Cargando…
Pd-catalysed ligand-enabled carboxylate-directed highly regioselective arylation of aliphatic acids
α-amino acids bearing aromatic side chains are important synthetic units in the synthesis of peptides and natural products. Although various β-C-H arylation methodologies for amino acid derivatives involving the assistance of directing groups have been extensively developed, syntheses that directly...
Autores principales: | Zhu, Yan, Chen, Xiaolan, Yuan, Chunchen, Li, Guobao, Zhang, Jingyu, Zhao, Yingsheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384235/ https://www.ncbi.nlm.nih.gov/pubmed/28383026 http://dx.doi.org/10.1038/ncomms14904 |
Ejemplares similares
-
A Fluorinated
Ligand Enables Room-Temperature and
Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides
por: Sather, Aaron C., et al.
Publicado: (2015) -
Hindered aryl bromides for regioselective palladium-catalysed direct arylation at less favourable C5-carbon of 3-substituted thiophenes
por: Jin, Rongwei, et al.
Publicado: (2014) -
An umpolung-enabled copper-catalysed regioselective hydroamination approach to α-amino acids
por: Nishino, Soshi, et al.
Publicado: (2021) -
Challenging nickel-catalysed amine arylations enabled by tailored ancillary ligand design
por: Lavoie, Christopher M., et al.
Publicado: (2016) -
Pd-catalysed C–H functionalisation of free carboxylic acids
por: Dutta, Suparna, et al.
Publicado: (2022)