Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route

Autores
Signorella, Sandra Rosanna; Ledesma, Gabriela Nanci
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Three new unsymmetrical diamino proligands with a central alcohol group and four different pendant arms were obtained, employing a five step synthesis. The synthesis of these compounds involves inexpensive and commercially available reagents. The versatility of the synthetic route allows accessing to compartmental diamines with two chemically different adjacent coordination chambers.
Fil: Signorella, Sandra Rosanna. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
Fil: Ledesma, Gabriela Nanci. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
Materia
BINUCLEATING LIGANDS
CHEMICAL DESIGN
BIOMIMETICS
COMPARTMENTAL DIAMINES
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:11336/104554
Acceder
id CONICETDig_093ac0ca98451492ba4f1434cc4f2748
oai_identifier_str oai:ri.conicet.gov.ar:11336/104554
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible routeSignorella, Sandra RosannaLedesma, Gabriela NanciBINUCLEATING LIGANDSCHEMICAL DESIGNBIOMIMETICSCOMPARTMENTAL DIAMINEShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Three new unsymmetrical diamino proligands with a central alcohol group and four different pendant arms were obtained, employing a five step synthesis. The synthesis of these compounds involves inexpensive and commercially available reagents. The versatility of the synthetic route allows accessing to compartmental diamines with two chemically different adjacent coordination chambers.Fil: Signorella, Sandra Rosanna. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; ArgentinaFil: Ledesma, Gabriela Nanci. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; ArgentinaPergamon-Elsevier Science Ltd2012-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/104554Signorella, Sandra Rosanna; Ledesma, Gabriela Nanci; Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 53; 42; 8-2012; 5699-57020040-4039CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2012.08.057info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0040403912014165info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:35:06Zoai:ri.conicet.gov.ar:11336/104554instacron: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:34982025-09-29 09:35:07.218CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
title Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
spellingShingle Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
Signorella, Sandra Rosanna
BINUCLEATING LIGANDS
CHEMICAL DESIGN
BIOMIMETICS
COMPARTMENTAL DIAMINES
title_short Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
title_full Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
title_fullStr Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
title_full_unstemmed Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
title_sort Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route
dc.creator.none.fl_str_mv Signorella, Sandra Rosanna
Ledesma, Gabriela Nanci
author Signorella, Sandra Rosanna
author_facet Signorella, Sandra Rosanna
Ledesma, Gabriela Nanci
author_role author
author2 Ledesma, Gabriela Nanci
author2_role author
dc.subject.none.fl_str_mv BINUCLEATING LIGANDS
CHEMICAL DESIGN
BIOMIMETICS
COMPARTMENTAL DIAMINES
topic BINUCLEATING LIGANDS
CHEMICAL DESIGN
BIOMIMETICS
COMPARTMENTAL DIAMINES
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Three new unsymmetrical diamino proligands with a central alcohol group and four different pendant arms were obtained, employing a five step synthesis. The synthesis of these compounds involves inexpensive and commercially available reagents. The versatility of the synthetic route allows accessing to compartmental diamines with two chemically different adjacent coordination chambers.
Fil: Signorella, Sandra Rosanna. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
Fil: Ledesma, Gabriela Nanci. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
description Three new unsymmetrical diamino proligands with a central alcohol group and four different pendant arms were obtained, employing a five step synthesis. The synthesis of these compounds involves inexpensive and commercially available reagents. The versatility of the synthetic route allows accessing to compartmental diamines with two chemically different adjacent coordination chambers.
publishDate 2012
dc.date.none.fl_str_mv 2012-08
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/11336/104554
Signorella, Sandra Rosanna; Ledesma, Gabriela Nanci; Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 53; 42; 8-2012; 5699-5702
0040-4039
CONICET Digital
CONICET
url http://hdl.handle.net/11336/104554
identifier_str_mv Signorella, Sandra Rosanna; Ledesma, Gabriela Nanci; Chemical design and synthesis of unsymmetrical diamino proligands employing a flexible route; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 53; 42; 8-2012; 5699-5702
0040-4039
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2012.08.057
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0040403912014165
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
dc.publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
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_ 1844613090930327552
score 13.070432

Publicaciones similares