|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|64645||48364||2016||5 صفحه PDF||سفارش دهید||دانلود کنید|
• High catalytic activity of palladium supported on polysiloxane microspheres in Suzuki reaction.
• High catalytic efficiency at low amount of Pd.
• Good selectivity to different substituted benzophenones at low CO pressure.
Carbonylative Suzuki–Miyaura cross-coupling reactions of various aryl iodides with phenylboronic acids were catalyzed by palladium supported on amino-modified silica microspheres. Reactions performed with a very low concentration of Pd, under the atmospheric pressure of CO, led to high/moderate yields of multiple benzophenones.
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Journal: Journal of Molecular Catalysis A: Chemical - Volume 417, June 2016, Pages 76–80