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

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

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra03000e
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

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

Khurshed A. Bozorov, Buer Song, Wei Liu, Xueqing Zhang et al.
1 citations
RSC Advances
Fluorine in Organic Chemistry
0.79
article

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

Khurshed A. Bozorov, Buer Song, Wei Liu, Xueqing Zhang, Yanhui Zhao
article en
1 citations

Abstract

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

RSC AdvancesVol. 15(24)
Samarkand State University named after Sharof Rashidov (UZ), Yili Normal University (CN)
Clean water and sanitation
Openalex Percentile: Top 27%
Fluorine in Organic Chemistry
0.79
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