Uncovering Hydroxynitrile Lyase Variants with Promiscuous Diastereoselective Nitroaldolase Activity toward the Highly Stereocontrolled Synthesis of <i>Anti</i> β-Nitroalcohols-Reference-Cited by-同舟云学术

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Uncovering Hydroxynitrile Lyase Variants with Promiscuous Diastereoselective Nitroaldolase Activity toward the Highly Stereocontrolled Synthesis of Anti β-Nitroalcohols

Published:2024-08-07 Issue:16 Volume:14 Page:12623-12634
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Chatterjee Ayon¹,Priyanka G.²,Prabhu N. Prakash²^ORCID,Padhi Santosh Kumar¹^ORCID

Affiliation:

1. Biocatalysis and Enzyme Engineering Laboratory, Department of Biochemistry, School of Life Sciences, University of Hyderabad, Hyderabad 500 046, India

2. Department of Biotechnology & Bioinformatics, School of Life Sciences, University of Hyderabad, Hyderabad 500 046, India

Funder

Council of Scientific and Industrial Research, India

Science and Engineering Research Board

University of Hyderabad

University Grants Committee

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.4c04000

Reference85 articles.

1. Optical isomers of metaraminol. Synthesis and biological activity

2. l-Erythro-methoxamine is more potent than phenylephrine in effecting contraction of internal anal sphincter in vitro

3. Self-Assembled Asymmetric Catalyst Engaged in a Continuous-Flow Platform: An Anti-Selective Catalytic Asymmetric Nitroaldol Reaction

4. A Modified Preparation Procedure for Carbon Nanotube-Confined Nd/Na Heterobimetallic Catalyst for anti-Selective Catalytic Asymmetric Nitroaldol Reactions

5. Merging Asymmetric Henry Reaction with Organocatalytic Cascade Reaction for the Construction of a Chiral Indolizidine Alkaloid Skeleton

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