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Stereochemical factors in the epoxidation of substituted cyclohexenes

โœ Scribed by Patrick M. McCurry Jr.


Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
129 KB
Volume
12
Category
Article
ISSN
0040-4039

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## Abstract Racemic __trans__โ€anethole epoxide [1โ€(4โ€ฒโ€methoxyphenyl)โ€propaneโ€1,2โ€oxide] was incubated with water, buffers, and rat liver microsomes and cytosol and the stereochemistry of the diols produced was determined by HPLC as their dicamphanyl esters. The diol metabolites were isolated by HPL