碘化阴离子可实现还原性交叉亲电偶联,从而制备叔胺。

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Miran Lemmerer, Veronica Tona, David Just, Miloš Vavrík, Boris Maryasin, Giovanni Di Mauro, Andreas B Zur Bonsen, Daniel Kaiser, Nuno Maulide
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引用次数: 0

摘要

碘阴离子的还原能力是一种尚未被充分开发的特性,可用于有机分子的交叉亲电偶联。在本文中,我们利用这一特性,通过两种简单试剂的组合制备叔胺:亲电碳前体和碘化亚胺的双重作用--既是含氮结构单元,又是还原剂。通过实验和量子化学计算的结合,探索了这种新的 C-C 键形成模式的基本机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Iodide anion enables a reductive cross-electrophile coupling for preparing tertiary amines.

The reducing power of iodide anion is an underexplored property that can be used for the cross-electrophile coupling of organic molecules. Herein we harness this trait for the preparation of tertiary amines through the combination of two simple reagents: an electrophilic-carbon precursor and an iminium iodide in a dual role-both as nitrogen-containing building block and as reducing agent. The underlying mechanism of this new C-C bond-formation paradigm is explored through a combination of experiment and quantum chemical calculations.

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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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