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Diazaphospholene-Catalyzed 1,5-HAT of Aryl Halides to Access γ-Spirolactams

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摘要 In the past decades,diazaphospholene hydrides(DAP-H)have emerged as powerful catalysts for a variety of reductive transformations.However,the radical processes with DAPs as catalysts are extremely rare.Herein,a DAP-catalyzed radical process of aryl halides to accessγ-spirolactams through a XAT/1,5-HAT/radical addition/HAT process is presented.This reaction features metal-free conditions and broad functional group tolerance,leading toγ-spirolactams in good yields.
出处 《Chinese Journal of Chemistry》 2025年第18期2313-2317,共5页 中国化学(英文版)
基金 the National Natural Science Foundation of China(No.22201202) the Natural Science Foundation of Zhejiang Province(No.LZ23B020001) Zhejiang Provincial Ten Thousand Talent Program(2023R5244) Open Research Fund of School of Chemistry and Chemical Engineering,Henan Normal University(2020zD04)is gratefully acknowledged.
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