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Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases

Over the last decade, the use of biocatalysts has become an attractive alternative to conventional chemical methods, especially for organic synthesis, due to their unusual properties. Among these enzymes, lipases are the most widely used, because they are cheap, easily available, cofactor-free, and...

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Autores principales: Rouillard, Hervé, Deau, Emmanuel, Domon, Lisianne, Chérouvrier, Jean-René, Graber, Marianne, Thiéry, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270989/
https://www.ncbi.nlm.nih.gov/pubmed/24991755
http://dx.doi.org/10.3390/molecules19079215
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author Rouillard, Hervé
Deau, Emmanuel
Domon, Lisianne
Chérouvrier, Jean-René
Graber, Marianne
Thiéry, Valérie
author_facet Rouillard, Hervé
Deau, Emmanuel
Domon, Lisianne
Chérouvrier, Jean-René
Graber, Marianne
Thiéry, Valérie
author_sort Rouillard, Hervé
collection PubMed
description Over the last decade, the use of biocatalysts has become an attractive alternative to conventional chemical methods, especially for organic synthesis, due to their unusual properties. Among these enzymes, lipases are the most widely used, because they are cheap, easily available, cofactor-free, and have broad substrate specificity. Combined to microwave heating in non-aqueous medium, recent results suggest that irradiation may influence the enzyme activity. This Communication reports the benefits of lipases and the microwave irradiation on the kinetic resolution of racemic homochiral (Z)-cyclooct-5-ene-1,2-diol and (Z)-2-acetoxycyclooct-4-enyl acetate. In order to best achieve the kinetic resolution, different parameters were studied including the type of lipase, the temperature, the impact of microwave power compared to conventional heating. Optimization of the reaction parameters lead to the obtainment of highly enriched or enantiopure diols and diesters in a clean, efficient and safe way.
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spelling pubmed-62709892018-12-21 Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases Rouillard, Hervé Deau, Emmanuel Domon, Lisianne Chérouvrier, Jean-René Graber, Marianne Thiéry, Valérie Molecules Article Over the last decade, the use of biocatalysts has become an attractive alternative to conventional chemical methods, especially for organic synthesis, due to their unusual properties. Among these enzymes, lipases are the most widely used, because they are cheap, easily available, cofactor-free, and have broad substrate specificity. Combined to microwave heating in non-aqueous medium, recent results suggest that irradiation may influence the enzyme activity. This Communication reports the benefits of lipases and the microwave irradiation on the kinetic resolution of racemic homochiral (Z)-cyclooct-5-ene-1,2-diol and (Z)-2-acetoxycyclooct-4-enyl acetate. In order to best achieve the kinetic resolution, different parameters were studied including the type of lipase, the temperature, the impact of microwave power compared to conventional heating. Optimization of the reaction parameters lead to the obtainment of highly enriched or enantiopure diols and diesters in a clean, efficient and safe way. MDPI 2014-07-02 /pmc/articles/PMC6270989/ /pubmed/24991755 http://dx.doi.org/10.3390/molecules19079215 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rouillard, Hervé
Deau, Emmanuel
Domon, Lisianne
Chérouvrier, Jean-René
Graber, Marianne
Thiéry, Valérie
Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases
title Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases
title_full Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases
title_fullStr Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases
title_full_unstemmed Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases
title_short Microwave-Assisted Kinetic Resolution of Homochiral (Z)-Cyclooct-5-ene-1,2-diol and (Z)-2-Acetoxycyclooct-4-enyl Acetate Using Lipases
title_sort microwave-assisted kinetic resolution of homochiral (z)-cyclooct-5-ene-1,2-diol and (z)-2-acetoxycyclooct-4-enyl acetate using lipases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270989/
https://www.ncbi.nlm.nih.gov/pubmed/24991755
http://dx.doi.org/10.3390/molecules19079215
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