Chemodivergent assembly of ortho-functionalized phenols with tunable selectivity via rhodium(III)-catalyzed and solvent-controlled C-H activation
Ortho functionalisation of phenols can be achieved using N-phenoxy amide directing groups. Here a method for chemodivergent C-H alkenylation, alkylation, carboetherification, or [3 + 2] annulation is presented, with product selectivity determined by the choice of solvent.
Guardado en:
Autores principales: | Haiman Zhang, Shuang Lin, Hui Gao, Kaixin Zhang, Yi Wang, Zhi Zhou, Wei Yi |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/5c42cf4a39ce47299fc463dd179e42df |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Chemodivergent manganese-catalyzed C–H activation: modular synthesis of fluorogenic probes
por: Nikolaos Kaplaneris, et al.
Publicado: (2021) -
A bioinspired and biocompatible ortho-sulfiliminyl phenol synthesis
por: Feng Xiong, et al.
Publicado: (2017) -
Divergent rhodium-catalyzed electrochemical vinylic C–H annulation of acrylamides with alkynes
por: Yi-Kang Xing, et al.
Publicado: (2021) -
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation
por: Cai You, et al.
Publicado: (2018) -
Thioketone-directed rhodium(I) catalyzed enantioselective C-H bond arylation of ferrocenes
por: Zhong-Jian Cai, et al.
Publicado: (2019)