A comparative  Suzuki reaction  of aryl halides using a new dimeric orthopalladated complex under conventional and microwave irradiation conditions | Zendy

Hajipour Abdol R. | Zendy; Karami Kazem | Zendy; Tavakoli Ghazal | Zendy

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A comparative Suzuki reaction of aryl halides using a new dimeric orthopalladated complex under conventional and microwave irradiation conditions

Author(s) -

Hajipour Abdol R.,

Karami Kazem,

Tavakoli Ghazal

Publication year - 2012

Publication title -

applied organometallic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.53

H-Index - 71

eISSN - 1099-0739

pISSN - 0268-2605

DOI - 10.1002/aoc.2852

Subject(s) - chemistry , phenylboronic acid , catalysis , aryl , potassium carbonate , halide , phosphine , microwave irradiation , coupling reaction , aryl halide , suzuki reaction , solvent , polymer chemistry , organic chemistry , photochemistry , palladium , alkyl

The cross‐coupling reaction between phenylboronic acid and various types of aryl halides ( Suzuki reaction ) was carried out using a catalytic amount of a new phosphine‐based catalyst under microwave irradiation. The reaction conditions were optimized and results showed that, by application of this catalytic system, N ‐methyl‐2‐pyrrolidone as the solvent and potassium carbonate as the base, reactions could be completed in a short reaction time with high to excellent yields. Copyright © 2012 John Wiley & Sons, Ltd.

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