Biocatalytic asymmetric ring-opening of <i>meso</i>-epoxides to enantiopure cyclic <i>trans</i>-β-amino alcohols involving a key amine transaminase-Reference-Cited by-同舟云学术

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Biocatalytic asymmetric ring-opening of meso-epoxides to enantiopure cyclic trans-β-amino alcohols involving a key amine transaminase

Published:2024 Issue:10 Volume:26 Page:6160-6171
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhang Jingqi¹²,Gao Hang¹^ORCID,Gao Lili²,Chen Mengyi¹,Huang Shuangping¹,Zhang Jiandong¹^ORCID

Affiliation:

1. Department of Biological and Pharmaceutical Engineering, College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan, Shanxi 030024, China

2. College of Environmental Science and Engineering, Taiyuan University of Technology, Taiyuan, Shanxi 030024, China

Abstract

Biocatalytic asymmetric ring-opening of meso-epoxides to chiral cyclic β-amino alcohols with good conversions and excellent enantioselectivity.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/GC/D4GC00827H

Reference58 articles.

1. Folding Propensity of Cyclohexylether-δ-peptides

2. (1S,2R/1R,2S)-Aminocyclohexyl Glycyl Thymine PNA: Synthesis, Monomer Crystal Structures, and DNA/RNA Hybridization Studies

3. Cycloalkanediamine derivatives as novel blood coagulation factor Xa inhibitors

4. Cyclic trans-β-amino alcohols: preparation and enzymatic kinetic resolution

5. Resolution of racemic cis-1-amino-2-indanol by diastereomeric salt formation with (S)-2-phenylpropionic acid

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