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Stereochemical aspects of the hydration of trans-anethole epoxide in the rat

✍ Scribed by Takashi Ishida; Stephen V. J. Bounds; Professor John Caldwell

Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
389 KB
Volume
7
Category
Article
ISSN
0899-0042

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✦ Synopsis

Abstract

Racemic trans‐anethole epoxide [1‐(4′‐methoxyphenyl)‐propane‐1,2‐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 HPLC from the urine of rats administered [1′‐^14^C] trans‐anethole and their stereochemistry determined after derivatization to their camphanyl esters. The stereochemical course of the metabolism of trans‐anethole by rat liver microsomes and cytosol is discussed. © 1995 Wiley‐Liss, Inc.

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