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Biocatalysis at Extreme Temperatures: Enantioselective Synthesis of both Enantiomers of Mandelic Acid by Transesterification Catalyzed by a Thermophilic Lipase in Ionic Liquids at 120 °C

dc.contributor.authorRamos-Martín, Jesús
dc.contributor.authorKhiari, Oussama
dc.contributor.authorAlcántara León, Andrés Rafael
dc.contributor.authorSánchez Montero, José
dc.date.accessioned2024-01-11T13:48:33Z
dc.date.available2024-01-11T13:48:33Z
dc.date.issued2020-09-14
dc.descriptionThis article belongs to the Special Issue Applied Biocatalysis in Europe: A Sustainable Tool for Improving Life Quality
dc.description.abstractThe use of biocatalysts in organic chemistry for catalyzing chemo-, regio- and stereoselective transformations has become an usual tool in the last years, both at lab and industrial scale. This is not only because of their exquisite precision, but also due to the inherent increase in the process sustainability. Nevertheless, most of the interesting industrial reactions involve water-insoluble substrates, so the use of (generally not green) organic solvents is generally required. Although lipases are capable of maintaining their catalytic precision working in those solvents, reactions are usually very slow and consequently not very appropriate for industrial purposes. Increasing reaction temperature would accelerate the reaction rate, but this should require the use of lipases from thermophiles, which tend to be more enantioselective at lower temperatures, as they are more rigid than those from mesophiles. Therefore, the ideal scenario would require a thermophilic lipase capable of retaining high enantioselectivity at high temperatures. In this paper, we describe the use of lipase from Geobacillus thermocatenolatus as catalyst in the ethanolysis of racemic 2-(butyryloxy)-2-phenylacetic to furnish both enantiomers of mandelic acid, an useful intermediate in the synthesis of many drugs and active products. The catalytic performance at high temperature in a conventional organic solvent (isooctane) and four imidazolium-based ionic liquids was assessed. The best results were obtained using 1-ethyl-3-methyl imidazolium tetrafluoroborate (EMIMBF4) and 1-ethyl-3-methyl imidazolium hexafluorophosphate (EMIMPF6) at temperatures as high as 120 °C, observing in both cases very fast and enantioselective kinetic resolutions, respectively leading exclusively to the (S) or to the (R)-enantiomer of mandelic acid, depending on the anion component of the ionic liquid.
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipBanco Santander
dc.description.sponsorshipUniversidad Complutense de Madrid
dc.description.sponsorshipMinisterio de Economía, Comercio y Empresa
dc.description.statuspub
dc.identifier.citationRamos-Martín, J.; Khiari, O.; Alcántara, A.R.; Sánchez-Montero, J.M. Biocatalysis at Extreme Temperatures: Enantioselective Synthesis of both Enantiomers of Mandelic Acid by Transesterification Catalyzed by a Thermophilic Lipase in Ionic Liquids at 120 °C. Catalysts 2020, 10, 1055. https://doi.org/10.3390/catal10091055
dc.identifier.doi10.3390/catal10091055
dc.identifier.issn2073-4344
dc.identifier.officialurlhttps://doi.org/10.3390/catal10091055
dc.identifier.urihttps://hdl.handle.net/20.500.14352/92557
dc.issue.number9
dc.journal.titleCatalysts
dc.language.isoeng
dc.page.initial1055
dc.page.total19
dc.publisherMDPI
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/CTQ2017-86170-R
dc.relation.projectIDinfo:eu-repo/grantAgreement/PR87/19-22676
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu6
dc.subject.cdu001.891.5
dc.subject.keywordGeobacillus thermocatenolatus
dc.subject.keywordlipases
dc.subject.keywordethanolysis
dc.subject.keywordionic liquids
dc.subject.keywordkinetic resolution
dc.subject.keywordmandelic acid
dc.subject.ucmCiencias
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco23 Química
dc.subject.unesco24 Ciencias de la Vida
dc.titleBiocatalysis at Extreme Temperatures: Enantioselective Synthesis of both Enantiomers of Mandelic Acid by Transesterification Catalyzed by a Thermophilic Lipase in Ionic Liquids at 120 °C
dc.typejournal article
dc.type.hasVersionAM
dc.volume.number10
dspace.entity.typePublication
relation.isAuthorOfPublicationc0d1193e-3161-4c69-af69-830b32f61932
relation.isAuthorOfPublicationace9b864-c472-4f38-86ba-9a09f24dadb9
relation.isAuthorOfPublication.latestForDiscoveryace9b864-c472-4f38-86ba-9a09f24dadb9

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