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温和条件下有机氧化剂介导的四氢异喹啉的脱氢 C(sp)-H 键官能化。

Dehydrogenative C(sp)-H bond functionalization of tetrahydroisoquinolines mediated by organic oxidants under mild conditions.

机构信息

Center for Chemistry, ICTM institute, University of Belgrade, Njegoševa 12, 11 000 Belgrade, Serbia.

出版信息

Org Biomol Chem. 2019 Jul 14;17(26):6420-6425. doi: 10.1039/c9ob01090d. Epub 2019 Jun 21.

Abstract

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.

摘要

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。

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