Oxidative Phosphorylation of Silyl Enol Ethers with H-Phosphine Oxides via Dual Cobaloxime and Photoredox Catalysis

IF 4.7 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2026-10-19 DOI:10.1021/acs.orglett.6c03987
Yong-Hao Ma,Wei Shi,Jing Wu,Xuefei Zhao,Teck-Peng Loh,Xu-Hong Hu
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Abstract

We report herein a visible-light-induced dual catalytic system merging cobaloxime and photoredox catalysis that enables the oxidative phosphorylation of silyl enol ethers with H-phosphine oxides. This method provides efficient access to diverse β-ketophosphine oxides, bypassing the need for external oxidants, harsh conditions, or a restricted substrate scope that typically plagues conventional methods. Salient features include easily accessible starting materials, broad functional group compatibility, late-stage modifications, and scalability. Mechanistic studies reveal that this formal oxidative phosphorylation of ketones proceeds via a phosphinoyl radical intermediate.

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双钴肟光氧化还原催化下硅烯醚与h -膦氧化物的氧化磷酸化
我们在此报道了一个可见光诱导的双催化系统,它融合了钴胺肟和光氧化还原催化,使硅烯醇醚与h -膦氧化物的氧化磷酸化成为可能。该方法提供了对各种β-酮膦氧化物的有效获取,绕过了通常困扰传统方法的外部氧化剂、恶劣条件或受限制的底物范围的需要。突出的特性包括易于访问的起始材料、广泛的官能团兼容性、后期修改和可伸缩性。机制研究表明,酮的这种正式氧化磷酸化是通过一个磷酸酰基自由基中间体进行的。
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来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
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