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铑催化的卡宾转移反应实现的C-H甲基化和烷基化反应

Rhodium-Catalyzed C-H Methylation and Alkylation Reactions by Carbene-Transfer Reactions.

作者信息

Empel Claire, Jana Sripati, Langletz Tim, Koenigs Rene M

机构信息

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074, Aachen, Germany.

出版信息

Chemistry. 2022 Feb 24;28(12):e202104321. doi: 10.1002/chem.202104321. Epub 2022 Feb 2.

Abstract

In this combined computational and experimental study, the C-H functionalization of 2-phenyl pyridine with diazoalkanes was investigated. Initial evaluation by computational methods allowed the evaluation of different metal catalysts and diazoalkanes and their compatibility in this C-H functionalization reaction. With these findings, suitable reaction conditions for the C-H methylation reactions were quickly identified by using highly reactive TMS diazomethane and C-H alkylation reactions with donor/acceptor diazoalkanes, which is applied to a broad scope on alkylation reactions of 2-aryl pyridines with TMS diazomethane and donor/acceptor diazoalkane (51 examples, up to 98 % yield).

摘要

在这项计算与实验相结合的研究中,对2-苯基吡啶与重氮烷烃的C-H官能化反应进行了研究。通过计算方法进行的初步评估能够对不同的金属催化剂和重氮烷烃及其在该C-H官能化反应中的兼容性进行评估。基于这些发现,通过使用高反应活性的三甲基硅基重氮甲烷以及与供体/受体重氮烷烃的C-H烷基化反应,迅速确定了C-H甲基化反应的合适反应条件,该反应条件广泛应用于2-芳基吡啶与三甲基硅基重氮甲烷以及供体/受体重氮烷烃的烷基化反应(51个实例,产率高达98%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b25/9302633/52493c6bc89d/CHEM-28-0-g004.jpg

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