A novel conformational energy preference in 7-chloro-7-carboxamido-6b,7,8,8a-tetrahydrocyclobut[A]acenaphthylene
✍ Scribed by B.P. Plummer; M.P. Songster; W.H. Watson; A. Nagl
- Book ID
- 104204587
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 359 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
Ahset
The title compound (E-1) exhibits a conformational energy preference in which the carbonyl oxygen lies over the aromatic ring. This preferred conformation is shown to exist in the solid state by X-ray analysis of the crystal structure and in the solution phase by COSY studies of the NMR spectrum. Related compounds show no conformational preference in solution at room temperature on
📜 SIMILAR VOLUMES
The synthesis of conformationally locked analogs of epibatidine are described in which the key step is an intramolecular reductive palladium-catalyzed Heck-type coupling.
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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
In the title compound, C 28 H 32 Cl 2 N 6 O 6 , the dihedral angle between the two adjacent five-membered rings in the glycoluril unit is 70.18 (9) and molecules are connected mainly by C-HÁ Á ÁO intermolecular interactions.