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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  
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Arylation  
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Domino Reactions  
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Indoles  
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Density Functional Calculations  
dc.subject.classification
Química Orgánica  
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Ciencias Químicas  
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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