Glyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids-Reference-Cited by-同舟云学术

Glyoxalase-based toolbox for the enantioselective synthesis of α-hydroxy carboxylic acids

Published:2024 Issue:13 Volume:22 Page:2539-2543
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yedigenov Mussa¹^ORCID,Amire Niyaz¹,Abdirassil Aizat¹^ORCID,Mulikova Tomiris¹,Begenov Azamat¹,Kiesilä Anniina²,Peshkov Anatoly A.¹,Peshkov Vsevolod A.¹²,Utepbergenov Darkhan¹^ORCID

Affiliation:

1. Department of Chemistry, School of Sciences and Humanities, Nazarbayev University, 53 Kabanbay Batyr Ave, Astana, 010000, Kazakhstan

2. Department of Chemistry, University of Jyväskylä, Survontie 9 B, FI-40014, Finland

Abstract

Glyoxalases DJ-1 and GlxI/II were used for the enantioselective conversion of 13 (hetero)aryl glyoxals to l- and d-α-hydroxy carboxylic acids, respectively.

Funder

Nazarbayev University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB02098C

Reference45 articles.

1. G. M.Coppola and H. F.Schuster , alpha-Hydroxy Acids in Enantioselective Syntheses , Wiley , 2003

2. The Synthesis of Chiral α-Aryl α-Hydroxy Carboxylic Acids via RuPHOX-Ru Catalyzed Asymmetric Hydrogenation

3. Direct asymmetric hydrogenation of α-keto acids by using the highly efficient chiral spiro iridium catalysts

4. Dynamic Kinetic Resolution via Dual-Function Catalysis of Modified Cinchona Alkaloids: Asymmetric Synthesis of α-Hydroxy Carboxylic Acids

5. Efficient Intramolecular Asymmetric Reductions of α-, β-, and γ-Keto Acids with Diisopinocampheylborane1

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