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    Allylpalladium(II) chloride dimer is used as an important catalyst in Heck reaction.

    It reacts with cyclopentadienyl anion to give cyclopentadienyl allyl palladium.

    It acts as a precatalyst for asymmetric and cross-coupling catalysis.

    Further, it is used in the preparation of 1,4-diallyl-1,2-dihydroisoquinolines.

    It is also employed as a catalyst for greener Buchwald-Hartwig coupling reaction and involved in the synthesis of cationic palladium catalysts.

    In addition, it takes part in preparation of -heterocyclic carbene-palladium-eta3-allyl chloride complex,
    which is an efficient catalyst for the Suzuki-Miyaura cross-coupling reactions in synthetic chemistry.

     


    Nakayama, Y.; Yokoyama, N.; Nara, H.; Kobayashi, T.; Fujiwhara, M.
    An Efficient Synthesis of N-(Hetero)arylcarbazoles: Palladium-Catalyzed Coupling Reaction between (Hetero)aryl Chlorides and N-Carbazolylmagnesium Chloride. 
    Adv. Synth. Catal. 2015, 357 (10), 2322-2330.

     

    Chan, K. S. L.; Fu, H. Y.; Yu, J. Q.
    Palladium(II)-Catalyzed Highly Enantioselective C-H Arylation of Cyclopropylmethylamines. 
    J. Am. Chem. Soc. 2015, 137 (5), 2042-2046.

     

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