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Preparation and X-ray structural study of 1-arylbenziodoxolones

机译:1-芳基苯并恶唑酮的制备及X射线结构研究

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摘要

Various 1-arylbenziodoxolones can be conveniently prepared from 2-iodobenzoic acid and arenes by a one-pot procedure using Oxone (2KHSO _5·KHSO_4·K_2SO_4) as an inexpensive and environmentally safe oxidant. This procedure is also applicable for the synthesis of the 7-methylbenziodoxolone ring system using 2-iodo-3-methylbenzoic acid as starting compound. Structures of four 1-arylbenziodoxolone derivatives were established by single-crystal X-ray diffraction analysis. An enhanced reactivity of 1-aryl-7-methylbenziodoxolones toward nucleophiles compared to unsubstituted 1-arylbenziodoxolones has been found.
机译:可以使用一酮(2KHSO _5·KHSO_4·K_2SO_4)作为廉价且对环境安全的氧化剂,通过一锅法从2-碘苯甲酸和芳烃方便地制备各种1-芳基苯并恶恶唑酮。该方法也适用于使用2-碘-3-甲基苯甲酸作为起始化合物的7-甲基苯并恶唑啉酮环系统的合成。通过单晶X射线衍射分析建立了四个1-芳基苯并恶唑酮衍生物的结构。与未取代的1-芳基苯并恶唑啉酮相比,已发现1-芳基-7-甲基苯并恶唑烷酮对亲核试剂的反应性增强。

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