An unusual endo-selective C-H hydroarylationof norbornene by the Rh(I)-catalyzed reactionof benzamides
Investigating unusual organometallic pathways may help to efficiently control product selectivity in homogeneous catalysis. Here, the authors report the hydroarylation of aromatic amides with norbornene derivatives and propose the formation of a rhodium-carbene intermediate leading to rarely observe...
Guardado en:
Autores principales: | Kaname Shibata, Satoko Natsui, Mamoru Tobisu, Yoshiya Fukumoto, Naoto Chatani |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/fe975581af0e40b3840956db9500644a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Chromium-catalyzed para-selective formation of quaternary carbon centers by alkylation of benzamide derivatives
por: Pei Liu, et al.
Publicado: (2018) -
Sulfenamide-enabled ortho thiolation of aryl iodides via palladium/norbornene cooperative catalysis
por: Renhe Li, et al.
Publicado: (2019) -
Switching polymorph stabilities with impurities provides a thermodynamic route to benzamide form III
por: Weronika Kras, et al.
Publicado: (2021) -
BENZAMIDE DERIVATIVES AS POTENTIAL CANDIDATES FOR ANTI-ALZHEIMER, ANTI-FATIGUE, ANTI-UREASE AND ANTI-OXIDANT ACTIVITY
por: TAJ,M. B, et al.
Publicado: (2017) -
Direct alkylation of N,N-dialkyl benzamides with methyl sulfides under transition metal-free conditions
por: Can-Can Bao, et al.
Publicado: (2021)