Cargando…
Transition-metal-free allylation of 2-azaallyls with allyl ethers through polar and radical mechanisms
Allylation of nucleophiles with highly reactive electrophiles like allyl halides can be conducted without metal catalysts. Less reactive electrophiles, such as allyl esters and carbonates, usually require a transition metal catalyst to facilitate the allylation. Herein, we report a unique transition...
Autores principales: | Deng, Guogang, Duan, Shengzu, Wang, Jing, Chen, Zhuo, Liu, Tongqi, Chen, Wen, Zhang, Hongbin, Yang, Xiaodong, Walsh, Patrick J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222226/ https://www.ncbi.nlm.nih.gov/pubmed/34162867 http://dx.doi.org/10.1038/s41467-021-24027-6 |
Ejemplares similares
-
Nickel-catalyzed enantioselective vinylation of aryl 2-azaallyl anions
por: Duan, Shengzu, et al.
Publicado: (2021) -
α-Branched amines through radical coupling with 2-azaallyl anions, redox active esters and alkenes
por: Duan, Shengzu, et al.
Publicado: (2022) -
Carboxylate-directed C–H allylation with allyl alcohols or ethers
por: Hu, Xiao-Qiang, et al.
Publicado: (2018) -
Transition‐Metal‐Free Borylation of Allylic and Propargylic Alcohols
por: Miralles, Núria, et al.
Publicado: (2016) -
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
por: Panetti, Grace B., et al.
Publicado: (2021)