The first heterogeneous Sonogashira coupling reaction of aryl halides with terminal alkynes catalyzed by diatomite-supported palladium(II) salophen complex

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Abstract

We report here our observation that, using appropriate reaction conditions, the Sonogashira reaction can be performed without the need for copper catalyst and solvent. Our approach involves the use of diatomite-supported palladium(II) salophen complex as a catalyst and triethylamine as a base. The methodology works, to differing extents, for aryl iodides and bromides. This heterogeneous catalyst can be reused at least five times without any decrease in activity. Copyright © 2011 John Wiley & Sons, Ltd.

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