NH2 as a directing group: from the unexpected cyclopalladation of aminoesters to the preparation of benzolactams by Pd(II)-catalyzed carbonylation of N-unprotected arylethylamines

An unusual NH2-directed Pd(II)-catalytic carbonylation of quaternary aromatic α-amino esters to yield benzolactams has been developed. The steric hindrance around the amino group is pivotal for the success of the process. The stoichiometric cyclometallation of a variety amino esters has been studied...

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Detalhes bibliográficos
Autores: Albert Mach, Joan, Ariza Piquer, Xavier, Calvet Pallàs, Maria Teresa, Font Bardia, Ma. Mercedes, García Gómez, Jordi, Granell Sanvicente, Jaime Ramón, Lamela, Andrea, López Barallobre, Blanca, Martínez López, Manuel, 1957-, Ortega, Laura, Rodríguez Ramírez, Aleix, Santos, David
Tipo de documento: artigo
Estado:Versión aceptada para publicación
Data de publicação:2013
País:España
Recursos:Universidad de Barcelona
Repositório:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/43589
Acesso em linha:https://hdl.handle.net/2445/43589
Access Level:Acceso aberto
Palavra-chave:Pal·ladi (Element químic)
Cinètica química
Compostos organometàl·lics
Cristal·lografia
Catàlisi
Palladium
Chemical kinetics
Organometallic compounds
Crystallography
Catalysis
Descrição
Resumo:An unusual NH2-directed Pd(II)-catalytic carbonylation of quaternary aromatic α-amino esters to yield benzolactams has been developed. The steric hindrance around the amino group is pivotal for the success of the process. The stoichiometric cyclometallation of a variety amino esters has been studied in order to evaluate the influence of the different variables (size of the metallacycle, aromatic ring substituents, and steric bulk) in the process, and a complete kinetico-mechanistic study of the cyclopalladation process has been carried out. The experimental results indicate that the full substitution of the carbon in the α position of the amino esters plays an important role in their cyclopalladation reaction. The reaction shows a strong bias to 6-membered lactams over the 5-membered analogues, which can be explained by a greater reactivity of the six-membered palladacycles.