dc.contributor | Paixão, Márcio Weber | |
dc.contributor | http://lattes.cnpq.br/3773908504964104 | |
dc.contributor | http://lattes.cnpq.br/3123398279809365 | |
dc.creator | Silva, Rodrigo César da | |
dc.date.accessioned | 2014-12-02 | |
dc.date.accessioned | 2016-06-02T20:34:58Z | |
dc.date.available | 2014-12-02 | |
dc.date.available | 2016-06-02T20:34:58Z | |
dc.date.created | 2014-12-02 | |
dc.date.created | 2016-06-02T20:34:58Z | |
dc.date.issued | 2014-08-07 | |
dc.identifier | SILVA, 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.identifier | https://repositorio.ufscar.br/handle/ufscar/6326 | |
dc.description.abstract | Organocatalysis 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.publisher | Universidade Federal de São Carlos | |
dc.publisher | BR | |
dc.publisher | UFSCar | |
dc.publisher | Programa de Pós-Graduação em Química - PPGQ | |
dc.rights | Acesso Aberto | |
dc.subject | Síntese orgânica | |
dc.subject | Organocatálise | |
dc.title | Reações de adição conjugada de indóis e oxindóis empregando organocatálise | |
dc.type | Tesis | |