Leibniz-Institut für Katalyse e.V., Albert-Einstein-Str. 29a, 18059 Rostock (Germany).
Angew Chem Int Ed Engl. 2016 Jan 4;55(1):387-91. doi: 10.1002/anie.201508575. Epub 2015 Nov 11.
Reported herein, for the first time, is the selective ruthenium-catalyzed reductive alkoxylation and amination of phthalimides/succinimides. Notably, this novel methodology avoids hydrogenation of the aromatic ring and allows methoxylation of substituted imides with good to excellent selectivity for one of the carbonyl groups. The reported method opens the door to the development of new processes for the selective synthesis of various functionalized N-heterocyclic compounds. As an example, intramolecular reductive couplings to afford tricyclic compounds are presented for the first time.
本文首次报道了邻苯二甲酰亚胺/琥珀酰亚胺的选择性钌催化还原烷氧基化和氨化反应。值得注意的是,这种新方法避免了芳环的氢化,并允许取代的亚胺进行甲氧基化,对其中一个羰基具有良好到优异的选择性。所报道的方法为开发各种功能化的 N-杂环化合物的选择性合成新工艺开辟了道路。例如,首次提出了通过分子内还原偶联来制备三环化合物的方法。