Zhu Yawei, Yang Shiyi, Zhou Tongliang, Szostak Michal
Department of Chemistry, Rutgers University, 73 Warren Street, Newark, New Jersey 07102, United States.
J Org Chem. 2024 Nov 15;89(22):16203-16213. doi: 10.1021/acs.joc.4c00103. Epub 2024 Jul 1.
In the past eight years, the selective cross-coupling of amides by N-C(O) bond activation has emerged as a highly attractive manifold for the manipulation of traditionally unreactive amide bonds. In this Special Issue on Next-Generation Cross-Coupling Chemistry, we report the Suzuki-Miyaura and Buchwald-Hartwig cross-coupling of amides by selective N-C(O) cleavage catalyzed by bench-stable, well-defined carboxylate Pd(II)-NHC (NHC = N-heterocyclic carbene) catalysts {[(NHC)Pd(OCR)]}. This class of Pd(II)-NHCs promotes cross-coupling under exceedingly mild room-temperature conditions owing to the facile dissociation of the carboxylate ligands to form the active complex. These readily accessible Pd(II)-NHC precatalysts show excellent functional group tolerance and are compatible with a broad range of amide activating groups. Considering the mild conditions for the cross-coupling and the facile access to carboxylate Pd(II)-NHC complexes, we anticipate that this class of bench-stable complexes will find wide application in the activation of amide N-C(O) and related acyl X-C(O) bonds.
在过去八年中,通过N-C(O)键活化实现的酰胺选择性交叉偶联已成为一种极具吸引力的方法,用于操控传统上无反应性的酰胺键。在本期关于下一代交叉偶联化学的特刊中,我们报道了由稳定、明确的羧酸盐钯(II)-氮杂环卡宾(NHC = N-杂环卡宾)催化剂{[(NHC)Pd(OCR)]}催化的酰胺通过选择性N-C(O)裂解实现的铃木-宫浦交叉偶联和布赫瓦尔德-哈特维希交叉偶联。由于羧酸盐配体易于解离形成活性络合物,这类钯(II)-NHC在极其温和的室温条件下促进交叉偶联。这些易于获得的钯(II)-NHC预催化剂表现出优异的官能团耐受性,并且与广泛的酰胺活化基团兼容。考虑到交叉偶联的温和条件以及易于获得羧酸盐钯(II)-NHC络合物,我们预计这类稳定的络合物将在酰胺N-C(O)和相关酰基X-C(O)键的活化中得到广泛应用。