Rearrangement of an N-aryl-2-vinyltetrahydro-4-oxoquinoline to an acridine derivative
Heterocycles(1998)
Abstract
Acridine (4) has been obtained by acidic rearrangement of N-aryl-2-vinyltetrahydro-4-oxoquinoline (2). The mechanism involved a retro-Michael process followed by the attack of the electron rich aromatic ring onto the keto group.
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Key words
acridine derivative,rearrangement,n-aryl
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