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Org Biomol Chem ; 10(15): 2946-9, 2012 Apr 21.
Article in English | MEDLINE | ID: mdl-22395456

ABSTRACT

Flavones were directly alkylated at the C-3 position in moderate yields using a xanthate-based oxidative radical addition procedure. This methodology is a suitable synthetic tool for the direct substitution of the vinylic and unactivated C-H bond of the C ring of the flavone by an alkyl functionality under neutral conditions.


Subject(s)
Alkylating Agents/chemistry , Flavones/chemical synthesis , Thiones/chemistry , Alkylation , Crystallography, X-Ray , Free Radicals/chemistry , Microwaves , Molecular Structure , Oxidation-Reduction
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