Selected 1,4-and 1,5-benzoheterazepinones, prepared by the Schmidt rearrangement of flavanone analogues, were converted to the corresponding thiolactam derivatives using phosphorus pentasulfide. The proton and carbon chemical shifts of the thiolactam derivatives are compared with those of their lact
1H and 13C NMR identification of unexpected 3,4-dihydroquinoxalines in the syntheses of 1,5-benzodiazepine derivatives
✍ Scribed by E. M. Tjiou; E. G. Lhoussaine; D. Virieux; A. Fruchier
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 141 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1593
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✦ Synopsis
Abstract
The reaction between o‐phenylenediamines, dehydroacetic acid and aromatic aldehydes is shown to give not only the expected 1,5‐benzodiazepine derivative but also a 3,4‐dihydroquinoxaline, the structure of which was determined by its ^1^H and ^13^C 1D and 2D NMR spectra. Copyright © 2005 John Wiley & Sons, Ltd.
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