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Palladium-catalyzed borylation and Suzuki coupling (BSC) to obtain beta-substituted dehydroamino acid derivatives

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Detalhes bibliográficos
Resumo:Several benzo[b]thienyldehydroamino acids were prepared by one pot palladium-catalyzed borylation and Suzuki coupling (BSC) from bromobenzo[b]thiophenes containing EDG (OMe or Me), as the component to be borylated with pinacolborane, and pure stereoisomers of beta-bromodehydroamino acid derivatives. To our knowledge it is the first time that the BSC reaction involves a non aromatic system.
Autores principais:Abreu, Ana S.
Outros Autores:Silva, Natália O.; Ferreira, Paula M. T.; Queiroz, Maria João R. P.
Assunto:Benzo[b]thiophenes Borylation Palladium Suzuki coupling Dehydroamino acids
Ano:2003
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
Descrição
Resumo:Several benzo[b]thienyldehydroamino acids were prepared by one pot palladium-catalyzed borylation and Suzuki coupling (BSC) from bromobenzo[b]thiophenes containing EDG (OMe or Me), as the component to be borylated with pinacolborane, and pure stereoisomers of beta-bromodehydroamino acid derivatives. To our knowledge it is the first time that the BSC reaction involves a non aromatic system.

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