Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts
- Autores
- Traficante, Carla Inés; Mata, Ernesto Gabino; Delpiccolo, Carina Maria Lujan
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A very high-yielding Pd-catalyzed cross-coupling between aryl halides and aryl(trialkoxy)silanes is achieved in the presence of Cu(i) and a measured amount of water. This novel methodology is useful for the generation of a wide range of biaryls, particularly non-para substituted derivatives, which are usually less reported.
Fil: Traficante, Carla Inés. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Mata, Ernesto Gabino. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Delpiccolo, Carina Maria Lujan. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina - Materia
-
Cross-coupling reactions
Biaryl derivatives
Hiyama coupling - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/127128
Ver los metadatos del registro completo
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Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) saltsTraficante, Carla InésMata, Ernesto GabinoDelpiccolo, Carina Maria LujanCross-coupling reactionsBiaryl derivativesHiyama couplinghttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A very high-yielding Pd-catalyzed cross-coupling between aryl halides and aryl(trialkoxy)silanes is achieved in the presence of Cu(i) and a measured amount of water. This novel methodology is useful for the generation of a wide range of biaryls, particularly non-para substituted derivatives, which are usually less reported.Fil: Traficante, Carla Inés. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaFil: Mata, Ernesto Gabino. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaFil: Delpiccolo, Carina Maria Lujan. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaRoyal Society of Chemistry2015-03info: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/11336/127128Traficante, Carla Inés; Mata, Ernesto Gabino; Delpiccolo, Carina Maria Lujan; Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts; Royal Society of Chemistry; RSC Advances; 5; 34; 3-2015; 26796-268002046-2069CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c5ra03732hinfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2015/RA/C5RA03732H#!divAbstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-12T09:33:57Zoai:ri.conicet.gov.ar:11336/127128instacron: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:34982025-11-12 09:33:58.058CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| title |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| spellingShingle |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts Traficante, Carla Inés Cross-coupling reactions Biaryl derivatives Hiyama coupling |
| title_short |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| title_full |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| title_fullStr |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| title_full_unstemmed |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| title_sort |
Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts |
| dc.creator.none.fl_str_mv |
Traficante, Carla Inés Mata, Ernesto Gabino Delpiccolo, Carina Maria Lujan |
| author |
Traficante, Carla Inés |
| author_facet |
Traficante, Carla Inés Mata, Ernesto Gabino Delpiccolo, Carina Maria Lujan |
| author_role |
author |
| author2 |
Mata, Ernesto Gabino Delpiccolo, Carina Maria Lujan |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Cross-coupling reactions Biaryl derivatives Hiyama coupling |
| topic |
Cross-coupling reactions Biaryl derivatives Hiyama coupling |
| 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 very high-yielding Pd-catalyzed cross-coupling between aryl halides and aryl(trialkoxy)silanes is achieved in the presence of Cu(i) and a measured amount of water. This novel methodology is useful for the generation of a wide range of biaryls, particularly non-para substituted derivatives, which are usually less reported. Fil: Traficante, Carla Inés. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina Fil: Mata, Ernesto Gabino. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina Fil: Delpiccolo, Carina Maria Lujan. 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. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina |
| description |
A very high-yielding Pd-catalyzed cross-coupling between aryl halides and aryl(trialkoxy)silanes is achieved in the presence of Cu(i) and a measured amount of water. This novel methodology is useful for the generation of a wide range of biaryls, particularly non-para substituted derivatives, which are usually less reported. |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015-03 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/127128 Traficante, Carla Inés; Mata, Ernesto Gabino; Delpiccolo, Carina Maria Lujan; Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts; Royal Society of Chemistry; RSC Advances; 5; 34; 3-2015; 26796-26800 2046-2069 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/127128 |
| identifier_str_mv |
Traficante, Carla Inés; Mata, Ernesto Gabino; Delpiccolo, Carina Maria Lujan; Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling: The role of water and copper(I) salts; Royal Society of Chemistry; RSC Advances; 5; 34; 3-2015; 26796-26800 2046-2069 CONICET Digital CONICET |
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eng |
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eng |
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Royal Society of Chemistry |
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Royal Society of Chemistry |
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