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A novel and efficient method for the synthesis of β-triazolylalkenes via the phase transfer catalyzed wittig reaction

机译:相转移催化wittig反应合成β-三唑基烯烃的新方法

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N-Alkylation of phosphonium salt 1 with 1H-1,2,4-triazole gave γ-triazolylpropyltriphenylphosphonium bromide 2, which reacted with aromatic aldehydes 3 under the phase transfer conditions ot afford β-triazolylalkenes 4. The synthesis and biological activity of azole compounds have received continuing attention in the last three decades~1. Many N-vinyl azoles were found to be effective fungicides and plant growth regulators, such as diniconazole (S-3308) and uniconazole (S-3307). As part of an ongoing programme and interest in the ylide chemistry and biologically active compounds~2, here we wish to report a novel and efficient method for the synthesis of β-triazolylalkenes via the phase transfer catalyzed Wittig reaction.
机译:1盐1与1H-1,2,4-三唑进行N-烷基化反应,得到γ-三唑基丙基三苯基溴化2,2,在相转移条件下与芳族醛3反应,得到β-三唑基烯烃4。唑化合物的合成及生物活性在过去的三十年里一直受到持续关注。发现许多N-乙烯基唑是有效的杀菌剂和植物生长调节剂,例如diniconazole(S-3308)和uniconazole(S-3307)。作为正在进行的计划的一部分以及对叶立德化学和生物活性化合物的兴趣,我们希望报告一种通过相转移催化的Wittig反应合成β-三唑基烯烃的新颖有效的方法。

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