钯/银/配体协同催化 2,1,3-苯并二唑的 C-H 烯化反应

IF 4.4 2区 化学 Q2 CHEMISTRY, APPLIED
Siyeon Jeong, Chaerin Lee, Jung Min Joo
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引用次数: 0

摘要

钯和银络合物的组合已成为 C-H 活化的双金属催化体系,其性能经常优于纯钯体系。除了银 (I) 盐作为氧化剂、卤化物清除剂和路易斯酸的传统作用外,钯银双金属协同作用已被证明可促进 C-H 裂解。在本研究中,我们探讨了在钯银双金属催化体系中加入吡唑吡啶酮(PzPyOH)配体,从而共同促进 C-H 裂解和迁移插入过程。这种协同方法使 2,1,3-苯并噻二唑、2,1,3-苯并噁二唑和 2,1,3-苯并三唑在 C4 位与烯烃发生脱氢 C-H 烯化反应。这些结果表明,将新型配体与杂多金属系统结合起来,可以促进 C-H 裂解以外的其他基本步骤,这表明它们在 C-H 功能化方面具有更广泛的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synergistic Palladium/Silver/Ligand Catalysis for C−H Alkenylation of 2,1,3-Benzofused Heterodiazoles

Synergistic Palladium/Silver/Ligand Catalysis for C−H Alkenylation of 2,1,3-Benzofused Heterodiazoles

The combination of palladium and silver complexes has emerged as a bimetallic catalytic system in C−H activation, frequently outperforming palladium-only systems. Beyond the conventional roles of silver (I) salts serving as oxidants, halide scavengers, and Lewis acids, Pd−Ag bimetallic synergism has been shown to facilitate C−H cleavage. In this study, we explore the incorporation of a pyrazolopyridone (PzPyOH) ligand into a Pd−Ag bimetallic catalytic system, which together promote both C−H cleavage and migratory insertion processes. This synergistic approach enables dehydrogenative C−H alkenylations at the C4 position of 2,1,3-benzothiadiazole, 2,1,3-benzoxadiazole, and 2,1,3-benzotriazole with alkenes. These results demonstrate the potential of combining novel ligands with heterobimetallic systems to facilitate other elementary steps beyond C−H cleavage, suggesting their broader applicability in C−H functionalization.

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来源期刊
Advanced Synthesis & Catalysis
Advanced Synthesis & Catalysis 化学-应用化学
CiteScore
9.40
自引率
7.40%
发文量
447
审稿时长
1.8 months
期刊介绍: Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry. The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.
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