dc.contributorPaixão, Márcio Weber
dc.contributorhttp://lattes.cnpq.br/3773908504964104
dc.contributorhttp://lattes.cnpq.br/3123398279809365
dc.creatorSilva, Rodrigo César da
dc.date.accessioned2014-12-02
dc.date.accessioned2016-06-02T20:34:58Z
dc.date.available2014-12-02
dc.date.available2016-06-02T20:34:58Z
dc.date.created2014-12-02
dc.date.created2016-06-02T20:34:58Z
dc.date.issued2014-08-07
dc.identifierSILVA, Rodrigo César da. Conjugate addition reactions of indoles and oxindoles employing organocatalys. 2014. 204 f. Tese (Doutorado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2014.
dc.identifierhttps://repositorio.ufscar.br/handle/ufscar/6326
dc.description.abstractOrganocatalysis has emerged as a powerful synthetic tool which accelerated the development of new methods to obtain symmetric and asymmetric molecules. Furthermore, the use of small organic molecules such as amino acids derivatives, ureas, thioureas and squaramides are the leading characters in this area. In the present work, we designed a new class of organocatalysts, acting as hydrogen bond donors activation mode and subsequently catalytic activity was evaluated in the Michael addition type reactions of indoles to nitrostyrene. The synthetic route for obtaining the organocatalysts was extremely short, providing the product in just a single synthetic step in excellent yields. (CONTINUA...)
dc.publisherUniversidade Federal de São Carlos
dc.publisherBR
dc.publisherUFSCar
dc.publisherPrograma de Pós-Graduação em Química - PPGQ
dc.rightsAcesso Aberto
dc.subjectSíntese orgânica
dc.subjectOrganocatálise
dc.titleReações de adição conjugada de indóis e oxindóis empregando organocatálise
dc.typeTesis


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