Issue 78, 2016

Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones

Abstract

A highly diastereo- and enantioselective [3+2] cycloaddition reaction of N-2,2,2-trifluoroethylisatin ketimines and 3-alkenyl-5-arylfuran-2(3H)-ones was developed with 1 mol% thiourea–tertiary amine as the catalyst. A series of spiro[pyrrolidin-3,2′-oxindoles] bearing four consecutive stereocenters, including two vicinal spiro-quaternary chiral centers, were efficiently obtained with excellent results (up to >99% yield, >20 : 1 dr, and >99% ee).

Graphical abstract: Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones

Supplementary files

Article information

Article type
Communication
Submitted
01 Aug 2016
Accepted
02 Sep 2016
First published
02 Sep 2016

Chem. Commun., 2016,52, 11708-11711

Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones

Z. Wang, Z. Wu, D. Yue, W. Hu, X. Zhang, X. Xu and W. Yuan, Chem. Commun., 2016, 52, 11708 DOI: 10.1039/C6CC06367E

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