Abstract:The coupling reaction of phenylboronic acid with 4-silyl-bromobenzenes incorporating an ionic liquid support or its neutral analogue at 80 °C in DMF/H 2 O in the presence of Pd(PPh 3 ) 4 and Na 2 CO 3 takes place much faster and more efficiently under microwave irradiation than under traditional heating. It is an attractive method to carry out the generally slow Suzuki-Miyaura reactions under microwave conditions.
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