Unique tandem Heck-lactamization naphthyridinone ring formation between acrylanilides and halogenated pyridines.

Abstract

The Heck coupling of acrylanilides with 4-bromo-2-chloro-3-iodo-pyridine using palladium acetate can produce bis-Heck products or undergo an unusual tandem Heck-lactamization ring formation to generate 5-chloro-1-aryl-1,6-naphthyridin-2(1H)-ones. 

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