Alma Mater Studiorum-University of Bologna, Department of Chemistry G. Ciamician, via Selmi 2, Bologna 40126, Italien.
Angew Chem Int Ed Engl. 2009;48(51):9608-44. doi: 10.1002/anie.200901843.
140 years ago Adolf von Baeyer proposed the structure of a heteroaromatic compound which revolutionized organic and medical chemistry: indole. After more than a century, indole itself and the complexity of naturally occurring indole derivatives continue to inspire and influence developments in synthetic chemistry. In particular, the ubiquitous presence of indole rings in pharmaceuticals, agrochemicals, and functional materials are testament to the ever increasing interest in the design of mild and efficient synthetic routes to functionalized indole derivatives. This Review emphasizes the achievements in the selective catalytic functionalization of indoles (C-C bond-forming processes) over the last four years.
140 年前,阿道夫·冯·拜尔提出了一种杂环化合物的结构,这一结构彻底改变了有机和医学化学:吲哚。一个多世纪后,吲哚本身及其复杂的天然吲哚衍生物继续激发和影响合成化学的发展。特别是,在药物、农用化学品和功能材料中无处不在的吲哚环证明了人们对设计温和高效的合成路线来制备功能化吲哚衍生物的兴趣日益增加。本文综述了过去四年中吲哚选择性催化功能化(C-C 键形成过程)方面的成就。