Metátese de fechamento de anéis de derivados da R-(-)- Carvona

Detalhes bibliográficos
Ano de defesa: 2012
Autor(a) principal: Desiderá, André Luiz
Orientador(a): Brocksom, Timothy John lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Carlos
Programa de Pós-Graduação: Programa de Pós-Graduação em Química - PPGQ
Departamento: Não Informado pela instituição
País: BR
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufscar.br/handle/20.500.14289/6549
Resumo: In this work was developed a new synthetic route to obtain cicloeptenone not conjugated selectively, through a faster and simpler methodology, and in accordance with good practices of green chemistry. By experimental techniques of nuclear magnetic ressonance (NMR) were assigned the stereochemistry of two diastereoisomeric pairs. Intermediate compounds were synthesized for the synthesis of sesquiterpenes guaianes (a), nor-guaianes (b) and pseudo-guaianes (c). To react the mono-allylated to form bis-alilados products with and without replacement, for further formation of compounds containing ring-type spiro[4.6]undecane. It was also developed a new methodology for formation of tensioned spiro rings (d) derivatives from (R)-carvone, using the reaction of ring closure metathesis. Using this methodology allylation, obtained was a precursor for a new way to reach the system bicyclo [5.3.0] decane (e). In total, 18 compounds were synthesized, of which 7 are unpublished.