Síntese de novas azocinas diversamente funcionalizadas

Detalhes bibliográficos
Ano de defesa: 2013
Autor(a) principal: Laureana Fonseca Lanna Marinho
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Minas Gerais
UFMG
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/1843/SFSA-96PSG2
Resumo: This work is divided into four parts. The first part presents the synthesis of chiral azocines (eight-membered nitrogen heterocycles) by a cycloaddition [2 +2] between tetrahydropyridines (THPs) and ethylpropiolate. The chiral THPs were synthesized from chiral pyridinium salts, which were obtained through Zincke reaction. This strategy gave chiral azocines containing a chiral inductor directly linked to the nitrogen atom. These azocine derivatives were converted in their respective iminium salts by treatment with methanesulfonic acid. These salts were usedfor studies of regioselectivity in nucleophilic addition reactions.The second part of this dissertation shows the attempts to optimize the reaction of iminium ions formation of from achiral azocines as well as the use of these compounds to obtain new products. The iminium salts synthesized were treated with different nucleophiles (sodiumazide and sodium phenolate) to produce some new addition products.The third part describes the synthesis of novel achiral azocine triazole derivatives using a "click" reaction between an 6-azide-azocine and commercial or synthetized alkynes. In this part, four new triazole azocine compounds were obtained. Finally, some preliminary results on the effect of obtained azocines as inhibitors of cholinesterases are presented. The azocine derivatives were tested and did not inhibit the acetylcholinesterase enzyme (AChE), known as an important approach to treat patients with Alzheimer´s disease.