An efficient and new protocol for phosphine-free Suzuki coupling reaction using palladium-encapsulated and air-stable MIDA boronates in an aqueous medium

dc.creatorMendes da Silva, Joaquim Fernando
dc.creatorYepes Pérez, Andres Felipe
dc.creatorPinto de Almeida, Natália
dc.date2019-08-08T22:14:43Z
dc.date2019-08-08T22:14:43Z
dc.date2014
dc.date.accessioned2020-09-21T21:49:28Z
dc.date.available2020-09-21T21:49:28Z
dc.identifier2046-2069
dc.identifierhttp://repositorio.udes.edu.co/handle/001/3553
dc.identifier10.1039/c4ra03586k
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3177572
dc.descriptionA simple methodology that uses a system based on polyurea microencapsulated palladium (PdEnCat 30™) and aryl or (2-pyridyl) MIDA boronates for Suzuki–Miyaura cross-coupling reactions of (hetero)aryl halides in water–alcohol under phosphine-free conditions was developed.
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dc.languageeng
dc.relationRSC Advances
dc.rightsDerechos Reservados - The Authors, 2014
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAtribución-NoComercial
dc.sourcehttps://pubs.rsc.org/en/content/articlelanding/2014/ra/c4ra03586k#!divAbstract
dc.subjectpalladium-encapsulated
dc.subjectMIDA
dc.titleAn efficient and new protocol for phosphine-free Suzuki coupling reaction using palladium-encapsulated and air-stable MIDA boronates in an aqueous medium
dc.typeArtículo de revista
dc.typeImage
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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