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通过光诱导烯烃还原二膦化构建双齿膦

Construction of Bidentate Phosphines Enabled by Photoinduced Reductive Diphosphination of Alkenes.

作者信息

Liu Hongchi, Huang Hanmin

机构信息

Key Laboratory of Precision and Intelligent Chemistry, Department of Chemistry, University of Science and Technology of China, Hefei, 230026, P. R. China.

Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education, Huaibei Normal University, Huaibei, 235000, P. R. China.

出版信息

Chemistry. 2024 Apr 11;30(21):e202304109. doi: 10.1002/chem.202304109. Epub 2024 Feb 26.

Abstract

The diphosphination of alkenes through a radical pathway offers a promising approach for the rapid construction of aryl bisphosphines. However, such a synthetic strategy has not been successfully applied to the preparation of alkyl bisphosphines, partially due to the difficulties in the generation of phosphorus-centered radicals from common alkyl phosphine compounds. We herein demonstrate that this challenge can be overcome by hiring Janus-faced chlorophosphine as the phosphine source that can act as not only a radical precursor to generate phosphine-centered radicals but also a radicalphile to capture alkyl radicals. With this novel strategy, a photocatalyzed reductive diphosphination reaction has been established, allowing for a straightforward synthesis of both aryl and alkyl 1,2-bisphosphines from readily accessible alkenes and chlorophosphines.

摘要

通过自由基途径实现烯烃的二膦化反应为快速构建芳基双膦提供了一种有前景的方法。然而,这种合成策略尚未成功应用于烷基双膦的制备,部分原因是从常见的烷基膦化合物生成以磷为中心的自由基存在困难。我们在此证明,通过使用具有两面性的氯膦作为膦源可以克服这一挑战,该氯膦不仅可以作为产生以膦为中心的自由基的自由基前体,还可以作为捕获烷基自由基的亲自由基试剂。基于这种新策略,已建立了光催化还原二膦化反应,可从易于获得的烯烃和氯膦直接合成芳基和烷基1,2 - 双膦。

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