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Synthesis of 1,3,5-trisubstituted pyrazoles via 1,3-dipolar cycloaddition of nitrile imines with ninhydrin-derived Morita–Baylis–Hillman carbonates†
Kai-Kai Wang,Yan-Li Li,Jun Jing,Rongxiang Chen,Na-Na Zhao,Zhi-Hui Li,Ming-Yue Wang,Shuo-Ke Ji
Organic & Biomolecular Chemistry Pub Date : 08/08/2022 00:00:00 , DOI:10.1039/D2OB01253G
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
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