Author:
Everest DJ,Grant PK,Slim GC,Yeo IKL
Abstract
Following the ozonolysis of a series of allylic hydroxy olefins derived from manool (6) we propose a mechanism which accounts for the anomalous ozonolysis products of allylic hydroxyl compounds in nucleophilic and non- nucleophilic solvents. It involves intramolecular participation by the allylic hydroxyl to form a hydroperoxy epoxide rather than the 1,2- nucleophilic migration from carbon to oxygen as proposed in the Criegee rearrangement mechanism.
Cited by
14 articles.
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