Department of Chemistry, University of Cologne, Greinstraße 4, 50939, Köln, Germany.
Chemistry. 2018 Jul 2;24(37):9187-9199. doi: 10.1002/chem.201706136. Epub 2018 Apr 30.
Molecular iodine has been used for more than 100 years as a remarkable catalyst for many organic transformations such as cycloadditions, Michael and aldol reactions, or esterifications. Different explanations for the origin of its catalytic effect have been proposed in the last decades including a "hidden" Brønsted acid catalysis by HI, a Lewis-acid (or halogen-bond) activation, or catalysis by an iodonium(I) species. Recently, iodine catalysis again gained more interest due to the latest developments in halogen-bond catalysis. In this Minireview, we first summarize the experimental basis for the proposed modes of activation. Subsequently, we analyze typical iodine-catalyzed reactions to gain more insights into the underlying reaction mechanisms.
分子碘作为一种显著的催化剂,已经被应用了 100 多年,用于许多有机转化反应,如环加成、迈克尔和Aldol 反应,或酯化反应。在过去的几十年中,人们提出了不同的解释来阐明其催化作用的起源,包括 HI 的“隐藏”Brønsted 酸催化、Lewis 酸(或卤素键)活化,或碘鎓(I)物种的催化。最近,由于卤键催化的最新发展,碘催化再次引起了更多的关注。在这篇综述中,我们首先总结了所提出的活化模式的实验基础。随后,我们分析了典型的碘催化反应,以深入了解潜在的反应机制。