Chromanones 2 -hydroxychalcones

A comparison of the polarographic reduction of 2- and 3-substituted thiophenes have shown that the 2-isomers are more easily reduced than the 3-isomers. Polarography has also been used for the quantitative study of the dehalogenative reduction of 2-halo-5-carbonyl thiophenes and for the study of the hydroxychalcone-chromanone equilibrium in thienylsubstituted compounds. ... 

The mechanisms of the cyclisation of 2 -hydroxychalcone derivatives which can lead to flavanones, flavones and aurones have been reviewed <95MI1> and the formation of 3-hydroxy- chromanones and -flavanones from l-(2-hydroxyphenyl)-2-propen-l-ones via the epoxide has been optimised <96JOC5375>. 

Another example of an equilibrium involving ring-formation is the cyclization of 2-hydroxychalcones (12) to form chromanones (8 b). The... 

Disubstituted flavanones and chromanones are produced with good enantioselectivity from chalcones activated by an a-fert-butyl ester function through an intramolecular Michael addition catalysed by a chiral thiourea derivative. In situ decarboxylation enhances the ee and yields remain high <07JA3830>. A comprehensive study of the asymmetric cyclisation of 2 -hydroxychalcones to flavanones has refuted the ability of camphorsulfonic acid to achieve enantioselectivity but has shown that cinchona-based catalysts can be effective <07EJO5886>. 

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