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首页> 外文期刊>ACS Omega >K2CO3-Catalyzed Rapid Conversion of N-Sulfonylhydrazones to Sulfinates
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K2CO3-Catalyzed Rapid Conversion of N-Sulfonylhydrazones to Sulfinates

机译:K2CO3催化的N-磺酰腙快速转化为硫酸盐

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摘要

N -Sulfonylhydrazones derived from alkyl, aryl, and heteroaryl aldehydes and ketones undergo rapid conversion into the corresponding sulfinates when heated with 10 mol % K_(2)CO_(3) in N ,N ′-dimethylethylene urea (DMEU) at elevated temperature. The reaction conditions are amenable to several functional groups and suitable for gram-scale synthesis. Under these base-catalyzed conditions, N -tosylhydrazones derived from O -allylated and O -propargylated 2-hydroxyarylaldehydes do not undergo the well-established intramolecular [3 + 2]-cycloaddition reactions and generate corresponding sulfinates in good yields. The base-catalyzed transformation proceeds via crucial rapid intermolecular protonation of the diazo intermediate 11 to generate diazonium ion 12 , which upon nucleophilic displacement by the sulfonyl ion 10 provides the desired sulfinate selectively.
机译:<当用10mol%K_(2)CO_(3)在 N'中加热时,衍生自烷基,芳基和杂芳基醛和酮经历快速转化为相应的硫酸盐的快速转化为相应的硫酸盐。升高温度下二甲基乙烯脲(DMEU)。反应条件适用于几个官能团,适用于革兰氏尺寸合成。在这些碱催化条件下,衍生自源于 11的至关重要的分子分子质原料进行,以产生重氮离子 12,其在通过磺酰离子的亲核位移时,选择性地提供所需的硫酸盐。

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