Photoelectrocatalyzed Alkylation of Phosphonites by Direct Decarboxylative C(sp3)-P Coupling

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2025-01-26 DOI:10.1002/anie.202500744
Kang-Ning Yuan, Tian Xie, Jia-Bao Wang, Prof. Dr. Dali Wang, Prof. Dr. Ming Shang
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Abstract

A photoelectrocatalytic method is presented that achieves direct decarboxylative C(sp3)-P coupling, providing a modular route to alkylphosphinates and alkylphosphonates from readily available carboxylic acids. The success of this reaction hinges on the synergistic combination of electrochemical anodic oxidation and photocatalytic ligand to metal charge transfer (LMCT) decarboxylation. By employing P(III) reagents as limiting reagents, our approach enables efficient alkyl modification of medicinally important nucleosides and complex molecules derived phosphonites, which were challenging to access by existing methods. Detailed mechanistic studies elucidate the critical roles of Fe catalysts and additives, offering valuable insights into the reaction pathway and laying the foundation for future advancements in photoelectrocatalytic C(sp3)-heteroatom bond-forming reactions.

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直接脱羧C(sp3) - P偶联的光电催化膦酸盐烷基化反应
提出了一种实现直接脱羧C(sp3) -P偶联的光电催化方法,为从现成的羧酸中制备烷基膦酸盐和烷基膦酸盐提供了模块化途径。该反应的成功取决于电化学阳极氧化和光催化配体对金属电荷转移(LMCT)脱羧的协同结合。通过使用P(III)试剂作为限制试剂,我们的方法能够对药用重要核苷和复杂分子衍生的膦酸盐进行有效的烷基修饰,这是现有方法难以获得的。详细的机制研究阐明了Fe催化剂和添加剂的关键作用,为反应途径提供了有价值的见解,并为光电催化C(sp3) -杂原子成键反应的未来发展奠定了基础。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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