Cargando…
Tuning the reactivity of alkoxyl radicals from 1,5-hydrogen atom transfer to 1,2-silyl transfer
Controlling the reactivity of reactive intermediates is essential to achieve selective transformations. Due to the facile 1,5-hydrogen atom transfer (HAT), alkoxyl radicals have been proven to be important synthetic intermediates for the δ-functionalization of alcohols. Herein, we disclose a strateg...
Autores principales: | Yang, Zhaoliang, Niu, Yunhong, He, Xiaoqian, Chen, Suo, Liu, Shanshan, Li, Zhengyu, Chen, Xiang, Zhang, Yunxiao, Lan, Yu, Shen, Xiao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035221/ https://www.ncbi.nlm.nih.gov/pubmed/33837201 http://dx.doi.org/10.1038/s41467-021-22382-y |
Ejemplares similares
-
FLP‐Catalyzed Transfer Hydrogenation of Silyl Enol Ethers
por: Khan, Imtiaz, et al.
Publicado: (2018) -
Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
por: Papadakis, Raffaello, et al.
Publicado: (2016) -
Radical cascade synthesis of azoles via tandem hydrogen atom transfer
por: Chen, Andrew D., et al.
Publicado: (2020) -
Alcohols as Substrates and Solvents for the Construction of 3-Alkoxylated-2-Oxindoles by Direct Alkoxylation of 3-Halooxindoles
por: Lin, Bing, et al.
Publicado: (2017) -
Cobalt-catalyzed peri-selective alkoxylation of 1-naphthylamine derivatives
por: Han, Jiao-Na, et al.
Publicado: (2018)