Rearrangement of an N-aryl-2-vinyltetrahydro-4-oxoquinoline to an acridine derivative

Heterocycles(1998)

Cited 2|Views1
No score
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.
More
Translated text
Key words
acridine derivative,rearrangement,n-aryl
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined