Endo-5-bromo-1,2,3,4,5,6-hexamethylbicyclo[2.1.1]hexenyl cation.
✍ Scribed by H. Hogeveen; P.W. Kwant
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 205 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Per-on Preen.
📜 SIMILAR VOLUMES
The non-classical 1,2,3,4,5,6-hexsmethylbicyclo C2.1.11 hexenyl cations (la), (lb) were shown to react with nucleophlles at carbon atoms 2 and 3 as well as at carbon atom 6. The
The title compound, C 29 H 24 Br 2 , has crystallographic twofold rotation symmetry. The Br atom in the 2 position is disordered with the methyl group in the 6 position. The biphenyl bridge bond distance and the torsion angle between the rings are in good agreement with similar previously reported s
## A brief synthesis of endo-2-bromo-5-thiabicyclo [2.1 .I]hexane (9) has been developed involving conversion of 3-cyclopentenol (6) to 3-thioacetoxycyclopentene (7), bromination of this giving trans-l,2-di- bromo-4-thioacetoxycyclopentane (8), and treatment of the latter with base. Compound 9 is