Department of Chemistry , University of Wisconsin-Madison , 1101 University Avenue , Madison , Wisconsin 53706 , United States.
Chem Rev. 2018 Mar 14;118(5):2636-2679. doi: 10.1021/acs.chemrev.7b00334. Epub 2017 Oct 4.
Palladium-catalyzed aerobic oxidation reactions have been the focus of industrial application and extensive research efforts for nearly 60 years. A significant transition occurred in this field approximately 20 years ago, with the introduction of catalysts supported by ancillary ligands. The ligands play crucial roles in the reactions, including promotion of direct oxidation of palladium(0) by O, bypassing the typical requirement for Cu salts or related redox cocatalysts to facilitate oxidation of the reduced Pd catalyst; facilitation of key bond-breaking and bond-forming steps during substrate oxidation; and modulation of chemo-, regio-, or stereoselectivity of a reaction. The use of ligands has contributed to significant expansion of the scope of accessible aerobic oxidation reactions. Increased understanding of the role of ancillary ligands should promote the development of new synthetic transformations, enable improved control over the reaction selectivity, and improve catalyst activity and stability. This review surveys the different ligands that have been used to support palladium-catalyzed aerobic oxidation reactions and, where possible, describes mechanistic insights into the role played by the ancillary ligand.
钯催化的有氧氧化反应已经成为工业应用和广泛研究的焦点近 60 年。大约 20 年前,这个领域发生了重大转变,出现了由辅助配体支持的催化剂。这些配体在反应中起着至关重要的作用,包括促进钯(0)的直接氧化,绕过典型的需要铜盐或相关氧化还原助催化剂来促进还原的 Pd 催化剂的氧化;促进底物氧化过程中关键的键断裂和键形成步骤;调节反应的化学选择性、区域选择性或立体选择性。配体的使用促进了可进行的有氧氧化反应范围的显著扩大。对辅助配体作用的深入了解应该会促进新的合成转化的发展,能够更好地控制反应选择性,并提高催化剂的活性和稳定性。这篇综述调查了用于支持钯催化的有氧氧化反应的不同配体,并在可能的情况下,描述了对辅助配体所起作用的机制见解。