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首页> 外文期刊>Beilstein journal of organic chemistry. >Diels–Alder cycloadditions of N-arylpyrroles via aryne intermediates using diaryliodonium salts
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Diels–Alder cycloadditions of N-arylpyrroles via aryne intermediates using diaryliodonium salts

机译:使用二芳基碘鎓盐通过芳烃中间体进行的Diels–Alder环加成N-芳基吡咯

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With a strategy of the formation of benzynes by using diaryliodonium salts, a cycloaddition reaction of N-arylpyrroles with benzynes was reported. A wide range of bridge-ring amines with various substituents have been synthesized in moderate to excellent yields (35–96%). Furthermore, with a catalytic amount of TsOH·H2O, these amines can be converted into the corresponding N-phenylamine derivatives easily, which are potentially useful in photosensitive dyes.
机译:通过使用二芳基碘鎓盐形成苯炔的策略,报道了N-芳基吡咯与苯炔的环加成反应。合成了多种具有各种取代基的桥环胺,产率中等至优异(35-96%)。此外,在催化量的TsOH·H2O的作用下,这些胺可以轻松地转化为相应的N-苯胺衍生物,这可能在光敏染料中有用。

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