Empirical force field calculations XXI. The ring inversion of cis-transoid-cis-1,4,4a,5,8,8a,9,9a,10,10a-decahydroanthracene
✍ Scribed by D. Tavernier; J. M. A. Baas; B. van de Graa; P. Vanhee
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 356 KB
- Volume
- 102
- Category
- Article
- ISSN
- 0165-0513
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
4 4 . 7 kJ mol-1 ( K = 0 . 5 ) . hydrocarbon. This increase is rationalized by a perturbational force field study. The reliability of the perturbational calculation was tested by a comparison of calculated and experimental conformational equilibria in various 1and 2-oxygenated \*-decalins. The Gibb
The title diadduct, C 16 H 16 O 2 , has been redetermined by X-ray diffraction methods at 120 K. In this work, we report more exact values of bond and angles.
The regiosomeric quinones 5-acetyloxymethyl-4,4,8-trimethyl-( ) and 8-acetyloxymethyl-4,4,5trimethylanthracene-1,9,10(4H)-trione (6) were synthesized and their regiochemistry was assigned on the basis of the unambiguous structure elucidation of 9,10-dihydroxy-5-acetyloxymethyl-4,4,8-trimethyl-5,8-di