Issue 35, 2022

Catalytic asymmetric [3 + 2] cycloaddition of pyrazolone-derived MBH carbonate: highly stereoselective construction of the bispiro-[pyrazolone-dihydropyrrole-oxindole] skeleton

Abstract

A catalytic asymmetric construction of the bispiro[pyrazolone–dihydropyrrole–oxindole] skeleton catalyzed by chiral DMAP-derived catalyst was successfully achieved by employing recently explored pyrazolone-derived MBH carbonate in high yields with excellent stereoselectivities. The proposed transition state indicated that the intermolecular hydrogen bonds and π–π interactive forces played an essential role in stereoselective chemical transformation.

Graphical abstract: Catalytic asymmetric [3 + 2] cycloaddition of pyrazolone-derived MBH carbonate: highly stereoselective construction of the bispiro-[pyrazolone-dihydropyrrole-oxindole] skeleton

Supplementary files

Article information

Article type
Communication
Submitted
30 Jan 2022
Accepted
04 Apr 2022
First published
12 Apr 2022

Chem. Commun., 2022,58, 5363-5366

Catalytic asymmetric [3 + 2] cycloaddition of pyrazolone-derived MBH carbonate: highly stereoselective construction of the bispiro-[pyrazolone-dihydropyrrole-oxindole] skeleton

Z. Tian, J. Jiang, Z. Yan, Q. Luo, G. Zhan, W. Huang, X. Li and B. Han, Chem. Commun., 2022, 58, 5363 DOI: 10.1039/D2CC00618A

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