On the acetolysis of /exo - and /endo-bicyclo[2.1.1] - hexyl-5 tosylates
β Scribed by Kenneth B. Wiberg; Richard Fenoglio
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 127 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Although good evidence has been found for ancbimerlc rmsistaace in the solvolytic reactions of unsaturated systems such as the 2-norbornen-~1 tosylates be,,/ kendo = 8 X 10')' and the 'I-isopropylidene 5-norbornen-2-yl tosylates', the smaller rate factor observed with saturated l ystomb such as the 2-norbornyl tosylates(ksxo/ kendo = 350)' lends an element of uncertainty in the interpretation of the results.' We have observed that the bicyclo[ 2. 1. lbexyl-5 tosylatteas
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π SIMILAR VOLUMES
## 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