在N,N-配体和无氢化物条件下,钴催化丙炔醇还原合成1,3-二芳烯。

IF 3.7 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Luyao Wei, Biao Zhu, Luning Tang, Zhengyu Han, Jianwei Sun, Hai Huang
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引用次数: 0

摘要

烯类化合物是一类重要的有机化合物,其合成一直是人们关注的热点。在这篇文章中,我们开发了一种钴催化光氧化还原策略,为丙炔醇合成1,3-二芳烯提供了一种替代和有效的方法。该反应利用有机胺作为氢源,避免了常规氢化物添加剂的使用,并且不需要额外添加配体来激活钴催化剂,达到了温和的反应条件。结果表明,该反应能够合成所需的1,3-二芳烯化合物,且产率和官能团相容性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions

Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions

Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions

Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions

Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions

Allenes are a class of important organic compounds, and their synthesis has always been of great interest. In this article, we have developed a cobalt-catalyzed photoredox strategy, providing an alternative and efficient approach for the synthesis of 1,3-diarylallenes from propargyl alcohols. The reaction utilized organic amines as a hydrogen source to avoid the use of conventional hydride additives and does not require the addition of extra N,N-ligands to activate the cobalt catalyst, achieving a mild reaction condition. As a result, the reaction was able to synthesize the desired 1,3-diarylallene compounds with good yields and functional group compatibility.

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来源期刊
Chemistry - A European Journal
Chemistry - A European Journal 化学-化学综合
CiteScore
7.90
自引率
4.70%
发文量
1808
审稿时长
1.8 months
期刊介绍: Chemistry—A European Journal is a truly international journal with top quality contributions (2018 ISI Impact Factor: 5.16). It publishes a wide range of outstanding Reviews, Minireviews, Concepts, Full Papers, and Communications from all areas of chemistry and related fields. Based in Europe Chemistry—A European Journal provides an excellent platform for increasing the visibility of European chemistry as well as for featuring the best research from authors from around the world. All manuscripts are peer-reviewed, and electronic processing ensures accurate reproduction of text and data, plus short publication times. The Concepts section provides nonspecialist readers with a useful conceptual guide to unfamiliar areas and experts with new angles on familiar problems. Chemistry—A European Journal is published on behalf of ChemPubSoc Europe, a group of 16 national chemical societies from within Europe, and supported by the Asian Chemical Editorial Societies. The ChemPubSoc Europe family comprises: Angewandte Chemie, Chemistry—A European Journal, European Journal of Organic Chemistry, European Journal of Inorganic Chemistry, ChemPhysChem, ChemBioChem, ChemMedChem, ChemCatChem, ChemSusChem, ChemPlusChem, ChemElectroChem, and ChemistryOpen.
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