Issue 23, 2019

Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives

Abstract

An efficient organocatalytic asymmetric formal [3 + 2] cycloaddition reaction of α-aryl isocyanoacetates with N-aryl or alkyl substituted itaconimides catalyzed by a dihydroquinine derived squaramide catalyst has been investigated, which affords the corresponding spiropyrroline succinimide derivatives with two non-adjacent quaternary–quaternary stereocenters in moderate to good yields (up to 82%) with moderate to excellent diastereoselectivities (up to >20 : 1 dr) and excellent enantioselectivities (90–>99% ee) under mild conditions.

Graphical abstract: Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
25 Jul 2019
Accepted
16 Oct 2019
First published
17 Oct 2019

Org. Chem. Front., 2019,6, 3879-3884

Organocatalyzed asymmetric formal [3 + 2] cycloaddition of isocyanoacetates with N-itaconimides: facile access to optically active spiropyrroline succinimide derivatives

M. Zhao, Q. Liu, K. Yu, X. Zhao and M. Shi, Org. Chem. Front., 2019, 6, 3879 DOI: 10.1039/C9QO00939F

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