Issue 8, 1988

Formation of acyclic α- and γ-ketols and 12-oxophytodienoic acid from linolenic acid 13-hydroperoxide by a flax enzyme preparation. Evidence for a single enzyme leading to a common allene epoxide intermediate

Abstract

Experiments with [14-2H2]linolenic acid confirm the requirement for a 13-hydroperoxide for 13-oxophytodienoic acid (12-oxoPDA) formation by a flax enzyme preparation; an allene epoxide intermediate is capable of explaining the formation of the acyclic α- and γ-ketols as well as 12-oxoPDA, suggesting the involvement of a single enzyme.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 558-560

Formation of acyclic α- and γ-ketols and 12-oxophytodienoic acid from linolenic acid 13-hydroperoxide by a flax enzyme preparation. Evidence for a single enzyme leading to a common allene epoxide intermediate

L. Crombie and D. O. Morgan, J. Chem. Soc., Chem. Commun., 1988, 558 DOI: 10.1039/C39880000558

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