Stereochemistry of the yeast - mediated conversion of delta 2 - decenolide into delta decanolide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Microbial production of natural δ-decalactone and δ-dodecalactone from the corresponding α,β-unsaturated lactones in Massoi bark oil
2. Stereochemistry of the methyne–methylene conversion in the biogeneration of (S)-δ-decanolide and (S)-γ-dodecanolide from (13RS)-13-hydroxyoctadeca-9Z,11E-dienoic and (10RS)-10-hydroxyoctadec-8E-enoic acid
3. On the mode of conversion of racemic C14-C19 .gamma.-hydroxy alkene fatty acids into C7-C11, optically active .gamma. and .delta.-lactones in Cladosporium suaveolens
4. Stereochemical course of the reduction of cinnamaldehyde and cinnamyl alcohol to 3-phenylpropanol by fermenting Baker's yeast
5. Biosynthesis of ansatirenin: stereochemical course of the final reduction step leading to the cyclohexanecarboxylic acid moiety
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1. Applications of biocatalytic C C bond reductions in the synthesis of flavours and fragrances;Journal of Biotechnology;2024-07
2. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie International Edition;2023-02-27
3. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie;2023-02-27
4. Ene-reductase transformation of massoia lactone to δ-decalactone in a continuous-flow reactor;Scientific Reports;2021-09-22
5. Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers;ACS Catalysis;2020-10-26
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