Nickel-catalyzed enantioselective reductive amination of benzylic ketones in alcohols

IF 10.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Science China Chemistry Pub Date : 2024-06-27 DOI:10.1007/s11426-024-2019-1
Xiuhua Wang, Jianrong Steve Zhou
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Abstract

Asymmetric reductive amination directly converts ketones and amines to alkylamines, which are important motifs in medicines. We report that cationic nickel complexes of chiral diphosphines promote enantioselective reductive amination of benzylic ketones with both arylamines and benzhydrazide. Isopropanol was used as a safe and cheap source of hydrogen instead of formic acid. The reaction can be readily applied to a concise synthesis of diarylethylamines, a class of neuroactive substances.

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镍催化的苄基酮在醇中的对映选择性还原胺化反应
不对称还原胺化反应可直接将酮和胺转化为烷基胺,而烷基胺是药物中的重要基团。我们报告了手性二膦的阳离子镍配合物促进了苄基酮与芳基胺和苯肼的对映选择性还原胺化反应。使用异丙醇代替甲酸作为安全廉价的氢源。该反应很容易应用于二芳基乙胺(一类神经活性物质)的简易合成。
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来源期刊
Science China Chemistry
Science China Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
7.30%
发文量
3787
审稿时长
2.2 months
期刊介绍: Science China Chemistry, co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China and published by Science China Press, publishes high-quality original research in both basic and applied chemistry. Indexed by Science Citation Index, it is a premier academic journal in the field. Categories of articles include: Highlights. Brief summaries and scholarly comments on recent research achievements in any field of chemistry. Perspectives. Concise reports on thelatest chemistry trends of interest to scientists worldwide, including discussions of research breakthroughs and interpretations of important science and funding policies. Reviews. In-depth summaries of representative results and achievements of the past 5–10 years in selected topics based on or closely related to the research expertise of the authors, providing a thorough assessment of the significance, current status, and future research directions of the field.
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