Oxidative Cyclization of Linalol by Various Microorganisms

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概要

• 論文の詳細を見る

• (±) Linalol is cyclized into cis and trans linalol oxides by various microorganisms. This reaction, assuming an intermediate epoxidation step, is analogous to the corresponding step proposed for the biosynthesis of ionophorous antibiotics.

• 社団法人 日本農芸化学会の論文

著者

• DAVID Lucien

  Laboratoire de Chimie Organique Biologique

• VESCHAMBRE Henri

  Laboratoire de Chimie Organique Biologique

• VESCHAMBRE Henri

  Laboratoire de Chimie Organique Biologique, E.R.A. 392 du CNRS, Université de Clermont-II

• DAVID Lucien

  Laboratoire de Chimie Organique Biologique, E.R.A. 392 du CNRS, Université de Clermont-II

関連論文

• Nigericic Acids, Two New Chemical Derivatives of Nigericin(Organic Chemistry)
• Effects of Exogenous Methyl Oleate on the Biosynthesis of Nigericin, a Polyether Carboxylic Antibiotic, by Streptomyces hygroscopicus NRRL B-1865
• Reduction of α, β-Unsaturated Carbonyl Compounds by Some Actinomycetes
• Reduction of α, β-Unsaturated Ketones with Tetrahymena pyriformis-A Detoxication Reaction
• Oxidative Cyclization of Linalol by Various Microorganisms

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