Melchiorre Paolo, Marigo Mauro, Carlone Armando, Bartoli Giuseppe
Department of Organic Chemistry A. Mangini, Alma Mater Studiorum-Università di Bologna, Viale Risorgimento 4, 40136 Bologna, Italy.
Angew Chem Int Ed Engl. 2008;47(33):6138-71. doi: 10.1002/anie.200705523.
Catalysis with chiral secondary amines (asymmetric aminocatalysis) has become a well-established and powerful synthetic tool for the chemo- and enantioselective functionalization of carbonyl compounds. In the last eight years alone, this field has grown at such an extraordinary pace that it is now recognized as an independent area of synthetic chemistry, where the goal is the preparation of any chiral molecule in an efficient, rapid, and stereoselective manner. This has been made possible by the impressive level of scientific competition and high quality research generated in this area. This Review describes this "Asymmetric Aminocatalysis Gold Rush" and charts the milestones in its development. As in all areas of science, progress depends on human effort.
使用手性仲胺进行催化(不对称胺催化)已成为一种成熟且强大的合成工具,用于羰基化合物的化学选择性和对映选择性官能化。仅在过去八年中,该领域就以惊人的速度发展,如今已被公认为合成化学的一个独立领域,其目标是以高效、快速和立体选择性的方式制备任何手性分子。这得益于该领域产生的令人瞩目的科学竞争水平和高质量研究。本综述描述了这场“不对称胺催化淘金热”,并梳理了其发展历程中的里程碑。与所有科学领域一样,进步取决于人类的努力。