Front Cover: Development of Organoautocatalyzed Double s-Bond C(sp2)-N Transamination Metathesis Reaction (Angew. Chem. 28/2025)

Volker Klein, Florian Schuster, Jonas Amthor, Harald Maid, Prabhakar Bijalwan, Fahmi Himo, Stefano Santoro, Svetlana B. Tsogoeva
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引用次数: 0

Abstract

Organoautocatalyzed transamination metathesis of challenging cyclic tertiary amines is reported. In their Research Article (e202505275), Svetlana B. Tsogoeva and co-workers demonstrate the use of an in situ-formed pyrrolidinium salt as an efficient organoautocatalyst, enabling double C(sp2)-N bond metathesis at room temperature via a domino reaction mechanism. This metal- and additive-free transformation advances green, waste-reducing, and sustainable approaches in organic synthesis.

Abstract Image

封面:有机自催化双s键C(sp2)-N转氨化反应的研究进展。化学28/2025)
报道了具有挑战性的环叔胺的有机自催化转氨化。在他们的研究文章(e2012505275)中,Svetlana B. Tsogoeva及其同事展示了使用原位形成的吡咯烷盐作为有效的有机自催化剂,通过多米诺反应机制在室温下实现双C(sp2)-N键的转化。这种不含金属和添加剂的转变推进了绿色、减少废物和可持续的有机合成方法。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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