Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/127808
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DC Field | Value | Language |
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dc.contributor.author | Solé Arjó, Daniel | - |
dc.contributor.author | Pérez Janer, Ferran | - |
dc.contributor.author | Zulaica Gallego, Ester | - |
dc.contributor.author | Guastavino, Javier F. | - |
dc.contributor.author | Fernández Cadenas, Israel | - |
dc.date.accessioned | 2019-02-01T12:19:54Z | - |
dc.date.available | 2019-02-01T12:19:54Z | - |
dc.date.issued | 2016-01-28 | - |
dc.identifier.issn | 2155-5435 | - |
dc.identifier.uri | https://hdl.handle.net/2445/127808 | - |
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. Keywords: arylation; density functional calculations; domino reactions; indoles; palladium-catalyzed | - |
dc.format.extent | 10 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | American Chemical Society | - |
dc.relation.isformatof | Versió postprint del document publicat a: https://doi.org/10.1021/acscatal.6b00027 | - |
dc.relation.ispartof | ACS Catalysis, 2016, vol. 6, num. 3, p. 1691-1700 | - |
dc.relation.uri | https://doi.org/10.1021/acscatal.6b00027 | - |
dc.rights | (c) American Chemical Society , 2016 | - |
dc.source | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) | - |
dc.subject.classification | Pal·ladi (Element químic) | - |
dc.subject.classification | Catàlisi | - |
dc.subject.classification | Teoria del funcional de densitat | - |
dc.subject.classification | Compostos heterocíclics | - |
dc.subject.classification | Síntesi orgànica | - |
dc.subject.other | Palladium | - |
dc.subject.other | Catalysis | - |
dc.subject.other | Density functionals | - |
dc.subject.other | Heterocyclic compounds | - |
dc.subject.other | Organic synthesis | - |
dc.title | Pd-Catalyzed α-Arylation of Sulfones in a Three-Component Synthesis of 3-[2-(Phenyl/methylsulfonyl)ethyl]indoles | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/acceptedVersion | - |
dc.identifier.idgrec | 661320 | - |
dc.date.updated | 2019-02-01T12:19:54Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
Appears in Collections: | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) |
Files in This Item:
File | Description | Size | Format | |
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661320.pdf | 1.69 MB | Adobe PDF | View/Open |
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