Chemistry Letters
New application of 1, 4-dihydropyridine system: Michael reactions mediated by 1, 4-dihydropyridine-enolate adduct in micellar medium
SH Mashraqui, MA Karnik
Index: Mashraqui, Sabir H.; Karnik, Madhavi A. Chemistry Letters, 2003 , vol. 32, # 11 p. 1064 - 1065
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Citation Number: 1
Abstract
1, 4-dihydropyridine-acetophenone enolate adduct, in catalytic amount effects Michael reactions in aqueous cationic micelles of cetyltrimethylammonium bromide. The enolate, generated by dissociation of the adduct abstracts a proton from readily enolizable substrates to bring about the Michael reaction under mild conditions in fair to good yields without side products.
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