腈
环加成
化学
区域选择性
三氟甲基
烷基
肟
氯化物
组合化学
芳基
有机化学
药物化学
催化作用
作者
Bo Lin,Zipeng Zhang,Yunfei Yao,Yi You,Zhiqiang Weng
出处
期刊:Molecules
[MDPI AG]
日期:2022-10-04
卷期号:27 (19): 6568-6568
被引量:6
标识
DOI:10.3390/molecules27196568
摘要
We herein describe a general approach to 5-trifluoromethyl 1,2,4-triazoles via the [3 + 2]-cycloaddition of nitrile imines generated in situ from hydrazonyl chloride with CF3CN, utilizing 2,2,2-trifluoroacetaldehyde O-(aryl)oxime as the precursor of trifluoroacetonitrile. Various functional groups, including alkyl-substituted hydrazonyl chloride, were tolerated during cycloaddition. Furthermore, the gram-scale synthesis and common downstream transformations proved the potential synthetic relevance of this developed methodology.
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