Issue 20, 2022

Copper(i)-catalyzed asymmetric [3 + 2] cycloaddition of N-ester acylhydrazones and β-trifluoromethyl-α,β-unsaturated ketones

Abstract

Herein, the first copper(I)-catalyzed asymmetric 1,3-dipolar [3 + 2] cycloaddition of N-ester acylhydrazones and β-trifluoromethyl-α,β-unsaturated ketones has been developed, affording an array of chiral pyrazolidine derivatives containing a trifluoromethyl moiety bearing three vicinal stereocenters in excellent yields with excellent enantioselectivities and diastereoselectivities (up to 96% yield, up to 97% ee and up to >20 : 1 dr). The chiral pyrazolidines could be transformed into 2-pyrazoline derivatives bearing a trifluoromethyl unit with excellent enantio- and diastereoselectivities. Moreover, the selected chiral pyrazolidines exhibited useful biological activities against human cancer cell lines.

Graphical abstract: Copper(i)-catalyzed asymmetric [3 + 2] cycloaddition of N-ester acylhydrazones and β-trifluoromethyl-α,β-unsaturated ketones

Supplementary files

Article information

Article type
Research Article
Submitted
21 Jun 2022
Accepted
19 Aug 2022
First published
22 Aug 2022

Org. Chem. Front., 2022,9, 5544-5550

Copper(I)-catalyzed asymmetric [3 + 2] cycloaddition of N-ester acylhydrazones and β-trifluoromethyl-α,β-unsaturated ketones

B. Zhu, H. Fan, Y. Ding, Y. Zhai, L. Wang, M. Wang, G. Zhu and J. Chang, Org. Chem. Front., 2022, 9, 5544 DOI: 10.1039/D2QO00993E

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