dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorStefani, Helio A. [UNIFESP]
dc.creatorGuadagnin, Rafael C.
dc.creatorKeppler, Artur F.
dc.creatorBotteselle, Giancarlo V.
dc.creatorComasseto, Joao V.
dc.creatorSuganuma, Carlos A.
dc.date.accessioned2016-01-24T13:49:34Z
dc.date.accessioned2023-09-04T18:29:16Z
dc.date.available2016-01-24T13:49:34Z
dc.date.available2023-09-04T18:29:16Z
dc.date.created2016-01-24T13:49:34Z
dc.date.issued2008-02-05
dc.identifierBeilstein Journal of Organic Chemistry. Frankfurt Am Main: Beilstein-institut, v. 4, 4 p., 2008.
dc.identifier1860-5397
dc.identifierhttp://repositorio.unifesp.br/handle/11600/30442
dc.identifierWOS000253207700001.pdf
dc.identifier10.1186/1860-5397-4-9
dc.identifierWOS:000253207700001
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8615249
dc.description.abstractThrough direct transmetalation reaction of Z-vinylic tellurides with nBuLi was observed the unexpected isomerization of double bonds leading to potassium E-vinyltrifluoroborates salts in low to moderate yields. Using EPR spin trapping experiments the radical species that promoted the stereoinversion of Z-vinylic organometallic species during the preparation of potassium vinyltrifluoroborate salts was identified. the experiments support the proposed mechanism, which is based on the homolytic cleavage of the TenBu bond.
dc.languageeng
dc.publisherBeilstein-institut
dc.relationBeilstein Journal of Organic Chemistry
dc.rightsAcesso aberto
dc.titleMechanistic aspects of the isomerization of Z-vinylic tellurides double bonds in the synthesis of potassium Z-vinyltrifluoroborate salts
dc.typeArtigo


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