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Iron-catalyzed hydroaminocarbonylation of alkynes:Selective and efficient synthesis of primaryα,β-unsaturated amides
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作者 Zijun Huang Jia Tang +7 位作者 Xiongwei Jiang Tianle Xie Minmin Zhang Donghui Lan shaofeng pi Zhengde Tan Bing Yi Yuehui Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第11期4842-4845,共4页
α,β-Unsaturated primary amides are important intermediates and building blocks in organic synthesis.Herein,we report a ligand-free iron-catalyzed hydroaminocarbonylation of alkynes using NH_(4)HCO_(3)as the ammonia ... α,β-Unsaturated primary amides are important intermediates and building blocks in organic synthesis.Herein,we report a ligand-free iron-catalyzed hydroaminocarbonylation of alkynes using NH_(4)HCO_(3)as the ammonia source,enabling the highly efficient and regioselective synthesis of linearα,β-unsaturated primary amides.Various aromatic and aliphatic alkynes are transformed into the desired linearα,β-unsaturated primary amides in good to excellent yields.Further studies show that using NH_(4)HCO_(3)as the ammonia source is key to obtain good yields and selectivity.The utility of this route is demonstrated with the synthesis of linearα,β-unsaturated amides including vanilloid receptor-1 antagonist TRPV-1. 展开更多
关键词 Iron-catalyzed ALKYNES Ammonium bicarbonate AMINOCARBONYLATION Linearα β-unsaturated amides
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