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dc.contributor.author
Aguirre Pranzoni, Celeste Beatriz  
dc.contributor.author
Bisogno, Fabricio Román  
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Orden, Alejandro Agustin  
dc.contributor.author
Kurina Sanz, Marcela Beatriz  
dc.date.available
2016-09-14T20:51:12Z  
dc.date.issued
2015-04  
dc.identifier.citation
Aguirre Pranzoni, Celeste Beatriz; Bisogno, Fabricio Román; Orden, Alejandro Agustin; Kurina Sanz, Marcela Beatriz; Lyophilized Rhodotorula yeast as all-in-one redox biocatalyst: Access to enantiopure building blocks by simple chemoenzymatic one-pot procedures; Elsevier Science; Journal Of Molecular Catalysis B-enzymatic; 114; 4-2015; 19-24  
dc.identifier.issn
1381-1177  
dc.identifier.uri
http://hdl.handle.net/11336/7639  
dc.description.abstract
Rhodotorula sp. LSL, isolated from a local landfarming was able to catalyze the reduction of prochiral arylketones into sec-alcohols with excellent Prelog stereoselectivity (ee > 99%). The use of resting and lyophilized cells was optimized accessing to an easy-to-use whole cell biocatalyst that efficiently works even under non-sterile conditions, without the addition of external cofactors and using plain water as solvent. The catalyst resistance in alkaline media enabled (chemo)enzymatic one-pot procedures at high pH values. So a simple and efficient methodology was applied to prepare alternatively enantiopure β-halohydrins, terminal diols and epoxides from aromatic α-haloketones.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
Rhodotorula  
dc.subject
Stereoselective Reduction  
dc.subject
(Chemo)Enzymatic  
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One-Pot Procedures  
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Chiral Alcohols  
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Química Orgánica  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Lyophilized Rhodotorula yeast as all-in-one redox biocatalyst: Access to enantiopure building blocks by simple chemoenzymatic one-pot procedures  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-05-16T20:08:50Z  
dc.journal.volume
114  
dc.journal.pagination
19-24  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Aguirre Pranzoni, Celeste Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Investigaciones En Tecnología Química; Argentina  
dc.description.fil
Fil: Bisogno, Fabricio Román. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto de Investigaciones En Físicoquímica de Córdoba; Argentina  
dc.description.fil
Fil: Orden, Alejandro Agustin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Investigaciones En Tecnología Química; Argentina  
dc.description.fil
Fil: Kurina Sanz, Marcela Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Investigaciones En Tecnología Química; Argentina  
dc.journal.title
Journal Of Molecular Catalysis B-enzymatic  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1381117714002124  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.molcatb.2014.07.011