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DUGi: Ítem | DUGiDocs - Dehydrogenative [2 + 2 + 2] Cycloaddition of Cyano-yne-allene Substrates: Convenient Access to 2,6-Naphthyridine Scaffolds

Ítem


Dehydrogenative [2 + 2 + 2] Cycloaddition of Cyano-yne-allene Substrates: Convenient Access to 2,6-Naphthyridine Scaffolds

A rhodium-catalyzed [2 + 2 + 2] cycloaddition of cyano-yne-allene scaffolds followed by a dehydrogenative process enabling the direct synthesis of unsaturated pyridine-containing compounds that can be conveniently converted to 2,6-naphthyridine derivatives is reported

Financial support from the Spanish Ministry of Education and Science (MINECO) (Project No. CTQ2011-23121, CTQ2014-54306-P, and a RyC contract to A.L.) and the DIUE of the Generalitat de Catalunya (Project No. 2014SGR931) are acknowledged

info:eu-repo/grantAgreement/MINECO//CTQ2014-54306-P/ES/ESTUDIOS TEORICO-EXPERIMENTALES DE CICLACIONES CATALIZADAS POR METALES DE TRANSICION. NUEVOS DESARROLLOS EN AROMATICIDAD, FUNCIONALES DE LA DENSIDAD Y QUIMICA SUPRAMOLECULAR/

info:eu-repo/grantAgreement/MICINN//CTQ2011-23121/ES/APLICACIONES CATALITICAS DE COMPUESTOS DE RODIO, PALADIO Y NIQUEL EN SINTESIS ORGANICA. METODOLOGIA Y ESTUDIOS MECANISTICOS./

American Chemical Society (ACS)

Director: Ministerio de Economía y Competitividad (Espanya)
Ministerio de Ciencia e Innovación (Espanya)
Generalitat de Catalunya. Agència de Gestió d’Ajuts Universitaris i de Recerca
Autor: Haraburda, Ewelina
Lledó Ponsati, Agustí
Roglans i Ribas, Anna
Pla i Quintana, Anna
Resum: A rhodium-catalyzed [2 + 2 + 2] cycloaddition of cyano-yne-allene scaffolds followed by a dehydrogenative process enabling the direct synthesis of unsaturated pyridine-containing compounds that can be conveniently converted to 2,6-naphthyridine derivatives is reported
Financial support from the Spanish Ministry of Education and Science (MINECO) (Project No. CTQ2011-23121, CTQ2014-54306-P, and a RyC contract to A.L.) and the DIUE of the Generalitat de Catalunya (Project No. 2014SGR931) are acknowledged
Format: application/pdf
Accés al document: http://hdl.handle.net/10256/10958
Llenguatge: eng
Editor: American Chemical Society (ACS)
Col·lecció: info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.orglett.5b01554
info:eu-repo/semantics/altIdentifier/issn/1523-7060
info:eu-repo/semantics/altIdentifier/eissn/1523-7052
AGAUR/2014-2016/2014 SGR-931
És part de: info:eu-repo/grantAgreement/MINECO//CTQ2014-54306-P/ES/ESTUDIOS TEORICO-EXPERIMENTALES DE CICLACIONES CATALIZADAS POR METALES DE TRANSICION. NUEVOS DESARROLLOS EN AROMATICIDAD, FUNCIONALES DE LA DENSIDAD Y QUIMICA SUPRAMOLECULAR/
info:eu-repo/grantAgreement/MICINN//CTQ2011-23121/ES/APLICACIONES CATALITICAS DE COMPUESTOS DE RODIO, PALADIO Y NIQUEL EN SINTESIS ORGANICA. METODOLOGIA Y ESTUDIOS MECANISTICOS./
Drets: Tots els drets reservats
Matèria: Reaccions d’addició
Addition reactions
Catàlisi
Catalysis
Catalitzadors de rodi
Rhodium catalyst
Rodi
Rhodium
Ciclització (Química)
Ring formation (Chemistry)
Títol: Dehydrogenative [2 + 2 + 2] Cycloaddition of Cyano-yne-allene Substrates: Convenient Access to 2,6-Naphthyridine Scaffolds
Tipus: info:eu-repo/semantics/article
Repositori: DUGiDocs

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