Title: Highly diastereoselective Michael reaction under solvent-free conditions using microwaves: conjugate addition of flavanone to its chalcone precursor
Abstract: Microwave-assisted reaction of 2′-hydroxychalcones in the presence of DBU resulted in the formation of hitherto unknown dimers by conjugate addition of the intermediate cyclic ketone to the starting enone.
Publication Year: 2001
Publication Date: 2001-02-01
Language: en
Type: article
Indexed In: ['crossref']
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Cited By Count: 40
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