Palladium-Catalyzed Decarboxylative Ortho-Ethoxycarbonylation of O‑Methyl Ketoximes and 2‑Arylpyridines with Potassium Oxalate Monoester
journal contributionposted on 02.10.2015, 00:00 authored by Zhong-Yuan Li, Guan-Wu Wang
A novel method for introducing an ester group via palladium-catalyzed ligand-directed C–H activation has been explored. The ortho-ethoxycarbonylation of O-methyl ketoximes proceeded smoothly with the nontoxic and easily handled reagent potassium oxalate monoester, affording the desired products in moderate to good yields. Furthermore, pyridine could also be employed as a directing group to obtain similar results in this transformation.