Affiliation:
1. Chair of Inorganic Chemistry II Faculty of Chemistry and Biochemistry Ruhr-University Bochum Universitätsstr. 150 44801 Bochum Germany
Abstract
AbstractPalladium‐catalyzed coupling reactions of small nucleophiles are of great interest, but challenging due to difficulties in selectivity control. Herein, we report the development of a new platform of P,N‐ligands consisting of ylide‐functionalized phosphines with aminophosphonium groups (NYPhos) to address this challenge. These phosphine ligands are easily accessible in a wide structural diversity with highly modular electronic and steric properties. Based on a family of 14 ligands the selective monoarylation of acetone as well as other challenging ketones and amides was accomplished with record‐setting activities even for aryl chlorides at room temperature including late‐stage functionalizations of drug molecules. Moreover, ammonia and other small primary amines could be coupled at mild conditions. Isolation and structure analyses of palladium complexes within the catalytic cycle confirmed that the P,N‐coordination mode is necessary to achieve the observed selectivities. It also demonstrated the facile adjustability of the N‐donor strength, which is beneficial for the targeted design of tailored P,N‐ligands for future applications.
Funder
Deutsche Forschungsgemeinschaft
Verband der Chemischen Industrie