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Rearrangement of the trans-Tricyclo[4.2.0.01,3]oct-4-enyl Skeleton

✍ Scribed by Elena S. Koltun; Steven R. Kass

Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
145 KB
Volume
56
Category
Article
ISSN
0040-4020

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✦ Synopsis

AbstractÐThe acetolysis of a tosylate with a novel tricyclic skeleton was examined. Two major products (a tosylate and an acetate) are formed and both are the result of a skeletal rearrangement. A mechanism to account for the observed products is proposed and preliminary kinetic data are reported.

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