Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols

Autores
Cuetos, Aníbal; Bisogno, Fabricio Román; Lavandera, Iván; Gotor, Vicente
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A fully convergent one-pot two-step synthesis of different chiral 1,2,3-triazole-derived diols in high yields and excellent enantio- and diastereoselectivities has been achieved under very mild conditions in aqueous medium by combining a single alcohol dehydrogenase (ADH) with a Cu-catalysed ‘click’ reaction.
Fil: Cuetos, Aníbal. Universidad de Oviedo; España
Fil: Bisogno, Fabricio Román. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina. Universidad de Oviedo; España
Fil: Lavandera, Iván. Universidad de Oviedo; España
Fil: Gotor, Vicente. Universidad de Oviedo; España
Materia
Concurrent Catalysis
Click Chemistry
One-Pot Synthesis
Alcohol Dehydrogenases
Convergent Process
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/25005
Acceder
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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diolsCuetos, AníbalBisogno, Fabricio RománLavandera, IvánGotor, VicenteConcurrent CatalysisClick ChemistryOne-Pot SynthesisAlcohol DehydrogenasesConvergent Processhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A fully convergent one-pot two-step synthesis of different chiral 1,2,3-triazole-derived diols in high yields and excellent enantio- and diastereoselectivities has been achieved under very mild conditions in aqueous medium by combining a single alcohol dehydrogenase (ADH) with a Cu-catalysed ‘click’ reaction.Fil: Cuetos, Aníbal. Universidad de Oviedo; EspañaFil: Bisogno, Fabricio Román. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina. Universidad de Oviedo; EspañaFil: Lavandera, Iván. Universidad de Oviedo; EspañaFil: Gotor, Vicente. Universidad de Oviedo; EspañaRoyal Society of Chemistry2013-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/25005Cuetos, Aníbal; Bisogno, Fabricio Román; Lavandera, Iván; Gotor, Vicente; Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols; Royal Society of Chemistry; Chemical Communications; 49; 26; 2-2013; 2625-26271359-7345CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c3cc38674kinfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2013/CC/c3cc38674k#!divAbstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-29T11:47:02Zoai:ri.conicet.gov.ar:11336/25005instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-29 11:47:02.733CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
title Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
spellingShingle Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
Cuetos, Aníbal
Concurrent Catalysis
Click Chemistry
One-Pot Synthesis
Alcohol Dehydrogenases
Convergent Process
title_short Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
title_full Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
title_fullStr Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
title_full_unstemmed Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
title_sort Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
dc.creator.none.fl_str_mv Cuetos, Aníbal
Bisogno, Fabricio Román
Lavandera, Iván
Gotor, Vicente
author Cuetos, Aníbal
author_facet Cuetos, Aníbal
Bisogno, Fabricio Román
Lavandera, Iván
Gotor, Vicente
author_role author
author2 Bisogno, Fabricio Román
Lavandera, Iván
Gotor, Vicente
author2_role author
author
author
dc.subject.none.fl_str_mv Concurrent Catalysis
Click Chemistry
One-Pot Synthesis
Alcohol Dehydrogenases
Convergent Process
topic Concurrent Catalysis
Click Chemistry
One-Pot Synthesis
Alcohol Dehydrogenases
Convergent Process
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv A fully convergent one-pot two-step synthesis of different chiral 1,2,3-triazole-derived diols in high yields and excellent enantio- and diastereoselectivities has been achieved under very mild conditions in aqueous medium by combining a single alcohol dehydrogenase (ADH) with a Cu-catalysed ‘click’ reaction.
Fil: Cuetos, Aníbal. Universidad de Oviedo; España
Fil: Bisogno, Fabricio Román. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina. Universidad de Oviedo; España
Fil: Lavandera, Iván. Universidad de Oviedo; España
Fil: Gotor, Vicente. Universidad de Oviedo; España
description A fully convergent one-pot two-step synthesis of different chiral 1,2,3-triazole-derived diols in high yields and excellent enantio- and diastereoselectivities has been achieved under very mild conditions in aqueous medium by combining a single alcohol dehydrogenase (ADH) with a Cu-catalysed ‘click’ reaction.
publishDate 2013
dc.date.none.fl_str_mv 2013-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/25005
Cuetos, Aníbal; Bisogno, Fabricio Román; Lavandera, Iván; Gotor, Vicente; Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols; Royal Society of Chemistry; Chemical Communications; 49; 26; 2-2013; 2625-2627
1359-7345
CONICET Digital
CONICET
url http://hdl.handle.net/11336/25005
identifier_str_mv Cuetos, Aníbal; Bisogno, Fabricio Román; Lavandera, Iván; Gotor, Vicente; Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols; Royal Society of Chemistry; Chemical Communications; 49; 26; 2-2013; 2625-2627
1359-7345
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1039/c3cc38674k
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2013/CC/c3cc38674k#!divAbstract
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 13.10058

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