47301-30-4Relevant academic research and scientific papers
Studies about the cyclization of 1,2-diamines with aldehydes and ketones
Lessel
, p. 649 - 653 (2007/10/02)
The reaction of the 1,2-dinucleophile ethylendiamine with benzaldehydes yields diimines, from o-phenylendiamine monoimines respectively benzimidazoles are formed. β-Diketones give 1,5-benzodiazepines. The different behaviour is explained by MNDO calculati
4-Benzoyl-5-phenyl-1,3-oxathiol-2-one. Synthesis and Reaction with N-Nucleophiles
He-Xi, Chang,Kollenz, Gert
, p. 501 - 504 (2007/10/02)
The synthesis of 4-benzoyl-5-phenyl-1,3-oxathiol-2-ones 1 and the behaviour of 1a against several amines were investigated to afford aminomercaptoethenes 2 or thiocarbamates 3, as well as complete cleavage to sulfur, dibenzoylmethane and the corresponding urea, depending on the nature of the N-nucleophile used.
