Cargando…
Highly selective nickel-catalyzed gem-difluoropropargylation of unactivated alkylzinc reagents
In spite of the important applications of difluoroalkylated molecules in medicinal chemistry, to date, the reaction of difluoroalkylating reagents with unactivated, aliphatic substrates through a controllable manner remains challenging and has not been reported. Here we describe an efficient nickel-...
Autores principales: | An, Lun, Xu, Chang, Zhang, Xingang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684216/ https://www.ncbi.nlm.nih.gov/pubmed/29133781 http://dx.doi.org/10.1038/s41467-017-01540-1 |
Ejemplares similares
-
Highly Selective Palladium-Catalyzed Cross-Coupling
of Secondary Alkylzinc Reagents with Heteroaryl Halides
por: Yang, Yang, et al.
Publicado: (2014) -
Salt-stabilized alkylzinc pivalates: versatile reagents for cobalt-catalyzed selective 1,2-dialkylation
por: Lin, Jie, et al.
Publicado: (2023) -
Cobalt‐Catalyzed Cross‐Coupling of Functionalized Alkylzinc Reagents with (Hetero)Aryl Halides
por: Lutter, Ferdinand H., et al.
Publicado: (2020) -
Synthesis of fluorinated δ-lactams via cycloisomerization of gem-difluoropropargyl amides
por: Arimitsu, Satoru, et al.
Publicado: (2010) -
Active template rotaxane synthesis through the Ni-catalyzed cross-coupling of alkylzinc reagents with redox-active esters
por: Echavarren, Javier, et al.
Publicado: (2019)