A new route to quinolone and indole skeletones via ketone- and ester-imide cyclodehydration reactions

Title
A new route to quinolone and indole skeletones via ketone- and ester-imide cyclodehydration reactions
Authors
김근철금교창
Issue Date
1997-01
Publisher
Heterocycles.
Citation
VOL 45, NO 10, 1979-1988
Abstract
Ketone-imide cyclodehydration reactions of aromatic succinimide and phthalimide (7, 8) have aforded quinolone acids (11, 12). Further transformation of the acids provided the corresponding esters (13, 14) and vinylogous urethanes (9, 10). Similarly, ester-imide cyclodehydration reactions of aromatic imide esters (19, 20) have afforded indole acids (23, 24).
URI
http://pubs.kist.re.kr/handle/201004/11971
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KIST Publication > Article
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