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Synthesis 2011(4): 669-673
DOI: 10.1055/s-0030-1258416
DOI: 10.1055/s-0030-1258416
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Ring-Closing Metathesis Approach to 2H-2-Benzazepine-1,3-diones
Further Information
Received
1 December 2010
Publication Date:
19 January 2011 (online)
Publication History
Publication Date:
19 January 2011 (online)
![](https://www.thieme-connect.de/media/synthesis/201104/lookinside/thumbnails/10.1055-s-0030-1258416-1.jpg)
Abstract
A series of diversely substituted 2H-2-benzazepine-1,3-diones were efficiently prepared from the unsaturated precursors, N-acyl-o-vinylbenzamides, through a ring-closing metathesis reaction. The parent compounds were easily obtained from the appropriate o-vinylbenzoic acids.
Key words
fused-ring systems - acylation - ring closure - metathesis - imides
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