Construction of 2‐(Trifluoromethyl)‐[1,2,4]Triazolo[1,5‐<i>a</i>]Quinoline Derivatives via Cycloaddition of <i>N</i>‐Amino Quinolinium Salts with CF<sub>3</sub>CN

Abstract A (3+2)‐cycloaddition of N ‐amino quinolinium salts with in situ generated trifluoroacetonitrile is disclosed. The reaction affords access to structurally diverse 2‐(trifluoromethyl)‐[1,2,4]triazolo[1,5‐ a ]quinoline derivatives in good yields, utilizing 2,2,2‐trifluoroacetaldehyde O ‐(aryl)oxime as precursor of trifluoroacetonitrile.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-02-18
DOI
https://doi.org/10.1002/ajoc.202500010
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

Construction of 2‐(Trifluoromethyl)‐[1,2,4]Triazolo[1,5‐a]Quinoline Derivatives via Cycloaddition of N‐Amino Quinolinium Salts with CF3CN

Shouxiong Chen, Zhiqiang Weng, Fafu Yang, Peiqi Yang et al.
1 citations
Asian Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.79
article

Construction of 2‐(Trifluoromethyl)‐[1,2,4]Triazolo[1,5‐a]Quinoline Derivatives via Cycloaddition of N‐Amino Quinolinium Salts with CF3CN

Shouxiong Chen, Zhiqiang Weng, Fafu Yang, Peiqi Yang, Z. Chen
article en
1 citations

Abstract

Abstract A (3+2)‐cycloaddition of N ‐amino quinolinium salts with in situ generated trifluoroacetonitrile is disclosed. The reaction affords access to structurally diverse 2‐(trifluoromethyl)‐[1,2,4]triazolo[1,5‐ a ]quinoline derivatives in good yields, utilizing 2,2,2‐trifluoroacetaldehyde O ‐(aryl)oxime as precursor of trifluoroacetonitrile.

Asian Journal of Organic ChemistryVol. 14(5)
Fujian Normal University (CN), Minjiang University (CN), Fuzhou University (CN)
Openalex Percentile: Top 31%
Fluorine in Organic Chemistry
0.79
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