1,n-Enynes 与以磷为中心的自由基发生自由基反应的最新进展

IF 1.9 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY ChemistrySelect Pub Date : 2024-11-07 DOI:10.1002/slct.202404010
Hairui Ni, Siyan Fan, Tongyan Yu, Zhuang-zhi Shi, Dr. Siliang You, Dr. Chao Deng
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摘要

由于具有广泛的生物活性,有机磷化合物已作为非手性和手性配体广泛应用于有机合成(PPh3、BINAP、dppe、Duphos、Xantphos、PPFA、Chiraphos、SEGPHOS)、阻燃剂、功能材料(LED、PV)以及农用化学品和医药领域。1,n-烯炔烃是一种用途广泛的特殊结构单元,基于其两个活性不饱和化学键(C═C 双键和 C≡C 三键),已成功应用于合成各种功能化环状化合物。随着高选择性和高效有机化学方法的发展,近年来通过自由基级联策略合成各种有机磷环状化合物引起了广泛关注。在此,我们总结了近年来 1,n-烯炔与以磷为中心的自由基级联反应的主要成果。此外,我们还在这篇综述中展示了详细的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Recent Advances in Radical Reactions of 1,n-Enynes with Phosphorus-Centered Radicals

Organophosphorus compounds have been widely used as achiral and chiral ligands in organic synthesis (PPh3, BINAP, dppe, Duphos, Xantphos, PPFA, Chiraphos, SEGPHOS), flame retardants, functional materials (LED, PV), as well as agrochemicals and medicines due to their broad biological activities. As the privileged versatile building blocks, 1,n-enynes have been successfully applied in the synthesis of various functionalized cyclic compounds based on their two active unsaturated chemical bonds (C═C double and C≡C triple bonds). With the development of highly selective and efficient methods in organic chemistry, various organophosphorus cyclic compounds synthesis through radical cascade strategy has attracted considerable attention in recent years. In here, we have summarized the recent main achievements in the radical cascade reactions of 1,n-enynes with phosphorus-centered radicals. Furthermore, we also displayed the detailed reaction mechanisms in this review.

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来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
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