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首页> 外文期刊>Advanced synthesis & catalysis >Palladium-Catalyzed Regioselective Synthesis of 1,2-Fused Indole-Diazepines via [5+2] Annulation of o-Indoloanilines with Alkynes
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Palladium-Catalyzed Regioselective Synthesis of 1,2-Fused Indole-Diazepines via [5+2] Annulation of o-Indoloanilines with Alkynes

机译:钯 - 催化的1,2稠合吲哚-二氮杂豚的区域选择性合成O-吲哚菁的奥基吲哚环素与炔烃

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摘要

An efficient and regioselective palladium(II)-catalyzed [5+2] annulation of unprotected o-indoloanilines with internal alkynes under microwave irradiation has been explored. The diverse imine-containing 1,2-fused indole[1,7-a]diazepines are constructed in moderate to excellent yields. The mechanistic pathway shows pivalic acid and molecular oxygen to play crucial roles for the regeneration of highly active electrophilic palladium species in the catalytic cycle.
机译:探讨了高效且区域选择性钯(II) - 催化[5 + 2]在微波辐射下具有内部炔烃的未受保护的O-吲哚菁的环节。 含有多样的含亚胺1,2稠合的吲哚[1,7-A]直脂胺以中等至优异的产率构建。 机械途径显示靶酸和分子氧,起到在催化循环中的高活性亲电子钯物种的再生的关键作用。

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