Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/8754
Title: Studies on phosphine free Pd-salen complexes as effective catalysts for aqueous Suzuki reaction
Authors: Borhade, Sanjay R
Waghmode, Suresh B
Keywords: Suzuki reaction
biaryls
Pd-salen
phosphine-free
aryl boronic acid
Issue Date: May-2010
Publisher: CSIR
Abstract: <smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="metricconverter"> Palladium complexes of the salen ligands, <i style="">N</i>,<i style="">N</i>'-bis(salicylidene)-ethylenediamine and <i style="">N</i>,<i style="">N</i>'-bis(salicylidene)-1,2-phenylenediamine have been explored for their catalytic activity in a<b style=""> </b>phosphine-free aqueous Suzuki reaction. The various reaction parameters have been systematically optimized with respect to various solvents, bases, temperatures and Pd concentrations. The studies conclude that 1:1 DMF to water solvent ratio, Na<sub>2</sub>CO<sub>3 </sub>as base and 0.5 mol% of palladium at 90°C is apt for Suzuki reactions. Rapid transformation of substituted aryl iodides and aryl bromides into corresponding biaryls has been observed with excellent yield ranging from 70-86%, under optimized conditions. </smarttagtype>
Description: 565-572
URI: http://hdl.handle.net/123456789/8754
Appears in Collections:IJC-B Vol.49B(05) [May 2010]

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