氯化烯丙基钯(II)二聚体

Allylpalladium(II) chloride dimer is employed as catalyst in Heck reaction. It also participates as catalyst in the tandem nucleophilic allylation-alkoxyallylation reaction of the alkynylaldehydes with allyl chloride and allyltributylstannane.[] We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. These highly active catalyst complexes are used in Suzuki-Miyaura, Buchwald-Hartwig, and Heck reactions, enabling efficient C-C and C-N bond formation in sustainable synthesis, offering a greener, potentially more sustainable option for industrial chemical processes. Click here for more information.

Application Guide for Palladium Catalyzed Cross-Coupling Reactions Allylpalladium(II) chloride dimer has been employed for the following studies: Synthesis of cationic palladium cataysts, used in the microwave-assisted Heck arylation.[] Synthesis of N-heterocyclic carbene-palladium-η3-allyl chloride complexes, which are efficient catalyst for the Suzuki-Miyaura cross-coupling of aryl bromides and activated aryl chlorides.[] Synthesis of 1,4-diallyl-1,2-dihydroisoquinolines.[] As catalyst for greener Buchwald-Hartwig coupling in TPGS-750-M. On the Way Towards Greener Transition-Metal-Catalyzed Processes as Quantified by E Factors