首页> 外文期刊>Journal of the Brazilian Chemical Society >Synthesis of 3-(1H-1,2,3-Triazol-1-yl)-2-(arylselanyl)pyridines by Copper-Catalyzed 1,3-Dipolar Cycloaddition of 2-(Arylselanyl)-3-azido-pyridines with Terminal Alkynes
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Synthesis of 3-(1H-1,2,3-Triazol-1-yl)-2-(arylselanyl)pyridines by Copper-Catalyzed 1,3-Dipolar Cycloaddition of 2-(Arylselanyl)-3-azido-pyridines with Terminal Alkynes

机译:铜催化带有末端末端的2-(芳基杂戊基)-3-叠氮基吡啶的1,3-偶极环加成反应,合成3-(1H-1,2,3-三唑-1-基)-2-(芳基杂戊基)吡啶炔烃

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We present here our results in the synthesis of eleven new 3-(1H-1,2,3-triazol-1-yl)-2-(arylselanyl)pyridines by copper-catalyzed azide-alkyne cycloaddition reactions. The reactions were performed in the presence of catalytic amount of copper(II) acetate and sodium ascorbate using a mixture of tetrahydrofuran/water (1:1) as solvent at room temperature in air. The reaction is tolerant to different functional groups such as substituted-benzene rings, alcohol and ester and none electronic or steric influence was observed. All the products were obtained in good to excellent yields. Alternatively to the conventional oil bath heating, the use of microwave irradiation or ultrasound methods is also presented as alternative energy sources.
机译:在这里,我们通过铜催化的叠氮化物-炔烃环加成反应合成11个新的3-(1H-1,2,3-三唑-1-基)-2-(芳基亚硒基)吡啶。反应在催化量的乙酸铜(II)和抗坏血酸钠存在下,在室温下在空气中使用四氢呋喃/水(1:1)的混合物作为溶剂进行。该反应耐受不同的官能团,例如取代的苯环,醇和酯,并且没有观察到电子或空间影响。所有产品均以良好至极好的收率获得。作为常规油浴加热的替代方法,还提出了使用微波辐射或超声方法作为替代能源。

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