Chem. J. Chinese Universities ›› 2003, Vol. 24 ›› Issue (9): 1592.

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Studies on Synthesis of 2-Substituted-purine Derivatives

LIU Fu-Sheng1, YU Shi-Tao1, GE Xiao-Ping1, YANG Jin-Zong2   

  1. 1. College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China;
    2. State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012, China
  • Received:2002-09-23 Online:2003-09-24 Published:2003-09-24

Abstract: The Stille coupling reaction between 2-iodo-9-benzylpurine and RSnBu3and the nucleophilic addition and cycloaddition of 2-vinyl-9-benzylpurine were studied. Aseries of new 2-substituted purined-erivatives were synthesized and characterized by elemental analysis, 1HNMR, 13CNMR and MS. It was demonstrated that the reaction mechanism between 2-vinyl-9-benzylpurine and benzenethiol was oxidative addition rather than nucleophilic addition. The structure of the main product was determined by single-crystal X-ray method.

Key words: 2-Iodo-purine, 2-Vinyl-purine, Stille coupling, Nucleophilic addition, Cycloaddition

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