Transmetallations between aryltrialkyltins and borane: Synthesis of arylboronic acids and organotin hydrides

dc.creatorFaraoni, María Belén
dc.creatorKoll, Liliana Cristina
dc.creatorMandolesi, Sandra Delia
dc.creatorZuñiga, Adriana Elena
dc.creatorPodestá, Julio Cesar
dc.date.accessioned2021-04-13T18:17:47Z
dc.date.accessioned2022-10-15T07:08:46Z
dc.date.available2021-04-13T18:17:47Z
dc.date.available2022-10-15T07:08:46Z
dc.date.created2021-04-13T18:17:47Z
dc.date.issued2000-11-03
dc.identifierFaraoni, María Belén; Koll, Liliana Cristina; Mandolesi, Sandra Delia; Zuñiga, Adriana Elena; Podestá, Julio Cesar; Transmetallations between aryltrialkyltins and borane: Synthesis of arylboronic acids and organotin hydrides; Elsevier Science SA; Journal of Organometallic Chemistry; 613; 2; 3-11-2000; 236-238
dc.identifier0022-328X
dc.identifierhttp://hdl.handle.net/11336/129952
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4358792
dc.description.abstractAryltrialkyltin compounds react with borane in THF to give mixtures of trialkyltin hydrides and arylboranes, which on hydrolysis give arylboronic acid in high yields. The arylboronic acids are easily separated and obtained free of organotins.
dc.languageeng
dc.publisherElsevier Science SA
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0022328X00005362
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/S0022-328X(00)00536-2
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectARYLBORONIC ACIDS
dc.subjectARYLTRIALKYLTINS
dc.subjectBORANE
dc.subjectORGANOTIN HYDRIDES
dc.subjectTRANSMETALLATIONS
dc.titleTransmetallations between aryltrialkyltins and borane: Synthesis of arylboronic acids and organotin hydrides
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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