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Palladium-Catalyzed Imidoylation-Triggered [2 + 2 + 1] Cyclization of Internal Alkyne with Isocyanides.

Keke HuangJin-Biao LiuZhi-Feng ChenYu-Chao WangSarita YadavGuanyinsheng Qiu
Published in: Organic letters (2020)
In this work, a palladium-catalyzed [2 + 2 + 1] cyclization of internal alkynes with double isocyanides is described. This facile procedure is efficient for synthesizing various pyrrolo[3,2-c]quinolin-2-amines. The reaction worked well with a broad reaction scope. In the process, it is believed that sequential double isocyanide insertion, 6-exo-dig cyclization of alkyne, and addition of an imino group are involved.
Keyphrases
  • minimally invasive
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  • electron transfer