMACEUTICAL EDUCATION AND RESEARCH NIPER   (India)

Author keywords

Benzylidene acetals; Iodine; Reductive ring opening; Regiospecific reactions

Indexed keywords

BENZYL ETHERS; BENZYLIDENE ACETALS; GLUCOSAMINES; MOLECULAR IODINE; MONO- AND DISACCHARIDES; PROTECTING GROUP; REGIOSPECIFIC; RING OPENING; SODIUM CYANOBOROHYDRIDE;

ESTERS; ETHERS; IODINE; SODIUM; SUGARS;

INDUSTRIAL CHEMICALS;

ACETAL; CYANOBOROHYDRIDE SODIUM; DISACCHARIDE; ETHER; GLUCOSAMINE; GLYCOSIDE; IODINE; MONOSACCHARIDE; NITRILE; PYRAN DERIVATIVE; SODIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; PRIORITY JOURNAL; REDUCTION; RING OPENING;

BENZYLIDENE COMPOUNDS; BOROHYDRIDES; IODINE; MOLECULAR STRUCTURE;

EID: 78649328278     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2010.10.013     Document Type: Article

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