Issue 24, 2025

[4 + 2] Cycloaddition of α-bromotrifluoromethylhydrazone with alkenes: synthesis of trifluoromethyltetrahydropyridazines

Abstract

A catalyst-free [4 + 2] cyclization process between trifluoromethyl-containing 1,2-diazabuta-1,3-diene and simple olefins was developed by in situ generation. Under mild conditions, trifluoromethyl-containing 1,4,5,6-tetrahydropyridazine compounds were obtained, in high yields (up to 96% yields).

Graphical abstract: [4 + 2] Cycloaddition of α-bromotrifluoromethylhydrazone with alkenes: synthesis of trifluoromethyltetrahydropyridazines

Supplementary files

Article information

Article type
Paper
Submitted
09 May 2025
Accepted
03 Jun 2025
First published
09 Jun 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 19417-19420

[4 + 2] Cycloaddition of α-bromotrifluoromethylhydrazone with alkenes: synthesis of trifluoromethyltetrahydropyridazines

Y. Zhao, H. Rong, K. Bozorov, X. Zhang, B. Song and W. Liu, RSC Adv., 2025, 15, 19417 DOI: 10.1039/D5RA03000E

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