锰催化恶唑啉定向碳氢加成芳烃至不饱和极性键:实验与计算研究。

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Ramiro Robles-Henríquez,Omar Jamis-Oliva,Tomás Chávez-Vega,Susan Lühr,Andrés F Flor-López,Tamara Maldonado,Sebastián Gallardo-Fuentes,Marcelo Vilches-Herrera
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引用次数: 0

摘要

利用锰、钴等丰富的金属在不饱和极性键上直接加成C-H芳烃的方法很少,而且主要局限于以吡啶为导向基团。在这项工作中,我们首次引入了恶唑啉作为这种转化的更通用的基序,它可以在其他官能团中进一步衍生。与大多数报道的mn -四羰基配合物相比,本文提出的机制表明,在催化循环中,碱辅助形成mn -三羰基作为活性物质。实验和DFT研究证实了其机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Manganese-Catalyzed Oxazoline-Directed C-H Addition of Arenes to Unsaturated Polar Bond: Experimental and Computational Study.
The direct C-H aromatic addition to unsaturated polar bonds using abundant metals such as Mn and Co is scarce, and it has been mainly limited to the use of pyridine as a directing group. In this work, we introduce for the first time the use of oxazoline as a more versatile motif for this transformation, which can be further derivatized in other functional groups. The proposed mechanism shows a base-assisted formation of an Mn-tricarbonyl as the active species in the catalytic cycle, in contrast to the most reported Mn-tetracarbonyl complex. The mechanism was validated by experimental and DFT studies.
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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