Ryabchuk Pavel, Leischner Thomas, Kreyenschulte Carsten, Spannenberg Anke, Junge Kathrin, Beller Matthias
Leibniz-Institut für Katalyse e. V., Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
Angew Chem Int Ed Engl. 2020 Oct 12;59(42):18679-18685. doi: 10.1002/anie.202007613. Epub 2020 Aug 31.
A bifunctional 3d-metal catalyst for the cascade synthesis of diverse pyrroles from nitroarenes is presented. The optimal catalytic system Co/NGr-C@SiO -L is obtained by pyrolysis of a cobalt-impregnated composite followed by subsequent selective leaching. In the presence of this material, (transfer) hydrogenation of easily available nitroarenes and subsequent Paal-Knorr/Clauson-Kass condensation provides >40 pyrroles in good to high yields using dihydrogen, formic acid, or a CO/H O mixture (WGSR conditions) as reductant. In addition to the favorable step economy, this straightforward domino process does not require any solvents or external co-catalysts. The general synthetic utility of this methodology was demonstrated on a variety of functionalized substrates including the preparation of biologically active and pharmaceutically relevant compounds, for example, (+)-Isamoltane.
本文介绍了一种用于从硝基芳烃级联合成多种吡咯的双功能3D金属催化剂。通过对负载钴的复合材料进行热解,随后进行选择性浸出,得到了最佳催化体系Co/NGr-C@SiO -L。在这种材料存在的情况下,利用易于获得的硝基芳烃的(转移)氢化反应以及随后的帕尔-克诺尔/克劳森-卡斯缩合反应,以氢气、甲酸或CO/H₂O混合物(水煤气变换反应条件)作为还原剂,可高产率地得到40多种吡咯。除了具有良好的步骤经济性外,这种直接的多米诺过程不需要任何溶剂或外部共催化剂。该方法的一般合成实用性在多种功能化底物上得到了证明,包括生物活性和药学相关化合物的制备,例如(+)-异莫他烷。