Synthesis of Thioethers via Nickel-Catalyzed Cross-Coupling of Aryl Halides with Ketene Dithioacetal

IF 5 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2025-02-09 DOI:10.1021/acs.orglett.4c04692
Baolong Xu, Shaowen Ling, Shuaichen Zheng, Xinyi Feng, Hui Liu, Yunhui Dong, Xinjin Li, Biqiong Hong, Feng-Gang Sun
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Abstract

Herein, we present a nickel-catalyzed C–S cross-coupling between aryl halides and ketene dithioacetals under “base-free” conditions without an exogenous ligand. By employing easily available ketene dithioacetals as sulfide donors, this reaction affords a broad range of unsymmetrical alkyl-aryl sulfides without using odorous and toxic thiols. The newly developed catalytic methodology features an excellent functional group tolerance, wide substrate scope, and diverse downstream synthesis. Preliminary mechanism investigations reveal that a Ni(I)/Ni(III) catalytic cycle might be involved.

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镍催化芳基卤化物与烯基二硫缩醛交偶联合成硫醚
在此,我们提出了在“无碱”条件下,在没有外源配体的情况下,镍催化芳基卤化物和烯酮二硫缩醛之间的C-S交叉偶联。通过使用容易获得的烯酮二硫缩醛作为硫化物供体,该反应提供了广泛的不对称烷基芳基硫化物,而不使用气味和有毒的硫醇。新开发的催化方法具有良好的官能团耐受性,广泛的底物范围和多样化的下游合成。初步机理研究表明,这可能涉及Ni(I)/Ni(III)催化循环。
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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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