New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions

Autores
Zanardi, Maria Marta; Botta, María Celeste; Suarez, Alejandra Graciela
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A convenient procedure for the preparation of chiral 1,2-aminoalcohols starting from levoglucosenone, a biomass derivative, is described. The 1,2-aminoalcohols, bearing primary, secondary, and tertiary amino groups, were tested as chiral catalysts in the asymmetric addition of diethyl zinc to benzaldehyde.
Fil: Zanardi, Maria Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Botta, María Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Suarez, Alejandra Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Materia
Levoglucosenone
1,2-Aminoalcohols
Chiral Ligands
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/5998
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/5998
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additionsZanardi, Maria MartaBotta, María CelesteSuarez, Alejandra GracielaLevoglucosenone1,2-AminoalcoholsChiral Ligandshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A convenient procedure for the preparation of chiral 1,2-aminoalcohols starting from levoglucosenone, a biomass derivative, is described. The 1,2-aminoalcohols, bearing primary, secondary, and tertiary amino groups, were tested as chiral catalysts in the asymmetric addition of diethyl zinc to benzaldehyde.Fil: Zanardi, Maria Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaFil: Botta, María Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaFil: Suarez, Alejandra Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaElsevier2014-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/5998Zanardi, Maria Marta; Botta, María Celeste; Suarez, Alejandra Graciela; New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions; Elsevier; Tetrahedron Letters; 55; 42; 9-2014; 5832-58350040-4039enginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403914014774info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.08.124info:eu-repo/semantics/altIdentifier/doi/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:21:32Zoai:ri.conicet.gov.ar:11336/5998instacron: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:34982025-09-10 13:21:32.582CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
title New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
spellingShingle New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
Zanardi, Maria Marta
Levoglucosenone
1,2-Aminoalcohols
Chiral Ligands
title_short New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
title_full New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
title_fullStr New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
title_full_unstemmed New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
title_sort New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions
dc.creator.none.fl_str_mv Zanardi, Maria Marta
Botta, María Celeste
Suarez, Alejandra Graciela
author Zanardi, Maria Marta
author_facet Zanardi, Maria Marta
Botta, María Celeste
Suarez, Alejandra Graciela
author_role author
author2 Botta, María Celeste
Suarez, Alejandra Graciela
author2_role author
author
dc.subject.none.fl_str_mv Levoglucosenone
1,2-Aminoalcohols
Chiral Ligands
topic Levoglucosenone
1,2-Aminoalcohols
Chiral Ligands
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 convenient procedure for the preparation of chiral 1,2-aminoalcohols starting from levoglucosenone, a biomass derivative, is described. The 1,2-aminoalcohols, bearing primary, secondary, and tertiary amino groups, were tested as chiral catalysts in the asymmetric addition of diethyl zinc to benzaldehyde.
Fil: Zanardi, Maria Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Botta, María Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Suarez, Alejandra Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
description A convenient procedure for the preparation of chiral 1,2-aminoalcohols starting from levoglucosenone, a biomass derivative, is described. The 1,2-aminoalcohols, bearing primary, secondary, and tertiary amino groups, were tested as chiral catalysts in the asymmetric addition of diethyl zinc to benzaldehyde.
publishDate 2014
dc.date.none.fl_str_mv 2014-09
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/11336/5998
Zanardi, Maria Marta; Botta, María Celeste; Suarez, Alejandra Graciela; New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions; Elsevier; Tetrahedron Letters; 55; 42; 9-2014; 5832-5835
0040-4039
url http://hdl.handle.net/11336/5998
identifier_str_mv Zanardi, Maria Marta; Botta, María Celeste; Suarez, Alejandra Graciela; New chiral 1,2-aminoalcohols derived from biomass and their application in enantioselective diethyl zinc additions; Elsevier; Tetrahedron Letters; 55; 42; 9-2014; 5832-5835
0040-4039
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403914014774
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.08.124
info:eu-repo/semantics/altIdentifier/doi/
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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
_version_ 1842981182579408896
score 12.48226

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