Department of Chemistry, Rutgers University , 73 Warren Street, Newark, New Jersey 07102, United States.
J Org Chem. 2016 Dec 2;81(23):12023-12030. doi: 10.1021/acs.joc.6b02294. Epub 2016 Nov 17.
Palladium-catalyzed decarbonylative Heck reaction of amides by chemoselective N-C activation using N-acylsaccharins as coupling partners has been accomplished. These studies represent only the second example of amide-Heck reactions reported to date. A broad range of electronically diverse amide and olefin coupling partners is amenable to this transformation. Orthogonal site-selective Heck cross-couplings by C-Br/N-C cleavage and mechanistic studies are reported. This report introduces readily available, bench-stable, cheap, and benign N-acylsaccharins as aryl transfer reagents to access versatile aryl-metal intermediates.
钯催化酰胺的脱羰基 Heck 反应通过 N-酰基氨基糖作为偶联试剂的化学选择性 N-C 活化来实现。这些研究代表了迄今为止报道的酰胺-Heck 反应的第二个实例。广泛的电子多样性酰胺和烯烃偶联试剂适用于这种转化。通过 C-Br/N-C 断裂进行正交的位点选择性 Heck 交叉偶联以及机理研究也有报道。本报告介绍了易得、稳定、廉价且无害的 N-酰基氨基糖作为芳基转移试剂,以获得多功能芳基金属中间体。