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Catalytic asymmetric cycloaddition of unsymmetrical EWG-activated alkenes to fully substituted pyrrolidines bearing three different carbonyl groups†
Shi-Lu Wu,Ning Li,Guan-Wu Yin,Zheng Xu,Fei Ye,Li Li,Yu-Ming Cui
Chemical Communications Pub Date : 11/05/2019 00:00:00 , DOI:10.1039/C9CC07738C
Abstract

A unique 1,3-dipolar [3+2] cycloaddition of alkyl 4-oxo-4-arylbut-2-enoates bearing two different electron-withdrawing groups was completed by using the silver/(R)-DTBM-Segphos catalyst system, which gives the corresponding fully substituted pyrrolidines with four stereogenic centers in good yields and with excellent enantioselectivities (up to 98% ee).

Graphical abstract: Catalytic asymmetric cycloaddition of unsymmetrical EWG-activated alkenes to fully substituted pyrrolidines bearing three different carbonyl groups
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