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作 者:Zhang Yan Luo Sha Feng Bainian Zhu Chengjian
机构地区:[1]School of Medicine and Pharmaceutics, Jiangnan University, Wuxi, diangsu 214122, China [2]State Key Laboratry of Coordination Chemistrry, School of Chemistry and Chemical Engi,eering, Nanjing University, Nanjing, Jiangsu 210093, China
出 处:《Chinese Journal of Chemistry》2012年第12期2741-2746,共6页中国化学(英文版)
摘 要:Nitrogen-containing heterocyclic compounds are important motifs of pharmaceuticals and functional materials, and there has been a growing interest in new synthetic methods for their preparations. In this paper, we report a direct cross-coupling reaction of indole with N-aryl tetrahydroisoquinolines in the presence of gold catalyst. The reaction is compatible with a wide range of substituted indoles, to enable the tbrmation of various alkylated heteroarenest, nder very mild reaction conditions.Nitrogen-containing heterocyclic compounds are important motifs of pharmaceuticals and functional materials, and there has been a growing interest in new synthetic methods for their preparations. In this paper, we report a direct cross-coupling reaction of indole with N-aryl tetrahydroisoquinolines in the presence of gold catalyst. The reaction is compatible with a wide range of substituted indoles, to enable the tbrmation of various alkylated heteroarenest, nder very mild reaction conditions.
关 键 词:C-H activation sp3 bonds indolation GOLD heterocyclic compounds
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