Synthesis of Polycyclic Imidazolidinones via Cascade [3 + 2]-Annulation of β-Oxo-acrylamides with Cyclic <i>N</i>-Sulfonyl Imines
Lei Xie, Chenyi Zhao, Zhaoxue Wang, Zirui Chen, Yingying Zhao, Xinghan Liu, Xiangdong Xu, Wanxing Liu, Xiaojing Li, Lingang Wu
Abstract
An Et 3 N-catalyzed cascade [3 + 2]-annulation of β-oxo-acrylamides with cyclic N -sulfonyl ketimines or sulfamate-derived imines is developed under mild reaction conditions, which provides a concise and efficient route to access valuable sultam- or sulfamidate-fused imidazolidinone derivatives in good to excellent yields (80–95% yields) with excellent diastereoselectivities (>20:1 drs). The current protocol features atom economy, a transition-metal-free process, and broad functional group tolerance. Moreover, the asymmetric variant of the [3 + 2]-cycloaddition reaction was achieved in the presence of diphenylethanediamine or quinine-based bifunctional squaramide organocatalysts C-1 and C-11, giving the corresponding chiral polycyclic imidazolidinones in 68–90% yields with 25–94% ees and >20:1 drs in all cases.