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首页> 外文期刊>Current Microwave Chemistry >Microwave Assisted Rapid Synthesis of (Arylselanyl)phenyl-1H-1,2,3- triazoles by Copper Catalyzed 1,3-Dipolar Cycloaddition
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Microwave Assisted Rapid Synthesis of (Arylselanyl)phenyl-1H-1,2,3- triazoles by Copper Catalyzed 1,3-Dipolar Cycloaddition

机译:铜催化的1,3-偶极环加成反应微波辅助快速合成(芳基戊基)苯基-1H-1,2,3-三唑

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We describe here a simple and rapid protocol for the synthesis of (arylselanyl)phenyl-1H- 1,2,3-triazoles by copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions using Microwave Irradiation. The products were obtained under mild conditions in excellent yields in a short reaction time by reacting azidophenyl arylselenides with a range of terminal alkynes using catalytic amount of Cu(OAc)_2.H_2O/sodium ascorbate. This Click Chemistry protocol is an efficient method to synthesize new selenium compounds with potential application in biological studies and materials sciences.
机译:我们在这里描述了一种简单快速的方案,用于通过使用微波辐射的铜催化的叠氮化物-炔烃环加成(CuAAC)反应来合成(芳基硒基)苯基-1H-1,2,3-三唑。通过使用催化量的Cu(OAc)_2.H_2O /抗坏血酸钠使叠氮苯基芳基硒化物与一定范围的末端炔烃反应,在温和条件下以短时间获得优异的收率。该Click Chemistry规程是一种合成新硒化合物的有效方法,在生物学研究和材料科学中具有潜在的应用前景。

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