首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis of 4-aryl-5,5-dimethyl-5H-l,2,3-triazoles and 4-aryl-3-cyano-5,5-dimethyl A~1-pyrazolines by cycloaddition of 2-diazopropane with iminoethers and propenenitriles
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Synthesis of 4-aryl-5,5-dimethyl-5H-l,2,3-triazoles and 4-aryl-3-cyano-5,5-dimethyl A~1-pyrazolines by cycloaddition of 2-diazopropane with iminoethers and propenenitriles

机译:2-重氮丙烷与亚氨基醚和丙烯腈的环加成反应合成4-芳基-5,5-二甲基-5H-1,2,3-三唑和4-芳基-3-氰基-5,5-二甲基A〜1-吡唑啉

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摘要

A regiospecific 1,3-dipolar cycloaddition of 2-diazopropane 3 to iminoethers la-c,carried out at 0 deg C,afforded in two steps the corresponding 4-aryl-5,5-dimethyl-5H-l,2,3-triazoles 5a-c.Under the same conditions,3-arylpropenenitriles 2a-d led to 3-cyano-5,5-dimethyl DELTA~1-pyrazoLines 6a-d.Products 4-6 were obtained in good yields (69-85%).
机译:2-重氮丙烷3与亚氨基醚la-c的区域特异性1,3-偶极环加成反应在0摄氏度进行,分两步得到相应的4-芳基-5,5-二甲基-5H-1,2,3-在相同条件下,3-芳基丙烯腈2a-d生成3-氰基-5,5-二甲基DELTA〜1-吡唑啉6a-d。以高收率获得了产品4-6(69-85% )。

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