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On the acetolysis of /exo - and /endo-bicyclo[2.1.1] - hexyl-5 tosylates

✍ 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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✦ 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

(1)

(2)

(3) (4)

(5)


πŸ“œ SIMILAR VOLUMES


Preparation of 1,2exo- and 1,2endo-Diiod
✍ Hugo Camenzind; Ernst-Peter Krebs; Reinhart Keese πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 German βš– 399 KB

## Abstract 1,2 __exo__‐Diiodo‐norbornane (**4**) was prepared from norcamphor hydrazone by oxidative iodination and subsequent rearrangement of the 2,2‐diiodo‐bicyclo [2.2.1]heptane (**2**). The stable α‐iodohydrazone **11** was obtained from 1‐iodo‐bicyclo[2.2.1]heptan‐2‐one (**10**), which itsel