茴香醚
催化作用
限制
配体(生物化学)
试剂
化学
芳基
组合化学
基质(水族馆)
分子
反应条件
有机化学
受体
生物化学
机械工程
烷基
海洋学
工程类
地质学
作者
Kezuan Deng,Verena Sukowski,M.A. Fernandez-Ibanez
标识
DOI:10.1002/anie.202400689
摘要
Non-directed C-H arylation is one of the most efficient methods to synthesize biaryl compounds without the need of the prefuctionalization of starting materials, or the installment and removal of directing groups on the substrate. A direct C-H arylation of simple arenes as limiting reactants remains a challenge. Here we disclose a non-directed C-H arylation of anisole derivatives as limiting reagents with aryl iodides under mild reaction conditions. The arylated products are obtained in synthetically useful yields and the arylation of bioactive molecules is also demonstrated. Key to the success of this methodology is the use of a one-step synthesized S,O-ligand.
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