Stereochemistry of the cleavage of the 10-hydroperoxide isomer of linoleic acid to 1-octen-3-ol by a hydroperoxide lyase from mushrooms (psalliota bispora)-Reference-Cited by-同舟云学术

Stereochemistry of the cleavage of the 10-hydroperoxide isomer of linoleic acid to 1-octen-3-ol by a hydroperoxide lyase from mushrooms (psalliota bispora)

Published:1984-08 Issue:1 Volume:795 Page:163-165
ISSN:0005-2760
Container-title:Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism

Author:

Wurzenberger Margot,Grosch Werner

Publisher

Elsevier BV

Subject

Endocrinology,Biochemistry,Biophysics

Reference8 articles.

1. The formation of 1-octen-3-ol from the 10-hydroperoxide isomer of linoleic acid by a hydroperoxide lyase in mushrooms (Psalliota bispora)

2. The Steady-State Kinetics of the Oxygenation of Linoleic Acid Catalysed by Soybean Lipoxygenase

3. Specificity of flaxseed lipoxidase

4. Esterification of Fatty Acids with Diazomethane on a Small Scale

5. Determination by capillary gas-liquid chromatography of the absolute configurations of unsaturated fatty acid hydroperoxides formed by lipoxygenases

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