## Abstract 1,2 __exo__βDiiodoβnorbornane (**4**) was prepared from norcamphor hydrazone by oxidative iodination and subsequent rearrangement of the 2,2βdiiodoβbicyclo [2.2.1]heptane (**2**). The stable Ξ±βiodohydrazone **11** was obtained from 1βiodoβbicyclo[2.2.1]heptanβ2βone (**10**), which itsel
β¦ LIBER β¦
Preparation of enantiomerically pure 3-endo-sulfonylmethyl substituted bicyclo[2.2.1]heptane-2-endo-carboxylic acids
β Scribed by P. Metz
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 445 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0040-4020
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endo-Bicyclo[2.2.2] oct-5-ene-2-carboxylic acid, in acidic solution, cyclizes to give a mixture of three isomeric lactones. These three isomers have different stabilities and are partly interconvertible, but their simultaneous decomposition makes the experimental study of these equilibria difficult