Spatial Anion Control on Palladium for Mild C–H Arylation of Arenes
- 30 October 2020
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 142 (45) , 19040-19046
Abstract
C–H arylation of arenes without the use of directing groups is a challenge, even for simple molecules, such as benzene. We describe spatial anion control as a concept for the design of catalytic sites for C–H bond activation, thereby enabling nondirected C–H arylation of arenes at ambient temperature. The mild conditions enable late-stage structural diversification of biologically relevant small molecules, and site-selectivity complementary to that obtained with other methods of arene functionalization can be achieved. These results reveal the potential of spatial anion control in transition-metal catalysis for the functionalization of C–H bonds under mild conditions.Keywords
Funding Information
- China Scholarship Council
- Universit?t Z?rich
- Holcim Stiftung
This publication has 68 references indexed in Scilit:
- Recent Advances in C–H Activation for the Synthesis of π-Extended MaterialsACS Materials Letters, 2020
- Dual Ligand-Enabled Nondirected C–H Cyanation of ArenesACS Catalysis, 2019
- Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the FutureOrganometallics, 2018
- Ligand‐Promoted Non‐Directed C−H Cyanation of ArenesChemistry – A European Journal, 2018
- Recent applications of C–H functionalization in complex natural product synthesisChemical Society Reviews, 2018
- Dual Ligand‐Enabled Nondirected C−H Olefination of ArenesAngewandte Chemie International Edition, 2018
- Ligand-accelerated non-directed C–H functionalization of arenesNature, 2017
- The medicinal chemist's toolbox for late stage functionalization of drug-like moleculesChemical Society Reviews, 2015
- Recent developments in natural product synthesis using metal-catalysed C–H bond functionalisationChemical Society Reviews, 2011
- C−H Activation for the Construction of C−B BondsChemical Reviews, 2009