Center for Chemistry, ICTM institute, University of Belgrade, Njegoševa 12, 11 000 Belgrade, Serbia.
Org Biomol Chem. 2019 Jul 14;17(26):6420-6425. doi: 10.1039/c9ob01090d. Epub 2019 Jun 21.
The organocatalyzed Mannich reaction of unsubstituted and N-aryl-substituted tetrahydroisoquinolines (THIQs) and the Strecker reaction of several N-aryl-substituted THIQs through dehydrogenative C(sp3)-H bond functionalization (cross-dehydrogenative coupling) promoted by organic single electron oxidants DDQ and IBX are presented. The C-H oxidation/Mannich reaction of less reactive N-aryl substituted pyrrolidines is achieved via metal catalyzed photoredox catalysis. Operationally simple procedures provide desired products in an effective and time preserving manner.
本文报道了未取代的和 N-芳基取代的四氢异喹啉(THIQs)的有机催化曼尼希反应,以及通过有机单电子氧化剂 DDQ 和 IBX 促进的脱氢 C(sp3)-H 键官能化(交叉脱氢偶联)的几种 N-芳基取代的 THIQs 的斯特雷克反应。通过金属催化光氧化还原催化,实现了反应活性较低的 N-芳基取代的吡咯烷的 C-H 氧化/Mannich 反应。操作简单的程序以有效和节省时间的方式提供所需的产物。