Diels–Alder Chemistry of Ketenimines: Toward Highly Reactive Aza-Dienophiles

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Authors: Marshall J. Liss, Christopher G. Newton
Cited by: 1
References: 95

Abstract

Abstract The development of new cycloaddition partners remains central to advancing our understanding of molecular structure and pericyclic reactivity, while also enabling increasingly convergent synthetic strategies. In this context, the development of heteroatom-containing cycloaddition components is especially compelling, as such platforms enable streamlined access to heterocyclic frameworks that are prevalent throughout the pharmaceutical landscape. This Perspective provides an overview of ketenimine Diels–Alder chemistry and describes how this reactivity, together with the related chemistry of ketenes, has inspired our recent efforts to establish ketenimines as highly reactive aza-dienophiles.

Fields of Study & Subjects

Click Chemistry and Applications Advanced Synthetic Organic Chemistry Synthesis and Reactivity of Heterocycles

Publication details

Journal / source
Synlett
Publisher
Georg Thieme Verlag KG
Volume
37
Issue
14
Pages
1395–1400
Publication date
17 April 2026
Language
EN