Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction

Autores
Mangione, Maria Ines; Spanevello, Rolando Angel
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers.
Fil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Spanevello, Rolando Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Materia
Fluorenone
Carbazole
Ullmann Coupling
Dendrimers
Oled
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:11336/6009

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network_name_str CONICET Digital (CONICET)
spelling Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reactionMangione, Maria InesSpanevello, Rolando AngelFluorenoneCarbazoleUllmann CouplingDendrimersOledhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers.Fil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaFil: Spanevello, Rolando Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; ArgentinaElsevier2014-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/6009Mangione, Maria Ines; Spanevello, Rolando Angel; Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction; Elsevier; Tetrahedron Letters; 56; 2; 12-2014; 465-4670040-4039enginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403914020474info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.11.133info: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 Técnicas2025-09-29T09:34:31Zoai:ri.conicet.gov.ar:11336/6009instacron: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 09:34:31.953CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
title Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
spellingShingle Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
Mangione, Maria Ines
Fluorenone
Carbazole
Ullmann Coupling
Dendrimers
Oled
title_short Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
title_full Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
title_fullStr Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
title_full_unstemmed Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
title_sort Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction
dc.creator.none.fl_str_mv Mangione, Maria Ines
Spanevello, Rolando Angel
author Mangione, Maria Ines
author_facet Mangione, Maria Ines
Spanevello, Rolando Angel
author_role author
author2 Spanevello, Rolando Angel
author2_role author
dc.subject.none.fl_str_mv Fluorenone
Carbazole
Ullmann Coupling
Dendrimers
Oled
topic Fluorenone
Carbazole
Ullmann Coupling
Dendrimers
Oled
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers.
Fil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
Fil: Spanevello, Rolando Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina
description Two novel aromatic molecules were synthesized via a modified Ullmann coupling starting from a known compound 2,7-diiodofluorenone with carbazole derivatives. These compounds were obtained in very good yields. Due to their fluorophore components, like fluorenone and carbazole, they could be applied as scaffolds for the development of organic materials like dendrimers and polymers.
publishDate 2014
dc.date.none.fl_str_mv 2014-12
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/11336/6009
Mangione, Maria Ines; Spanevello, Rolando Angel; Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction; Elsevier; Tetrahedron Letters; 56; 2; 12-2014; 465-467
0040-4039
url http://hdl.handle.net/11336/6009
identifier_str_mv Mangione, Maria Ines; Spanevello, Rolando Angel; Synthesis of nitrogenated scaffolds derived from fluorene by a modified Ullmann type reaction; Elsevier; Tetrahedron Letters; 56; 2; 12-2014; 465-467
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/S0040403914020474
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.11.133
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
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
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score 13.070432