化学
烷基
基质(水族馆)
还原消去
表面改性
催化作用
组合化学
功能群
反应中间体
药物化学
联轴节(管道)
反应条件
偶联反应
有机化学
卤化
群(周期表)
氧化还原
反应机理
作者
Jinping Yuan,Shuang Tang,Yu Pu,Xianrong Chen,Yi Yang,Feng Zhang
标识
DOI:10.1021/acs.orglett.6c04082
摘要
Abstract The coupling reaction of highly reactive heteroaryl iodides and alkyl iodides remains a longstanding challenge because of competing side reactions, including dehalogenation, hydrogenation, homocoupling, and radical dimerization. Here, we report an iron-catalyzed reductive cross-coupling of heteroaryl iodides with alkyl iodides enabled by a hydrosilane-based reducing system. This strategy provides efficient access to C(sp2)–C(sp3) bonds and exhibits a broad substrate scope, good functional group tolerance, gram-scale scalability, and applicability to the late-stage functionalization of complex bioactive molecules. Mechanistic studies support the involvement of alkyl radical intermediates and low-valent iron species, with an iron(0) complex proposed as a catalytically relevant intermediate.
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