Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149, Münster, Germany.
Angew Chem Int Ed Engl. 2019 Jul 29;58(31):10460-10476. doi: 10.1002/anie.201814471. Epub 2019 Apr 29.
Arene hydrogenation provides direct access to saturated carbo- and heterocycles and thus its strategic application may be used to shorten synthetic routes. This powerful transformation is widely applied in industry and is expected to facilitate major breakthroughs in the applied sciences. The ability to overcome aromaticity while controlling diastereo-, enantio-, and chemoselectivity is central to the use of hydrogenation in the preparation of complex molecules. In general, the hydrogenation of multisubstituted arenes yields predominantly the cis isomer. Enantiocontrol is imparted by chiral auxiliaries, Brønsted acids, or transition-metal catalysts. Recent studies have demonstrated that highly chemoselective transformations are possible. Such methods and the underlying strategies are reviewed herein, with an emphasis on synthetically useful examples that employ readily available catalysts.
芳环加氢提供了直接构建饱和碳环和杂环化合物的途径,因此其在合成中的战略应用可以缩短合成路线。这种强大的转化在工业中得到了广泛应用,并有望在应用科学中取得重大突破。克服芳香性的同时控制非对映选择性、对映选择性和化学选择性是在复杂分子的制备中应用加氢的关键。一般来说,多取代芳环的加氢主要生成顺式异构体。手性助剂、布朗斯台德酸或过渡金属催化剂赋予对映选择性。最近的研究表明,高度选择性的转化是可能的。本文综述了这些方法和基础策略,重点介绍了使用易得催化剂的具有合成实用性的例子。