Biotransformation of 3-azidomethyl-4-phenyl-3-buten-2-one and analogs by Saccharomyces cerevisiae : New evidence for an S N 2′ mechanism-Reference-Cited by-同舟云学术

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Biotransformation of 3-azidomethyl-4-phenyl-3-buten-2-one and analogs by Saccharomyces cerevisiae : New evidence for an S N 2′ mechanism

Published:2017-04 Issue:4 Volume:28 Page:545-549
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

de Paula Bruno R.S.,Zampieri Dávila,Rodrigues J. Augusto R.,Moran Paulo J.S.

Funder

CNPq

FAPESP

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference35 articles.

1. Stereoselective reduction of (±)-bicyclo[3.3.1]nonane-2,6-dione by microorganisms

2. Enzyme Catalysis in Organic Synthesis;Bougiouku,2012

3. Enantioenriched Compounds via Enzyme-Catalyzed Redox Reactions

4. Asymmetric Reduction of Carbon–Carbon Double Bonds of Conjugated Enones with Fermenting Bakers’ Yeast

5. Stereochemistry of the double bond saturation in the formation in baker's yeast of 4-(4-hydroxyphenyl)-2-butanone (raspberry ketone)

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1. Ene-reductases: Contribution from Brazilian fungi in organic synthesis;Results in Chemistry;2023-01

2. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan;Marine Biotechnology;2020-02-20

3. Regioselectivity Control of Enone Reduction Mediated by Aqueous Baker's Yeast with Addition of Ionic Liquid [bmim(PF 6 )];Biocatalysis and Agricultural Biotechnology;2017-10

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