A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes

Coupling of alkynyl moieties to heterocyclic rings, without using ransition metals, can be easily performed by the reaction of aryl or heteroaryl sulfonylacetylenes with heteroaryl-Li compounds or their corresponding less reactive magnesium derivatives

Detalles Bibliográficos
Autores: Marzo, Leyre, Pérez, Ignacio, Yuste, Francisco, Alemán Lara, José Julián, García Ruano, José Luis
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/670582
Acceso en línea:http://hdl.handle.net/10486/670582
https://dx.doi.org/10.1039/C4CC07574A
Access Level:acceso abierto
Palabra clave:Acetylene derivative
Lithium
Magnesium
Sulfone derivative
Alkyne
Heterocyclic compound
Química
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spelling A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenesMarzo, LeyrePérez, IgnacioYuste, FranciscoAlemán Lara, José JuliánGarcía Ruano, José LuisAcetylene derivativeLithiumMagnesiumSulfone derivativeAlkyneHeterocyclic compoundQuímicaCoupling of alkynyl moieties to heterocyclic rings, without using ransition metals, can be easily performed by the reaction of aryl or heteroaryl sulfonylacetylenes with heteroaryl-Li compounds or their corresponding less reactive magnesium derivativesFinancial support from the Spanish Government (CTQ2012-35957)The Royal Society of ChemistryDepartamento de Química OrgánicaFacultad de Ciencias20152015-11-05research articlehttp://purl.org/coar/resource_type/c_2df8fbb1VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10486/670582https://dx.doi.org/10.1039/C4CC07574Areponame:Biblos-e Archivo. Repositorio Institucional de la UAMinstname:Universidad Autónoma de MadridInglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:repositorio.uam.es:10486/6705822026-06-23T12:46:27Z
dc.title.none.fl_str_mv A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
title A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
spellingShingle A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
Marzo, Leyre
Acetylene derivative
Lithium
Magnesium
Sulfone derivative
Alkyne
Heterocyclic compound
Química
title_short A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
title_full A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
title_fullStr A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
title_full_unstemmed A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
title_sort A straightforward alkynylation of Li and Mg metalated heterocycles with sulfonylacetylenes
dc.creator.none.fl_str_mv Marzo, Leyre
Pérez, Ignacio
Yuste, Francisco
Alemán Lara, José Julián
García Ruano, José Luis
author Marzo, Leyre
author_facet Marzo, Leyre
Pérez, Ignacio
Yuste, Francisco
Alemán Lara, José Julián
García Ruano, José Luis
author_role author
author2 Pérez, Ignacio
Yuste, Francisco
Alemán Lara, José Julián
García Ruano, José Luis
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Departamento de Química Orgánica
Facultad de Ciencias
dc.subject.none.fl_str_mv Acetylene derivative
Lithium
Magnesium
Sulfone derivative
Alkyne
Heterocyclic compound
Química
topic Acetylene derivative
Lithium
Magnesium
Sulfone derivative
Alkyne
Heterocyclic compound
Química
description Coupling of alkynyl moieties to heterocyclic rings, without using ransition metals, can be easily performed by the reaction of aryl or heteroaryl sulfonylacetylenes with heteroaryl-Li compounds or their corresponding less reactive magnesium derivatives
publishDate 2015
dc.date.none.fl_str_mv 2015
2015-11-05
dc.type.none.fl_str_mv research article
http://purl.org/coar/resource_type/c_2df8fbb1
VoR
http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv http://hdl.handle.net/10486/670582
https://dx.doi.org/10.1039/C4CC07574A
url http://hdl.handle.net/10486/670582
https://dx.doi.org/10.1039/C4CC07574A
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv The Royal Society of Chemistry
publisher.none.fl_str_mv The Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:Biblos-e Archivo. Repositorio Institucional de la UAM
instname:Universidad Autónoma de Madrid
instname_str Universidad Autónoma de Madrid
reponame_str Biblos-e Archivo. Repositorio Institucional de la UAM
collection Biblos-e Archivo. Repositorio Institucional de la UAM
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15,301603

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