1985
DOI: 10.1107/s0108270185007326
|View full text |Cite
|
Sign up to set email alerts
|

4-Phenyl-6,7,8,9-tetrahydro-1H-2,3-benzodiazepine 2-oxide, C15H16N2O

Abstract: (2) and 1.268 (2) A respectively. The boat conformation adopted by most 1,2-diazepine rings is unperturbed by the oxide ligand which serves to weaken the N=N double bond and lowers the activation energy for ring inversion.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1996
1996
2005
2005

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 1 publication
0
1
0
Order By: Relevance
“…The central seven-membered diazepinthione ring (atoms C4/C5/C7-C9/N1/N2) adopts a boat conformation. The boat conformation is predominantly observed for the seven-membered ring of benzodiazepine and its derivatives, even with different double-bond positions and widely differing substituents (Walkinshaw, 1985;Torres et al, 2005). The internal torsion angles of the ring are shown in Fig.…”
Section: Commentmentioning
confidence: 99%
“…The central seven-membered diazepinthione ring (atoms C4/C5/C7-C9/N1/N2) adopts a boat conformation. The boat conformation is predominantly observed for the seven-membered ring of benzodiazepine and its derivatives, even with different double-bond positions and widely differing substituents (Walkinshaw, 1985;Torres et al, 2005). The internal torsion angles of the ring are shown in Fig.…”
Section: Commentmentioning
confidence: 99%