1H and 13C NMR identification of unexpected 3,4-dihydroquinoxalines in the syntheses of 1,5-benzodiazepine derivatives.
E M Tjiou, E G Lhoussaine, D Virieux, A Fruchier
Index: Magn. Reson. Chem. 43(7) , 557-62, (2005)
Full Text: HTML
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 1H and 13C 1D and 2D NMR spectra.Copyright 2005 John Wiley & Sons, Ltd
Related Compounds
Related Articles:
2010-01-01
[Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho. Hokoku. (128) , 85-90, (2010)]
2012-01-01
[J. AOAC Int. 95(4) , 1069-73, (2012)]
2001-12-01
[Shokuhin Eiseigaku Zasshi 42(6) , 404-12, (2001)]
2007-06-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 67(2) , 564-7, (2007)]
2009-09-01
[J. Food Sci. 74(7) , M418-21, (2009)]