4-Aminocyclopentenones were synthesized from readily available glycals and secondary anilines, with the aid of a Lewis acid–surfactant-combined catalyst. The reactions proceeded via a 4π conrotatory electrocyclization, affording the corresponding 4-aminocyclopentenones in good yields with excellent diastereoselectivities.
S. Wang, R. William, K. K. Georgina Estelle Seah and X. Liu, Green Chem., 2013, 15, 3180 DOI: 10.1039/C3GC41032C
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