Use of acyl substituents to favour 2,3-epoxidation of 5,7-dioxygenated flavones with dimethyldioxirane

Tetrahedron

Volumn 67, Issue 4, 2011, Pages 718-726

  Compton, Benjamin J ^a   Larsen, Lesley ^a   Weavers, Rex T ^a  

^a UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

Acylation; Dimethyldioxirane; Epoxidation; Flavone

Indexed keywords

3 HYDROXY 5 ACETOXY 7 METHOXYFLAVONE; 3 HYDROXY 7 ACETOXY 5 METHOXYFLAVONE; 5 BENZOYLOXY 3 HYDROXY 7 METHOXYFLAVONE; 5 BENZOYLOXY 7 BENZYLOXY 3 HYDROXYFLAVONE; 5,7 DIACETOXY 3 HYDROXYFLAVONE; 5,7 DIBENZOYLOXY 3 HYDROXYFLAVONE; 5,7 DIMETHOXY 3 HYDROXYFLAVONE; 7 BENZOYLOXY 3 HYDROXY 5 METHOXYFLAVONE; DIMETHYLDIOXIRANE; EPOXIDE; FLAVONE DERIVATIVE; FLAVONOL DERIVATIVE; NUCLEOPHILE; TOLUENESULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; DEMETHYLATION; DENSITY FUNCTIONAL THEORY; EPOXIDATION; IONIZATION; PRIORITY JOURNAL; SUBSTITUTION REACTION; SYNTHESIS;

EID: 78650585018     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.11.076     Document Type: Article

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