铱催化的选择性还原 N-甲酰化和 N-杂环戊烯的转移加氢反应

IF 2.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Renshi Luo, Sen Wang, Yuqiu Liang, Jinghui Tong, Jianhua Liao and Lu Ouyang*, 
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引用次数: 0

摘要

选择性官能化在生物活性化合物和药物的改性方面有许多潜在的应用。在此,我们以 IrIII 复合物为催化剂,提出了一种选择性还原 N-甲酰化 N-庚烯和转移氢化的新方法。溶剂、甲酸(FA)当量、反应温度和铱催化剂的组合具有很高的产物选择性,能以极好的收率生成不同选择性的还原 N-甲酰化和转移氢化产物。在此过程中,在不同的反应条件下,甲酸不仅可以用作氢源,还可以用作还原性 N-甲酰化试剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ir-Catalyzed Selective Reductive N-Formylation and Transfer Hydrogenation of N-Heteroarenes

Ir-Catalyzed Selective Reductive N-Formylation and Transfer Hydrogenation of N-Heteroarenes

Selective functionalization has numerous potential applications in the modification of bioactive compounds and pharmaceuticals. Herein, we advance a new approach for the selective reductive N-formylation of N-heteroarenes and transfer hydrogenation using IrIII complexes as catalysts. The combination of solvent, equivalent of formic acid (FA), reaction temperature, and iridium catalyst exerts high product selectivity, delivering divergent selective formations of reductive N-formylation and transfer hydrogenation products in excellent yields. In this process, FA can be employed as not only the hydrogen source but also the reductive N-formylation reagent under different reaction conditions.

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来源期刊
Organometallics
Organometallics 化学-无机化学与核化学
CiteScore
5.60
自引率
7.10%
发文量
382
审稿时长
1.7 months
期刊介绍: Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.
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