Author:
Anastasiou D,Campi EM,Fallon GD,Jackson WR
Abstract
Reexamination of the 1H and 13C n.m.r. spectra of the supposed 4,5-dihydro-3H-1-benzazepin-5-ols (1) has led to a reassignment of their structure as 2,3,4,5-tetrahydro-2,5-epoxy-1H-1-benzazepines (3) and the new structure has been confirmed by a single-crystal X-ray structure determination of the 5-phenyl derivative (3; R1 = H, R2 = Ph). Similar examination of the n.m.r. spectra of the supposed 3,4,5,6-tetrahydro-1,6-benzodiazocines (2) has led to their reassignment as the pyrrolo [1,2-a] benzimidazoles (4).
Cited by
8 articles.
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1. Synthesis and antimicrobial activity of some new 4H-pyrrolo[1,2-a]benzimidazoles;Chemical Research in Chinese Universities;2014-09-15
2. ChemInform Abstract: Reassignment of the Compounds Reported to be 4,5-Dihydro-3H-1- benzazepin-5-ols as 2,3,4,5-Tetrahydro-2,5-epoxy-1H-1-benzazepines and 3,4,5,6-Tetrahydro-1,6-benzodiazocines as 2,3,3a,4-Tetrahydro-1H- pyrrolo(1,2-a)benzimidazoles.;ChemInform;2010-08-19
3. Rhodium catalyzed hydroformylation of linalool;Applied Catalysis A: General;2006-08
4. High catalytic activity of RhCl3, 3H2O in HC(OEt)3 for the hydroformylation of alkenes: effect of P(OPh)3 on the selectivity;Catalysis Communications;2003-12
5. Synthesis of Medium and Large Cyclic Amines in Rhodium-Catalysed Reactions of Aminoalkenes with H2/CO;Australian Journal of Chemistry;2000