Enantiocomplementary Asymmetric Reduction of 2–Haloacetophenones Using <i>Te</i>SADH: Synthesis of Enantiopure 2-Halo-1-arylethanols-Reference-Cited by-同舟云学术

Enantiocomplementary Asymmetric Reduction of 2–Haloacetophenones Using TeSADH: Synthesis of Enantiopure 2-Halo-1-arylethanols

Published:2024-07-29 Issue:32 Volume:9 Page:35046-35051
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Abdulrasheed Muhammad¹,Sardauna Auwal Eshi¹,Alhaffar Mouheddin T.¹²,Takahashi Masateru³,Takahashi Etsuko³,Hamdan Samir M.³^ORCID,Musa Musa M.¹⁴^ORCID

Affiliation:

1. Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran 31261, Saudi Arabia

2. Interdisciplinary Research Center for Advanced Materials, King Fahd University of Petroleum and Minerals, Dhahran 31261, Saudi Arabia

3. Bioscience Program, Division of Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia

4. Interdisciplinary Research Center for Refining and Advanced Chemicals, King Fahd University of Petroleum and Minerals, Dhahran 31261, Saudi Arabia

Funder

King Fahd University of Petroleum and Minerals

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.4c05151

Reference40 articles.

1. Engineering of Candida glabrata Ketoreductase 1 for Asymmetric Reduction of α-Halo Ketones

2. Structure-guided stereoselectivity inversion of a short-chain dehydrogenase/reductase towards halogenated acetophenones

3. Efficient Biocatalytic Synthesis of (R)-2-Chloro-1-(3,4-difluorophenyl)ethanol by the Short-Chain Dehydrogenase PpKR8 from Paraburkholderia phymatum STM815

4. Synthesis of Enantiopure Fluorohydrins Using Alcohol Dehydrogenases at High Substrate Concentrations

5. Discovery of a Switch Between Prelog and Anti-Prelog Reduction toward Halogen-Substituted Acetophenones in Short-Chain Dehydrogenase/Reductases