Conformational analysis of benzoanellated nine-membered rings, Part 1. 1,4,5,7-tetrahydro-3H-2,6-benzodithionin derivatives
✍ Scribed by Barbara Rys; Helmut Duddeck; Monika Hiegemann
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 450 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
The NW? spectra of compounds l-5, recorded at different temperatures, are discussed and interpreted in terms of conformational eguilibrium. Ground state conformations are found to be chiral, ring inversion barriers are surprisingly high (ca 48 kJ/mol).
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## Abstract Temperature‐dependent ^1^H‐ and ^13^C‐NMR spectra of the title compound are presented. Coalescence effects are discussed and assigned to two dynamic processes: (a) ring inversion of the nine‐membered ring, (b) racemization of the enantiomeric ground‐state conformations of the nine‐membe
## Abstract Temperature‐dependent ^1^H and ^13^C NMR spectra of the title compounds are presented. The coalescence effects in the spectra are discussed and assigned to the racemization of the __C__~2~ symmetry conformation of the nine‐membered ring. The barrier of this process is __ca__. 64 kJ mol^
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
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