Remote C−H functionalization using radical translocating arylating groups
Selective remote functionalization of aliphatic C(sp3)−H bonds is highly challenging and often requires transition metals and/or directing groups. Here, the authors show the γ-arylation of aliphatic alcohols via a two-step radical translocation and subsequent radical aryl migration.
Enregistré dans:
Auteurs principaux: | Florian W. Friese, Christian Mück-Lichtenfeld, Armido Studer |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2018
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/c959adcc6ac248cb8f072d3ca84f24a4 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Benzylic C−H acylation by cooperative NHC and photoredox catalysis
par: Qing-Yuan Meng, et autres
Publié: (2021) -
Aryl radical-mediated N-heterocyclic carbene catalysis
par: Yuki Matsuki, et autres
Publié: (2021) -
The role of DNA-binding and ARNT dimerization on the nucleo-cytoplasmic translocation of the aryl hydrocarbon receptor
par: Rashad Haidar, et autres
Publié: (2021) -
Enantioselective benzylic C–H arylation via photoredox and nickel dual catalysis
par: Xiaokai Cheng, et autres
Publié: (2019) -
Thioketone-directed rhodium(I) catalyzed enantioselective C-H bond arylation of ferrocenes
par: Zhong-Jian Cai, et autres
Publié: (2019)