Asymmetric Bioreduction of β-Activated Vinylphosphonate Derivatives Using Ene-Reductases-Reference-Cited by-同舟云学术

Asymmetric Bioreduction of β-Activated Vinylphosphonate Derivatives Using Ene-Reductases

Published:2017-10-18 Issue:23 Volume:359 Page:4190-4196
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Janicki Ignacy¹,Kiełbasiński Piotr¹,Turrini Nikolaus G.²,Faber Kurt²,Hall Mélanie²

Affiliation:

1. Department of Heteroorganic Chemistry; Centre of Molecular and Macromolecular Studies; Polish Academy of Sciences; Sienkiewicza 112 90-363 Łódź Poland

2. Department of Chemistry; University of Graz; Heinrichstrasse 28 8010 Graz Austria

Funder

National Science Center, Poland

COST Action CM1303 “Systems Biocatalysis”

Innovative Medicines Initiative Joint Undertaking

European Union's Seventh Framework Programme

EFPIA companies

Publisher

Wiley

Subject

General Chemistry

Reference45 articles.

1. SF2312 is a natural phosphonate inhibitor of enolase

2. Radical addition to vinyl phosphonates. A new synthesis of isosteric phosphonates and phosphonate analogues of α-amino acids

3. Phosphonate analogs of chorismic acid: synthesis and evaluation as mechanism-based inactivators of chorismate mutase

4. Biosynthesis of Phosphonic and Phosphinic Acid Natural Products

Cited by 21 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. Ene-Reductase-Catalyzed Enantioselective Desymmetrization of Cyclohexadienones: Straightforward Access to All-Carbon Quaternary Stereocenters;ACS Catalysis;2024-04-08

2. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie International Edition;2023-02-27

3. Catalytic Asymmetric Conjugate Reduction;Angewandte Chemie;2023-02-27

4. Ni-Catalyzed Asymmetric Hydrogenation of α-Substituted α,β-Unsaturated Phosphine Oxides/Phosphonates/Phosphoric Acids;Organic Letters;2023-01-30

5. Introduction of Chiral Centers to α- and/or β-Positions of Carbonyl Groups by Biocatalytic Asymmetric Reduction of α,β-Unsaturated Carbonyl Compounds;Natural Product Communications;2022-05