Hu Long, Dietl Martin C, Han Chunyu, Rudolph Matthias, Rominger Frank, Hashmi A Stephen K
Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im NeuenheimerFeld 270, 69120, Heidelberg, Germany.
Chemistry Department, Faculty of Science, King Abdulaziz University (KAU), 21589, Jeddah, Saudi Arabia.
Angew Chem Int Ed Engl. 2021 May 3;60(19):10637-10642. doi: 10.1002/anie.202016595. Epub 2021 Mar 30.
The development of new methodologies enabling a facile access to valuable heterocyclic frameworks still is an important subject of research. In this context, we describe a dual catalytic cycle merging C-H alkynylation of phenols and oxy-alkynylation of the newly introduced triple bond by using a unique redox property and the carbophilic π acidity of gold. Mechanistic studies support the participation of a bimetallic gold-silver species. The one-pot protocol offers a direct, simple, and regio-specific approach to 3-alkynyl benzofurans from readily available phenols. A broad range of substrates, including heterocycles, is transferred with excellent functional group tolerance. Thus, this methodology can be used for the late-stage incorporation of benzofurans.
开发能够轻松获得有价值的杂环骨架的新方法仍然是一个重要的研究课题。在此背景下,我们描述了一种双催化循环,通过利用金独特的氧化还原性质和亲碳π酸度,将酚的C-H炔基化与新引入的三键的氧-炔基化相结合。机理研究支持双金属金-银物种的参与。该一锅法提供了一种从容易获得的酚直接、简单且区域特异性地合成3-炔基苯并呋喃的方法。包括杂环在内的广泛底物在具有优异官能团耐受性的情况下进行转化。因此,该方法可用于苯并呋喃的后期引入。