Mechanisms in Iodine Catalysis

被引:163
作者
Breugst, Martin [1 ]
von der Heiden, Daniel [1 ]
机构
[1] Univ Cologne, Dept Chem, Greinstr 4, D-50939 Cologne, Germany
关键词
Bronsted acids; halogen bonding; iodine catalysis; Lewis acids; reaction mechanisms; DIELS-ALDER REACTION; ORGANIC DIVALENT SULFUR; SOLVENT-FREE CONDITIONS; ELECTRON-DEFICIENT OLEFINS; MUKAIYAMA ALDOL REACTIONS; AZA-PRINS CYCLIZATION; +1 OXIDATION-STATE; ONE-POT SYNTHESIS; MOLECULAR-IODINE; CARBONYL-COMPOUNDS;
D O I
10.1002/chem.201706136
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 BrOnsted 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.
引用
收藏
页码:9187 / 9199
页数:13
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