Stereochemical Analysis of the Enzymic Reduction of the Double Bond of α- and β-Substituted Nitrostyrenes and α-Ethoxycinnamaldehyde through Deuterium Labelling Experiments-Reference-Cited by-同舟云学术

Stereochemical Analysis of the Enzymic Reduction of the Double Bond of α- and β-Substituted Nitrostyrenes and α-Ethoxycinnamaldehyde through Deuterium Labelling Experiments

Published:2010-07-26 Issue:26 Volume:2010 Page:5077-5084
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Brenna Elisabetta,Fronza Giovanni,Fuganti Claudio,Gatti Francesco G.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201000442/fullpdf

Reference26 articles.

1. Stereochemical course of the reduction of cinnamaldehyde and cinnamyl alcohol to 3-phenylpropanol by fermenting Baker's yeast

2. The mode of bakers' yeast transformation of 3-chloropropiophenone and related ketones. Synthesis of (2S)-[2-2H]propiophenone, (R)-fluoxetine, and (R)- and (S)-fenfluramine

3. Stereochemistry of the baker's yeast mediated reduction of the CC bond of (Z)- and (E)-5-benzoyloxyhex-3-en-2-one

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enzymatic strategies for asymmetric synthesis;RSC Chemical Biology;2021

2. Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers;ACS Catalysis;2020-10-26

3. Biocatalysis for synthesis of pharmaceuticals;Bioorganic & Medicinal Chemistry;2018-04

4. Asymmetric Bioreduction of β-Acylaminonitroalkenes: Easy Access to Chiral Building Blocks with Two Vicinal Nitrogen-Containing Functional Groups;ChemCatChem;2017-05-29

5. Biotransformation of 3-azidomethyl-4-phenyl-3-buten-2-one and analogs by Saccharomyces cerevisiae : New evidence for an S N 2′ mechanism;Tetrahedron: Asymmetry;2017-04