Issue 16, 2021

Organocatalytic asymmetric formal [3 + 2] cycloaddition reaction of isocyanoacetates with saccharin-derived 1-azadienes

Abstract

An efficient organocatalytic diastereo- and enantioselective formal [3 + 2] cycloaddition reaction of α-isocyanoacetates with saccharin-derived 1-azadienes catalyzed by a dihydroquinine derived squaramide catalyst has been investigated, and it furnished the corresponding directly linked benzo[d]isothiazole 1,1-dioxide-dihydropyrroles with two adjacent tertiary-quaternary stereocenters in high yields (up to 98%), with moderate to excellent stereoselectivities (up to >20 : 1 dr and 97% ee) under mild conditions.

Graphical abstract: Organocatalytic asymmetric formal [3 + 2] cycloaddition reaction of isocyanoacetates with saccharin-derived 1-azadienes

Supplementary files

Article information

Article type
Paper
Submitted
22 Jan 2021
Accepted
23 Mar 2021
First published
25 Mar 2021

Org. Biomol. Chem., 2021,19, 3687-3697

Organocatalytic asymmetric formal [3 + 2] cycloaddition reaction of isocyanoacetates with saccharin-derived 1-azadienes

L. Chang, G. Zhu, T. Yang, X. Zhao, M. Shi and M. Zhao, Org. Biomol. Chem., 2021, 19, 3687 DOI: 10.1039/D1OB00115A

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