Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 1997; 1997(3): 297-300
DOI: 10.1055/s-1997-1176
DOI: 10.1055/s-1997-1176
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Preparation of Spiro[1-benzazepine-4,1'-cyclohexane] Derivatives from 1H-1-Benzazepine-2,5(3H,4H)-diones and Mannich Bases
Further Information
Publication History
Publication Date:
31 December 2000 (online)
3'-Aroyl-4'-aryl-4'-hydroxyspirol[1-benzazepine-4,1'-cyclohexane]-2,5(1H,3H)-diones were synthesized by reaction of 1H-benzazepine-2,5(3H,4H)-diones with aromatic ketone Mannich bases. The new compounds exhibited in vitro antitumor activity on distinct cell lines.
tandem Michael-aldol reaction - 1-benzazepine-2,5-diones - Mannich bases - cyclohexanols - spiro compounds