Convenient enantiopure synthesis of (2S,3R)-2-O-benzyl-3,4-O- isopropylidene-D-erythritol from D-(+)-glucono-δ-lactone: A potential C4 chiral building block

Synthesis

Volumn , Issue 13, 2005, Pages 2267-2269

  Vijayasaradhi, Sivalenka ^a   Beedimane, Manjunath Narayana ^a   Aidhen, Indrapal Singh ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY MADRAS   (India)

Author keywords

Eliminations; Lactones; Ozonolysis; Reduction

Indexed keywords

OZONE; REDUCTION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

ELIMINATIONS; LACTONES; OZONOLYSIS; TARGET COMPOUND;

ORGANIC COMPOUNDS;

2 O BENZYL 3,4 O ISOPROPYLIDENE DEXTRO ERYTHRITOL; DEXTRO GLUCONO ALPHA LACTONE; ERYTHRITOL; LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ELIMINATION REACTION; ENANTIOMER; ENANTIOSELECTIVITY; OZONOLYSIS; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 23944458204     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-869986     Document Type: Article

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