## Abstract The ^1^H and ^13^C NMR spectra of 26 2,3‐dihydro‐[1,5]benzoxazepin‐4(5__H__)‐one derivatives and four thiono analogues are interpreted in terms of conformational equilibria. Similar to 1,3,4,5‐tetrahydro‐2__H__‐1,5‐benzodiazepin‐2‐ones, these compounds favour boat conformations of the s
Photoelectron spectra of Group 5 compounds. II. Conformational analysis of diphosphine (P2H4)
✍ Scribed by Elbel, Susanne.; Tom Dieck, Heindirk.; Becker, Gerd.; Ensslin, Walther.
- Book ID
- 127340829
- Publisher
- American Chemical Society
- Year
- 1976
- Tongue
- English
- Weight
- 469 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0020-1669
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An investigation of the molecular dynamics of substituted 1,3,4,5-tetrahydro-2H-l,Ibenzodiazepin-2-0ne derivatives revealed that these molecules adopt cycloheptadiene-like boat conformations. There is an equilibrium between the quasi-axial and the quasiequatorial conformer in which the quasi-axial c
## Abstract The conformational analysis of biologically active lofendazam (7‐chloro‐5‐phenyl‐1,3,4,5‐tetrahydro‐__2H__‐1,5‐benzodiazepin‐2‐one) is carried out by means of lanthanide shift reagent assisted ^1^H NMR spectroscopy: the lanthanide induced shift computer simulation suggests that in deute