Diastereoselective epoxidation of oxazolidine-substituted alkenes by dimethyldioxirane and m-chloroperbenzoic acid: π-facial control through hydrogen bonding by the urea functionality

Organic Letters

Volumn 3, Issue 1, 2001, Pages 79-82

  Adam, Waldemar ^a   Schambony, Simon B ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

3 CHLOROPERBENZOIC ACID; 3-CHLOROPERBENZOIC ACID; ALKENE; AMINE; CHLOROBENZOIC ACID DERIVATIVE; DIMETHYLDIOXIRANE; EPOXIDE; OXAZOLE DERIVATIVE; OXAZOLIDINE; UREA;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; HYDROGEN BOND; METHYLATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION;

ALKENES; AMINES; CATALYSIS; CHLOROBENZOATES; EPOXY COMPOUNDS; HYDROGEN BONDING; MAGNETIC RESONANCE SPECTROSCOPY; METHYLATION; MOLECULAR STRUCTURE; OXAZOLES; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; UREA;

EID: 0035843282     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol006800w     Document Type: Article

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