Implications of Active Intermediate and Olefin Attachment Position in the Piperine Metathesis
Carregando...
Arquivos
Fontes externas
Fontes externas
Data
Orientador
Coorientador
Pós-graduação
Curso de graduação
Título da Revista
ISSN da Revista
Título de Volume
Editor
Tipo
Artigo
Direito de acesso
Arquivos
Fontes externas
Fontes externas
Resumo
Abstract: First and second generation of Grubbs catalysts (G1 and G2) were applied in the piperine olefin metathesis under different conditions. G1 was used in self-metathesis, G2 was implemented in both, self and cross-metathesis of piperine with eugenol. Results allowed to implicate about the main intermediate of the reaction and the position of olefin attachment to the catalyst, assuming that the reaction follows a pathway where 2A=B olefin leads to the formation of A=A and B=B. In addition, the results contributed to the studies of catalyst’s reactivity when the olefin metathesis product required the high electronic effect of the N-heterocyclic of G2. In this paper, the highest activity of G2 in the olefin metathesis of eugenol was observed when the first intermediate was Ru-eugenol-moiety in the cross-metathesis of the piperine with eugenol. This demonstrates that the acidity of the new carbene in the intermediate species causes inactivity only in the reaction with piperine.
Descrição
Palavras-chave
active species, metathesis reaction, piperine, ruthenium
Idioma
Inglês
Citação
Kinetics and Catalysis, v. 64, n. 6, p. 783-792, 2023.




