探索可见光通过镍催化形成碳-氮和碳-氧键

Shengqing Zhu , Huan Li , Yingying Li , Zhonghou Huang , Lingling Chu
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引用次数: 1

摘要

含杂原子的基序是药物、农用化学品和功能材料最有优势的支架之一。过渡金属催化的碳-杂原子键形成反应已成为快速组装这些有价值骨架的不可或缺的合成工具。尽管取得了令人印象深刻的进展,但开发在温和条件下用富含地球的催化剂催化构建碳-杂原子键的通用有效方法仍然是非常可取的。利用光激发揭示的新的独特反应性,最近,在可见光驱动的镍催化的碳-杂原子键形成反应领域取得了令人兴奋的进展,使人们能够在异常温和的条件下容易地获得不同的碳-异原子键。在这篇综述中,我们强调了最近通过可见光驱动的高价镍络合物或光激发的镍络合物形成C–N和C–O键的合成方法的发展,并对反应设计和机理场景进行了深入讨论。
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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Exploring visible light for carbon–nitrogen and carbon–oxygen bond formation via nickel catalysis

Heteroatom-containing motifs are one of the most privileged scaffolds for pharmaceuticals, agrochemicals, and functional materials. Transition-metal-catalyzed carbon–heteroatom bond-forming reactions have emerged as an indispensable synthetic tool for the rapid assembly of these valuable skeletons. Despite impressive progress, the development of general and efficient methods for the catalytic construction of carbon–heteroatom bonds with Earth-abundant catalysts under mild conditions is still highly desirable. Utilizing the new and unique reactivity uncovered by photoexcitation, recently, exciting progress has been made in the area of visible-light-driven nickel-catalyzed carbon–heteroatom bond-forming reactions, enabling facile access to diverse carbon–heteroatom bonds under exceptionally mild conditions. In this review, we highlight the recent synthetic methodology development for the formation of C–N and C–O bonds via visible-light-driven high-valent nickel complexes or photoexcited nickel complexes, with in-depth discussions with reaction designs and mechanistic scenarios.

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