Key points are not available for this paper at this time.
The selective functionalization of remote C–H bonds in free primary amines holds significant promise for the late-stage diversification of pharmaceuticals. However, to date, the direct functionalization of the meta position of amine substrates lacking additional directing groups remains underexplored. In this Letter, we present a successful meta-C–H arylation of free primary amine derivatives using aryl iodides, resulting in synthetically valuable yields. This meta-selective C–H functionalization is achieved through a sequence involving native amino-directed Pd-catalyzed seven-membered cyclometalation, followed by the utilization of a norbornene-type transient mediator.
Building similarity graph...
Analyzing shared references across papers
Loading...
Shasha Zhang
Gong Zhang
Jie Wang
Zhejiang Wanli University
Organic Letters
Fujian Medical University
Fujian Normal University
Building similarity graph...
Analyzing shared references across papers
Loading...
Zhang et al. (Wed,) studied this question.
synapsesocial.com/papers/68e732cdb6db6435876ac1bd — DOI: https://doi.org/10.1021/acs.orglett.4c00721