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One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts

机译:N-杂芳基碘鎓盐的一锅法合成及应用

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摘要

An efficient one-pot synthesis of N-heteroaryl iodonium triflates from the corresponding N-heteroaryl iodide and arene has been developed. The reaction conditions resemble our previous one-pot syntheses, with suitable modifications to allow N-heteroaryl groups. The reaction time is only 30 min, and no anion exchange is required. The obtained iodonium salts were isolated in a protonated form, these salts can either be employed directly in applications or be deprotonated prior to use. The aryl groups were chosen to induce chemoselective transfer of the heteroaryl moiety to various nucleophiles. The reactivity and chemoselectivity of these iodonium salts were demonstrated by selectively introducing a pyridyl moiety onto both oxygen and carbon nucleophiles in good yields.
机译:已经开发了由相应的N-杂芳基碘化物和芳烃有效地一锅合成N-杂芳基碘鎓三氟甲磺酸盐的方法。反应条件类似于我们以前的一锅合成法,并进行了适当的修饰以允许N-杂芳基。反应时间仅为30分钟,并且不需要阴离子交换。分离出的质子化形式的碘鎓盐,这些盐既可以直接用于应用,也可以在使用前去质子化。选择芳基以诱导杂芳基部分向各种亲核试剂的化学选择性转移。这些碘鎓盐的反应性和化学选择性通过以高收率选择性地将吡啶基部分引入氧和碳亲核试剂上来证明。

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