Diastereoselective and enantioselective alkaline-hydrolysis of 2-aryl-1-cyclohexyl acetate: a CAL-B catalyzed deacylation/acylation tandem process-Reference-Cited by-同舟云学术

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Diastereoselective and enantioselective alkaline-hydrolysis of 2-aryl-1-cyclohexyl acetate: a CAL-B catalyzed deacylation/acylation tandem process

Published:2017-11 Issue:11 Volume:28 Page:1644-1650
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Belkacemi Fatma Zahra,Merabet-Khelassi Mounia,Aribi-Zouioueche Louisa,Riant Olivier

Funder

Algerian Ministry of Higher Education and Scientific Research

Catholic University of Louvain

FNRS

Wallonie-Bruxelles International

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference37 articles.

1. Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions,2011

2. Lipases: Useful biocatalysts for the preparation of pharmaceuticals

3. Lipase-mediated chiral resolution of racemates in organic solvents

4. trans-2-Phenylcyclohexanol. A powerful and readily available chiral auxiliary

5. Trans-2-Arylcyclohexanols: Use as auxiliaries in the mukaiyama aldol-type condensation between silyl enol esters and aldehydes

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3. Enantioselective bio-deacylation of arylalkyl acetates using tertiary amines as additive under promiscuous conditions;Enzyme and Microbial Technology;2023-01

4. Practical access to (S)-heterocyclic aromatic acetates via CAL-B/Na₂CO₃-deacylation and Mitsunobu reaction protocol;Biocatalysis and Biotransformation;2022-01-31

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