A convenient approach for access to both carbapentofuranoses and carbahexopyranoses. Stereocontrolled synthesis of enantiopure Carba-D-ribofuranoses, Carba-D-arabinofuranoses and Carba-L-gulopyranose

Journal of Organic Chemistry

Volumn 71, Issue 26, 2006, Pages 9687-9694

  Ghosh, Subrata ^a   Bhaumik, Tanurima ^a   Sarkar, Niladri ^a   Nayek, Abhijit ^a  

^a DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CARBASUGARS; HYDROXYL GROUPS; HYDROXYMETHYL GROUPS; METATHESIS;

ALCOHOLS; ANTIBIOTICS; DERIVATIVES; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

SUGARS;

ACETAL; ANTIBIOTIC AGENT; ARISTEROMYCIN; CARBA DEXTRO ARABINOFURANOSE; CARBA DEXTRO RIBOFURANOSE; CARBA LEVO GULOPYRANOSE; CARBAHEXOPYRANOSE DERIVATIVE; CARBAPENTOFURANOSE DERIVATIVE; CYCLOALKENE; CYCLOHEXENOL; CYCLOPENTENOL; FUNCTIONAL GROUP; GLYCERALDEHYDE; HYDROXYL GROUP; METHYL GROUP; UNCLASSIFIED DRUG;

ARTICLE; BIOTRANSFORMATION; CARBOHYDRATE SYNTHESIS; CARBON NUCLEAR MAGNETIC RESONANCE; COMPLEX FORMATION; DIASTEREOISOMER; DIHYDROXYLATION; ENANTIOMER; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; REACTION ANALYSIS; REDUCTION; RING CLOSING METATHESIS; STEREOCHEMISTRY;

CYCLOHEXANOLS; CYCLOPENTANES; FURANS; MOLECULAR STRUCTURE; MONOSACCHARIDES; PYRANS; STEREOISOMERISM;

EID: 33845952182     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061717t     Document Type: Article

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