可见光驱动的阴离子中继化学(ARC):全取代吡唑的构建

Guodan Lu , Tao Zhang , Xionglve Cheng , Kehan Qian , Yong Wang , Xiaobing Wan
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引用次数: 0

摘要

阴离子接力化学(ARC)是一种多组分结合策略,已成为合成复杂结构的一种强有力的方法。然而,以往的研究主要集中在热控制的反应模式上。在这项研究中,我们报告了一种前所未有的可见光驱动阴离子接力化学(ARC)策略的发展。利用能量转移过程,我们成功地将甲酰腙转化为阴离子给体,促进了在温和条件下合成完全取代的吡唑衍生物。此外,实验机制研究和计算研究(DFT)的结合不仅证实了所提出的反应机制,而且为未来的研究提供了更多的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Visible-light-driven anion relay chemistry (ARC): construction of fully substituted pyrazoles†

Visible-light-driven anion relay chemistry (ARC): construction of fully substituted pyrazoles†
Anion relay chemistry (ARC) is a multi-component union strategy that has emerged as a powerful approach for synthesizing complex structures. However, previous studies have primarily concentrated on thermally controlled reaction modes. In this study, we report the development of an unprecedented visible-light-driven anion relay chemistry (ARC) strategy. Utilizing an energy-transfer process, we successfully transformed tosylhydrazones into anionic donors, facilitating the synthesis of fully substituted pyrazole derivatives under mild conditions. Furthermore, a combination of experimental mechanistic investigations and computational studies (DFT) not only corroborated the proposed mechanism of the reaction but also inspired additional avenues for future research.
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7.80
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