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Thermal and photochemical reactions of unsaturated bicyclic endoperoxides

✍ Scribed by Howard A.J. Carless; Robert Atkins; G.K. Fekarurhobo


Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
254 KB
Volume
26
Category
Article
ISSN
0040-4039

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✦ Synopsis


Thermal, and especially photochemical, rearrangement of the endoperoxides (1) and ( )-( ) gives By-epoxycycloalkanones as primary products, accompanied by the expected syn-diepoxides.

Unsaturated endoperoxides [e.g.(l)] are readily available by reaction of singlet oxygen ('0,) with conjugated dienes. 1 Such endoperoxides have proved extremely


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