Issue 34, 2022

Synthesis of 1,3,5-trisubstituted pyrazoles via 1,3-dipolar cycloaddition of nitrile imines with ninhydrin-derived Morita–Baylis–Hillman carbonates

Abstract

An effective synthetic method for 1,3,5-trisubstituted pyrazoles via 1,3-dipolar cycloaddition reaction has been developed. This reaction could smoothly proceed between ninhydrin-derived Morita–Baylis–Hillman carbonates and nitrilimines to provide a wide scope of differently substituted pyrazoles in high yields (up to 95%). In addition, the reaction mechanism was also proposed to explain its regioselectivity.

Graphical abstract: Synthesis of 1,3,5-trisubstituted pyrazoles via 1,3-dipolar cycloaddition of nitrile imines with ninhydrin-derived Morita–Baylis–Hillman carbonates

Supplementary files

Article information

Article type
Paper
Submitted
13 Jul 2022
Accepted
08 Aug 2022
First published
08 Aug 2022

Org. Biomol. Chem., 2022,20, 6923-6930

Synthesis of 1,3,5-trisubstituted pyrazoles via 1,3-dipolar cycloaddition of nitrile imines with ninhydrin-derived Morita–Baylis–Hillman carbonates

K. Wang, Y. Li, J. Jing, R. Chen, N. Zhao, Z. Li, M. Wang and S. Ji, Org. Biomol. Chem., 2022, 20, 6923 DOI: 10.1039/D2OB01253G

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