首页> 外文期刊>Journal of Fluorine Chemistry >Scope and regioselectivity of the 1,3-dipolar cycloaddition of azides with methyl 2-perfluoroalkynoates for an easy, metal-free route to perfluoroalkylated 1,2,3-triazoles
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Scope and regioselectivity of the 1,3-dipolar cycloaddition of azides with methyl 2-perfluoroalkynoates for an easy, metal-free route to perfluoroalkylated 1,2,3-triazoles

机译:叠氮化物与2-全氟炔酸甲酯的1,3-偶极环加成反应的范围和区域选择性,可轻松,无金属地制得全氟烷基化1,2,3-三唑

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摘要

1,3-Dipolar cycloadditions of methyl 2-perfluoroalkynoates with various azides have been examined, leading to a simple metal-free synthetic protocol for the synthesis of perfluoroalkylated 1,2,3-triazoles. The regiochemical results demonstrated that the cycloaddition was controlled by FMO (the frontier molecular obitals) interaction and steric hindrance in transition states.
机译:已研究了2-全氟链烷酸甲酯与各种叠氮化物的1,3-偶极环加成反应,从而导致了用于合成全氟烷基化的1,2,3-三唑的简单的无金属合成方案。区域化学结果表明,在过渡态中,环加成反应受FMO(前沿分子小分子)相互作用和空间位阻的控制。

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