dc.creatorCunha, Silvio do Desterro
dc.creatorRodrigues Jr., Manoel T.
dc.creatorCunha, Silvio do Desterro
dc.creatorRodrigues Jr., Manoel T.
dc.date.accessioned2012-07-10T15:56:41Z
dc.date.accessioned2022-10-07T15:33:08Z
dc.date.available2012-07-10T15:56:41Z
dc.date.available2022-10-07T15:33:08Z
dc.date.created2012-07-10T15:56:41Z
dc.date.issued2006
dc.identifier0040-4039
dc.identifierhttp://www.repositorio.ufba.br/ri/handle/ri/6395
dc.identifierv.47, n.39
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4005340
dc.description.abstractThis work describes the first catalytic bismuth-promoted synthesis of polysubstituted guanidines in good yields through the guanylation reaction of N-benzoyl or N-phenylthioureas with primary and secondary amines, but now employing equimolar amounts of each organic reagent. Both bismuth iodine and bismuth nitrate were efficient as inorganic thiophiles at only 5 mol % in relation to substrates, being the first example of inorganic thiophiles acting in guanylation at catalytic levels
dc.languageen
dc.publisherTetrahedron Letters
dc.sourcehttp://dx.doi.org/10.1016/j.tetlet.2006.07.138
dc.titleThe first bismuth(III)-catalyzed guanylation of thioureas
dc.typeArtigo de Periódico


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