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Regio- and Stereo-Selective Intermolecular Hydroamidation of Ynamides: An Approach to ( Z)-Ethene-1,2-Diamides.

Zhiyuan PengZhenming ZhangYongliang TuXianzhu ZengJunfeng Zhao
Published in: Organic letters (2018)
An efficient intermolecular trans-selective β-hydroamidation of ynamides to furnish a series of ( Z)-ethene-1,2-diamide derivatives with excellent regio- and stereo-selectivities is described. The trans-β-addition reactions have been illustrated for a wide range of substrates and proceeded under basic reaction conditions using readily available materials in the absence of a transition-metal catalyst. The synthetic approach to these novel ( Z)-ethene-1,2-diamide derivatives paves the way for further exploration of their synthetic application.
Keyphrases
  • transition metal
  • energy transfer
  • structure activity relationship
  • ionic liquid
  • room temperature
  • highly efficient
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  • metal organic framework
  • quantum dots