dc.creatorTraficante, Carla Inés
dc.creatorFagundez, Catherine
dc.creatorSerra, Gloria L.
dc.creatorMata, Ernesto Gabino
dc.creatorDelpiccolo, Carina Maria Lujan
dc.date.accessioned2018-09-27T14:37:47Z
dc.date.accessioned2018-11-06T14:43:03Z
dc.date.available2018-09-27T14:37:47Z
dc.date.available2018-11-06T14:43:03Z
dc.date.created2018-09-27T14:37:47Z
dc.date.issued2016-05
dc.identifierTraficante, Carla Inés; Fagundez, Catherine; Serra, Gloria L.; Mata, Ernesto Gabino; Delpiccolo, Carina Maria Lujan; Chemoselective and Sequential Palladium-Catalyzed Couplings for the Generation of Stilbene Libraries via Immobilized Substrates; American Chemical Society; ACS Combinatorial Science; 18; 5; 5-2016; 225-229
dc.identifier2156-8952
dc.identifierhttp://hdl.handle.net/11336/61031
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1889394
dc.description.abstractA versatile palladium-catalyzed tandem synthetic sequence to afford E-stilbenes libraries has been developed. Excellent regio- and stereocontrol have been achieved by means of the sequence of Hiyama and Heck cross-couplings. Undesirable homocoupling byproducts were avoided employing immobilized substrates.
dc.languageeng
dc.publisherAmerican Chemical Society
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acscombsci.6b00023
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acscombsci.6b00023
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectHECK COUPLING
dc.subjectHIYAMA COUPLING
dc.subjectPALLADIUM CROSS-COUPLING REACTIONS
dc.subjectSOLID-PHASE ORGANIC SYNTHESIS
dc.titleChemoselective and Sequential Palladium-Catalyzed Couplings for the Generation of Stilbene Libraries via Immobilized Substrates
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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