Ru催化电氧化C-H / O-H键偶联:邻苯酞和萘[1,8-bc]呋喃†的制备

IF 4.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Nilam Patil , Ajay Dhapate , Twinkle Bharadwaj , Bhalchandra M. Bhanage
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引用次数: 0

摘要

本文报道了钌催化丙烯酸酯与苯甲酸和萘酚的电氧化偶联,用于合成邻苯酞和萘呋喃衍生物。该工艺对使用钌催化剂激活弱配位O-H键特别有效。这种方法对于碳氢键和氢氧键的活化是可行的,并且组织良好,在超过26种现成的底物上显示出中等到良好的产率。该方法在无氧化剂和无添加剂的条件下进行,显著缩短了反应时间,同时保留了广泛的底物范围。我们的方法提供了一种绿色友好的方法,通过弱配位O-H和C-H键激活,利用电作为氧化剂来合成邻苯酞和萘呋喃。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans†

Electrooxidative C–H/O–H bond coupling via Ru catalysis: access to phthalides and naphtho[1,8-bc]furans†
We hereby report ruthenium-catalyzed electrooxidative coupling of acrylates with benzoic acids and naphthol for the synthesis of phthalide and naphthofuran derivatives. The process is particularly effective for activating weakly coordinating O–H bonds using ruthenium catalysts. This method is workable and well-organized for the activation of carbon–hydrogen and oxygen–hydrogen bonds, demonstrating moderate to good yields across a diverse set of over 26 readily available substrates. The method proceeds under oxidant- and additive-free conditions, significantly reducing the reaction time while retaining a broad substrate scope. Our approach provides a green and user-friendly method for synthesizing phthalides and naphthofurans via weak coordination O–H and C–H bond activation, leveraging electricity as an oxidant.
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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