首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of 4-aryl-1H-1,2,3-triazoles through TBAF-catalyzed [3+2] cycloaddition of 2-aryl-1-nitroethenes with TMSN3 under solvent-free conditions
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Synthesis of 4-aryl-1H-1,2,3-triazoles through TBAF-catalyzed [3+2] cycloaddition of 2-aryl-1-nitroethenes with TMSN3 under solvent-free conditions

机译:在无溶剂条件下,通过TBAF催化2-芳基-1-硝基乙烯的[3 + 2]环加成反应与TMSN3合成4-芳基-1H-1,2,3-三唑

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摘要

TBAF-catalyzed [3 + 2] cycloaddition reactions of 2-aryl-1-cyano- or 2-aryl-1-carbethoxy-1-nitroethenes 1 with TMSN3 under SFC allow the corresponding 4-aryl-5-eyano- or 4-aryl-5-carbethoxy-1H-1,2,3-triazoles 2 to be prepared under mild reaction conditions and with good to excellent yields (70-90%). The proposed protocol does not require dried glassware or inert atmosphere.
机译:在SFC下,TBAF催化的2-芳基-1-氰基或2-芳基-1-甲乙氧基-1-硝基乙烯1与TMSN3的[3 + 2]环加成反应使相应的4-芳基-5-eyano-或4-在温和的反应条件下制备芳基-5-乙氧基-1H-1,2,3-三唑2,收率好至极好(70-90%)。拟议的协议不需要干燥的玻璃器皿或惰性气氛。

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