The Mechanism of the Double Bond Cleavage in the Titanium Zeolite‐catalyzed Oxidation of α‐Methylstyrene by Hydrogen Peroxide: the β‐Hydroperoxy Alcohol as Intermediate — Waldemar Adam (1996) | RDL Network
The Mechanism of the Double Bond Cleavage in the Titanium Zeolite‐catalyzed Oxidation of α‐Methylstyrene by Hydrogen Peroxide: the β‐Hydroperoxy Alcohol as Intermediate
It is unequivocally shown that acetophenone, an oxidation product in the titanium zeolite‐catalyzed oxidation of α‐methylstyrene, derives from 2‐hydroperoxy‐2‐phenyl‐1‐propanol as intermediate, which was detected and isolated in this reaction for the first time.
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