Laboratory of Organic Synthesis Bio- and Organocatalysis, Chemistry Department, Universidad de los Andes, Cra. 1 No 18A-12 Q:305, Bogotá 111711, Colombia.
Molecules. 2018 Sep 18;23(9):2382. doi: 10.3390/molecules23092382.
Amides are undeniably some of the most important compounds in Nature and the chemical industry, being present in biomolecules, materials, pharmaceuticals and many other substances. Unfortunately, the traditional synthesis of amides suffers from some important drawbacks, principally the use of stoichiometric activators or the need to use highly reactive carboxylic acid derivatives. In recent years, the transamidation reaction has emerged as a valuable alternative to prepare amides. The reactivity of amides makes their direct reaction with nitrogen nucleophiles difficult; thus, the direct transamidation reaction needs a catalyst in order to activate the amide moiety and to promote the completion of the reaction because equilibrium is established. In this review, we present research on direct transamidation reactions ranging from studies of the mechanism to the recent developments of more applicable and versatile methodologies, emphasizing those reactions involving activation with metal catalysts.
酰胺无疑是自然界和化学工业中最重要的化合物之一,存在于生物分子、材料、药物和许多其他物质中。不幸的是,酰胺的传统合成方法存在一些重要的缺点,主要是使用化学计量的活化剂或需要使用高反应性的羧酸衍生物。近年来,转酰胺反应作为一种有价值的替代方法来制备酰胺。酰胺的反应性使得它们与氮亲核试剂的直接反应变得困难;因此,直接转酰胺反应需要催化剂来激活酰胺部分,并促进反应的完成,因为平衡是建立的。在这篇综述中,我们介绍了直接转酰胺反应的研究,从机理研究到更适用和通用的方法学的最新进展,强调了那些涉及金属催化剂活化的反应。