Liégault Benoît, Renaud Jean-Luc, Bruneau Christian
Sciences Chimiques de Rennes, UMR 6226, Catalyse et Organométalliques, Université de Rennes 1, Campus de Beaulieu, 35042 Rennes Cedex, France.
Chem Soc Rev. 2008 Feb;37(2):290-9. doi: 10.1039/b704255h. Epub 2007 Oct 17.
Palladium-catalyzed transformations of aryl halides and pseudo-halides involving carbonylation, carbon-carbon and carbon-heteroatom bond-forming reactions, etc. are very well documented, and have already been reviewed several times. The metal-catalyzed activation of benzylic derivatives is much less described. However, during the last decades, a number of papers have shown the interest offered by benzylic derivatives (halides, carbonates, acetates, phosphonates) in selective catalytic reactions for organic synthesis, most of them in the presence of palladium catalysts. The purpose of this tutorial review is to highlight selected examples of palladium-catalyzed transformations involving reactive benzylic derivatives.
钯催化的芳基卤化物和拟卤化物的转化反应,包括羰基化反应、碳-碳键和碳-杂原子键形成反应等,已有充分的文献记载,并且已经被多次综述。金属催化的苄基衍生物的活化反应则较少被描述。然而,在过去几十年中,许多论文表明苄基衍生物(卤化物、碳酸盐、乙酸盐、膦酸盐)在有机合成的选择性催化反应中具有吸引力,其中大多数反应是在钯催化剂存在下进行的。本教程综述的目的是突出钯催化的涉及活性苄基衍生物的转化反应的选定实例。