|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|64533||48361||2016||8 صفحه PDF||سفارش دهید||دانلود کنید|
The use of copper selenide nanocatalyst for an efficient and regioselective cross-dehydrogenative coupling (CDC) of tertiary amines with terminal alkynes in the presence of tert-butyl hydroperoxide as the oxidant is demonstrated for the first time. The catalyst comprising of unique Cu6Se4.5 nanoparticles synthesized from a single source precursor CuSePh, is required in much lower amount (1 mol%), and is recyclable up to four reaction cycles with slight loss in activity. The reaction can be executed in the absence of solvent, is applicable to aromatic, benzylic, and aliphatic tertiary amines, and furnishes propargylamines in moderate to good yields.
Cu6Se4.5 NPs, synthesized for the first time from a SSP are efficient and reusable catalyst for synthesis of propargylamines under solvent-free conditions.Figure optionsDownload high-quality image (71 K)Download as PowerPoint slide
Journal: Journal of Molecular Catalysis A: Chemical - Volume 423, November 2016, Pages 135–142