Chiral amine-urea mediated asymmetric inverse-electron-demand cycloadditions of cyclic nitrones with o-hydroxystyrenes

Abstract

Asymmetric inverse-electron-demand cycloaddition reactions of cyclic nitrones with o-hydroxystyrenes have been developed using a quinine-derived chiral amine-urea. The high levels of asymmetric induction are found to be afforded by an Anti-Open-S mechanism involving a dual activation system.

Graphical abstract: Chiral amine-urea mediated asymmetric inverse-electron-demand cycloadditions of cyclic nitrones with o-hydroxystyrenes

Supplementary files

Article information

Article type
Communication
Submitted
25 Dec 2025
Accepted
08 Jan 2026
First published
15 Jan 2026

Org. Biomol. Chem., 2026, Advance Article

Chiral amine-urea mediated asymmetric inverse-electron-demand cycloadditions of cyclic nitrones with o-hydroxystyrenes

Y. Toda, Y. Soma, N. Horiba, M. Koyama, F. Iwakuma, S. Matsumoto, K. Sukegawa, A. Kikuchi and H. Suga, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D5OB01989C

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