Microwave-Assisted Heck Arylations of Non-Activated N-Acyl-3-pyrrolines with Arenediazonium Tetrafluoroborates
AUTOR(ES)
Finelli, Fernanda G., Godoi, Marla N., Correia, Carlos R. D.
FONTE
J. Braz. Chem. Soc.
DATA DE PUBLICAÇÃO
2015-05
RESUMO
Successful Heck-Matsuda arylations of non-activated olefins applying microwave irradiation as an alternative heating mode are presented. Cleaner reactions were performed with arenediazonium tetrafluoroborates bearing electron-donating and electron-withdrawing groups in good to excellent yields with reaction times reduced from 3.5-18 h to 12-30 min.
Documentos Relacionados
- Microwave-assisted reaction of 2,3-dichloronaphthoquinone with aminopyridines
- Microwave-assisted synthesis of Nitroketene N,S-Arylaminoacetals
- Microwave-assisted rapid deprotection of oligodeoxyribonucleotides.
- Conventional and microwave-assisted reaction of N-hydroxymethylphthalimide with arylamines: synthesis of N-(arylaminomethyl)-phthalimides
- Microwave-assisted rapid and regioselective synthesis of N-(alkoxycarbonylmethyl) nucleobases in water