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Synthesis and reactivity of exo- and endo-5-5substituted bicyclo[2.1.0]pentanes

✍ Scribed by J.J. Tufariello; A.C. Bayer; J.J. Spadaro Jr.


Book ID
108383300
Publisher
Elsevier Science
Year
1972
Tongue
French
Weight
211 KB
Volume
13
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


Thermal behavior of exo-5-substituted bi
✍ J.J. Tufariello; A.C. Bayer πŸ“‚ Article πŸ“… 1972 πŸ› Elsevier Science 🌐 French βš– 202 KB

Recent investigations of the solvolytic behavior of s-5-bicyclo[2.1.0]pentyl derivatives (I) have uncovered a remarkable reactivity (1). Thus,

Solvolyse von exo-bicyclo-[2,1,0]-pentyl
✍ Klaus Fellenbergger; Ulrich SchΓΆllkopf πŸ“‚ Article πŸ“… 1972 πŸ› Elsevier Science 🌐 French βš– 201 KB

Wle friiher berlchtet 1,2) nlmmt die Solvolysegeschwlndlgkelt von exo-Blcyclo-(n, l,O)-alkyltosylaten (I) In der Folge n = 5.4.3 ab, wobel der Effekt helm Ubergang von n = 4 nach n = 3 besonders ausgeprlgt 1st (vgl. Tab. 1). Dies 1st ver-st&ndllch, well die mit der Ionlsatlon verbundene Dlsrotatlon

On the acetolysis of /exo - and /endo-bi
✍ Kenneth B. Wiberg; Richard Fenoglio πŸ“‚ Article πŸ“… 1963 πŸ› Elsevier Science 🌐 French βš– 127 KB

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