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Synthetic Route of 84127-04-8, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 84127-04-8, C14H15O2P. A document type is Patent, introducing its new discovery.

The present invention relates to a P chiral pincer compound (II) and a palladiumcoordination compound (I) thereof, and synthesis methods of the two compounds. According to the present invention, the palladium coordination compound (I) (wherein X represents -Cl, R represents hydrogen atom or C1-C4 alkyl, and the chiralities of the two P are simultaneously R configurations or S configurations) is synthesized through a coordination reaction of the compound (II) and a divalent palladium salt; the palladium coordination compound (I) (wherein X is selected from -Br, -I, -OAc, -OTf, -BF4 and -SbF6) is synthesized through an anion exchange reaction of the palladium coordination compound (I) with the X represented by -Cl; and the palladium coordination compound (I) of the present invention can be adopted as the chiral catalyst so as to be used in a variety of asymmetric reactions such as asymmetric Micheal addition, asymmetric Heck coupling reactions, asymmetric Suzuki-Miyaura coupling reactions, asymmetric allylation reactions and the like. The formulas (I) and (II) are defined in the instruction.

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Reference:
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate