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

文献索引：Mashraqui, Sabir H.; Karnik, Madhavi A. Chemistry Letters, 2003 , vol. 32, # 11 p. 1064 - 1065

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被引用次数: 1

摘要

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.