Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Stereochemistry in Oxidation of Allylic Alcohols by Cell-free System of Callus induced from Cannabis sativa L.
KOICHI TAKEYAHIDEJI ITOKAWA
Author information
Keywords: alcohol oxidase
JOURNAL FREE ACCESS

1977 Volume 25 Issue 8 Pages 1947-1951

Details
Abstract
In the cell-free system of callus induced from Cannabis sativa L. (Moraceae), the pro-R hydrogen from C-1 methylene of primary allylic alcohols such as trans-cinnamyl alcohol and geraniol was abstracted. In an example of secondary allylic alcohols biotransformations, S-(-)-isophorol of the racemate was biotransformed to isophorone, and (+)-trans-verbenol of four isomers, such as (+)-and (-)-trans-verbenol, and (+)-and (-)-cis-verbenol, was preferentially biotransformed to (+)-verbenone. We reported previously that the enzyme which catalyzed the oxidation of these allylic alcohols in the cell-free system of Cannabis callus was an alcohol oxidase.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top