Preparation of benzolactams by Pd(II)-catalyzed carbonylation of N-unprotected arylethylamines


Autoria(s): López, Blanca; Rodríguez Ramírez, Aleix; Santos, David; Albert Mach, Joan; Ariza Piquer, Xavier; García Gómez, Jordi; Granell Sanvicente, Jaime Ramón
Contribuinte(s)

Universitat de Barcelona

Resumo

An unprecedented NH2-directed Pd(II)-catalytic carbonylation of quaternary aromatic α -amino esters to yield 6-membered 10 benzolactams has been developed. The reaction shows a strong bias to 6-membered lactams over 5-membered ones. The steric hindrance around the amino group seems to be pivotal for the success of the process.

Identificador

http://hdl.handle.net/2445/48695

Idioma(s)

eng

Publicador

Royal Society of Chemistry

Direitos

(c) López, Blanca et al., 2011

info:eu-repo/semantics/openAccess

Palavras-Chave #Pal·ladi (Element químic) #Química organometàl·lica #Reaccions químiques #Lactames #Imines #Palladium #Organometallic chemistry #Chemical reactions #Lactams #Imines
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/acceptedVersion