过渡金属催化的炔烃正/反二官能化新趋势

IF 19.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Chem Pub Date : 2024-09-12 DOI:10.1016/j.chempr.2024.07.003
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引用次数: 0

摘要

通过烷的区域选择性邻接双官能化反应直接获得多官能化化合物是一项极具挑战性的合成任务,多年来一直激励着科学界。1997 年发现的 Catellani 反应--一种钯催化的邻位双官能化反应--真正改变了游戏规则。这一新范例为获得正/反双官能化的烯烃提供了多种可能性,多年来备受关注。在这一开创性工作的基础上,创新战略应运而生。本视角概述了催化沧醛炔双官能化领域的最新进展。它强调了当前面临的挑战,并讨论了未来的前景和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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New trends for transition metal-catalyzed ortho/ipso difunctionalizations of arenes

Direct access to polyfunctionalized compounds by regioselective vicinal difunctionalizations of arenes is a challenging synthetic task that inspired the scientific community for years. The discovery of the Catellani reaction in 1997, a palladium-catalyzed vicinal difunctionalization reaction, was a real game-changer. This new paradigm offered various possibilities to access ortho/ipso-difunctionalized arenes and garnered attention over the years. From this pioneering work, innovative strategies have emerged. This perspective provides an overview of recent advances made in the field of catalytic vicinal arene difunctionalizations. It highlights current challenges and discusses future perspectives and opportunities.

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来源期刊
Chem
Chem Environmental Science-Environmental Chemistry
CiteScore
32.40
自引率
1.30%
发文量
281
期刊介绍: Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.
期刊最新文献
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