dc.contributorRicardo Jose Alves
dc.contributorRenata Barbosa de Oliveira
dc.contributorAngelo de Fatima
dc.creatorMagno Carvalho Pires
dc.date.accessioned2019-08-12T12:39:52Z
dc.date.accessioned2022-10-03T23:30:35Z
dc.date.available2019-08-12T12:39:52Z
dc.date.available2022-10-03T23:30:35Z
dc.date.created2019-08-12T12:39:52Z
dc.date.issued2009-07-24
dc.identifierhttp://hdl.handle.net/1843/FARD-82KM3T
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3823733
dc.description.abstractThe macrocycles form an important class of compounds that, by having various biological activities and many drugs available, are targets of intense research. The challenge of synthesizing macrocycles via short and efficient synthetic routes, with yields that made possible the assessment of organic compounds, were the goals of this work.Two glycosides were synthesized from D-glucosamine by four steps. These glycosides were submitted to Bu3SnH/AIBN-mediated radical carbocyclization reactions to furnish three macrocycles and two products of aromatic radical substitution.
dc.publisherUniversidade Federal de Minas Gerais
dc.publisherUFMG
dc.rightsAcesso Aberto
dc.subjectmacrociclos
dc.subjectciclização radicalar
dc.subjectCarboidratos
dc.subjectglicosamina
dc.titleSíntese de macrociclos derivados de D-glicosamina.
dc.typeDissertação de Mestrado


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