Löffler Julian, Kaiser Nicolas, Knyszek Daniel, Krischer Felix, Jörges Mike, Feichtner Kai-Stephan, Gessner Viktoria H
Chair of Inorganic Chemistry II, Faculty of Chemistry and Biochemistry, Ruhr-University Bochum, Universitätsstr. 150, 44801, Bochum, Germany.
Angew Chem Int Ed Engl. 2024 Sep 2;63(36):e202408947. doi: 10.1002/anie.202408947. Epub 2024 Aug 2.
Palladium-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.
钯催化的小分子亲核试剂的偶联反应备受关注,但由于选择性控制困难而具有挑战性。在此,我们报道了一种由具有氨基鏻基团的叶立德功能化膦组成的新型P,N配体平台的开发,以应对这一挑战。这些膦配体易于获得,具有广泛的结构多样性以及高度模块化的电子和空间性质。基于14种配体的系列,即使对于芳基氯化物,在室温下也能以创纪录的活性实现丙酮以及其他具有挑战性的酮和酰胺的选择性单芳基化,包括药物分子的后期功能化。此外,氨和其他小分子伯胺可以在温和条件下进行偶联。催化循环中钯配合物的分离和结构分析证实,P,N配位模式对于实现所观察到的选择性是必要的。它还证明了氮供体强度的易于调节性,这有利于为未来应用量身定制P,N配体的靶向设计。