Dehydrogenative α,γ-Diphosphinylation of Allylamines Enabled by Photoinduced Cobaloxime Catalysis.

IF 5 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-11-29 Epub Date: 2024-11-18 DOI:10.1021/acs.orglett.4c03988
Jiefei Guo, Yana Zhang, Miao-Miao Li, Aijun Zhang, Huaixiang Yang, Huan Min, Wei Ding
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Abstract

A regioselective radical α,γ-diphosphinylation of allylamines with secondary phosphine oxides by photoinduced cobaloxime catalysis is described. The reaction tolerates a wide range of allylamines and phosphine oxides, affording α-amino diphosphine dioxides in moderate to good yields with hydrogen evolution. The synthesis of new diphosphine monoxide and diphosphine ligands and the promising antitumor activities of products demonstrate the great potential applications of this approach in catalysis and drug discovery. The detailed mechanism studies indicate that this reaction likely proceeds through a dehydrogenative allylic phosphinylation and nucleophilic addition process.

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光诱导钴肟催化烯丙基胺的α,γ-二膦酰化反应。
介绍了一种通过光诱导钴肟催化烯丙基胺与仲膦氧化物的区域选择性自由基α,γ-二膦化反应。该反应可容忍多种烯丙基胺和膦氧化物,在氢进化的情况下以中等到良好的收率生成α-氨基二磷酸。新的一氧化二膦和二膦配体的合成以及产品良好的抗肿瘤活性证明了这种方法在催化和药物发现方面的巨大应用潜力。详细的机理研究表明,该反应可能是通过脱氢烯丙基膦酰化和亲核加成过程进行的。
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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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