## Abstract For Abstract see ChemInform Abstract in Full Text.
An x-ray study of the ring inversion in 1,3,4,5-tetrahydro-5-phenyl-2H-1,4-benzodiazepin-2-ones caused by carbamoylation
✍ Scribed by Mátyás Czugler; Alajos Kálmán; Julia Röhricht; Miklós Low; László Ürögdi; Lajos Kisfaludy
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 194 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
## Abstract DFT B3LYP calculation study was employed to estimate the regioselectivity of an electrophilic aromatic substitution in functionalized 2,3,4,5‐tetrahydro‐1,5‐benzodiazepin‐2(1__H__)‐ones. Charge density, frontier molecular orbital study, energetics of σ‐complex intermediates of electroph
## Abstract A route to optically active variously substituted 4‐methyl‐ and 4‐methyl‐7‐substituted 1,3,4,5‐tetrahydro‐2__H__‐1,5‐benzo‐diazepin‐2‐ones as analogues of commercially available Lofendazam (7‐chloro‐5‐phenyl‐1,3,4,5‐tetrahydro‐2__H__‐1,5‐benzodiazepin‐2‐one, 1) was developed. Fortyone v
## Abstract Two benzodiazepines, Diazepam and Flunitrazepam, labeled with carbon‐14 in position 5 of the diazepine ring have been synthesized. Use of a condensation between iminochlorides and ^14^C‐benzonitriles, followed by exhaustive methylation of the resulting quinazolines and hydrolyses is des