Mostrar el registro sencillo del ítem
dc.contributor.author
Solé, Daniel
dc.contributor.author
Pérez Janer, Ferran
dc.contributor.author
Zulaica, Ester
dc.contributor.author
Guastavino, Javier Fernando
dc.contributor.author
Fernádez, Israel
dc.date.available
2017-07-04T18:54:10Z
dc.date.issued
2016-02
dc.identifier.citation
Solé, Daniel; Pérez Janer, Ferran; Zulaica, Ester; Guastavino, Javier Fernando; Fernádez, Israel; Pd-Catalyzed alfa-Arylation of Sulfones in a Three-Component Synthesis 3-[2-(phenyl/methylsulfonyl)ethyl]indoles; American Chemical Society; ACS Catalysis; 6; 3; 2-2016; 1691-1700
dc.identifier.issn
2155-5435
dc.identifier.uri
http://hdl.handle.net/11336/19491
dc.description.abstract
A novel four-step domino process for the synthesis of 3-[2-(aryl/alkylsulfonyl)ethyl]indoles starting from readily available 2-iodoanilines is reported. The domino reaction is based on the intramolecular palladium-catalyzed α-arylation of sulfones, which was combined with both intermolecular aza-Michael and Michael addition reactions using vinyl sulfones as the electrophile. The domino process produced good yields and tolerated the presence of substituents with different electronic properties on the aniline ring. In addition, density functional theory (DFT) calculations were carried out to gain more insight into the formation of the observed indole derivatives
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Palladium-Catalyzed
dc.subject
Arylation
dc.subject
Domino Reactions
dc.subject
Indoles
dc.subject
Density Functional Calculations
dc.subject.classification
Química Orgánica
dc.subject.classification
Ciencias Químicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
Pd-Catalyzed alfa-Arylation of Sulfones in a Three-Component Synthesis 3-[2-(phenyl/methylsulfonyl)ethyl]indoles
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2017-06-08T19:27:52Z
dc.journal.volume
6
dc.journal.number
3
dc.journal.pagination
1691-1700
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Washington
dc.description.fil
Fil: Solé, Daniel. Universidad de Barcelona; España
dc.description.fil
Fil: Pérez Janer, Ferran. Universidad de Barcelona; España
dc.description.fil
Fil: Zulaica, Ester. Universidad de Barcelona; España
dc.description.fil
Fil: Guastavino, Javier Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina
dc.description.fil
Fil: Fernádez, Israel. Universidad de Barcelona; España. Universidad Complutense de Madrid; España
dc.journal.title
ACS Catalysis
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acscatal.6b00027
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/acscatal.6b00027
Archivos asociados