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Palladium complexes synthesis bearing

When the Pd bears chiral ligands, these reactions can be enantioselective.1448 ir-Allylmo-lybdenum compounds behave similarly.1449 Because palladium compounds are expensive, a catalytic synthesis, which uses much smaller amounts of the complex, was developed. That is, a substrate such as an allylic acetate, alcohol, amine, or nitro compound1450 is treated with the nucleophile, and a catalytic amount of a palladium salt is added. The rr-allylpal-ladium complex is generated in situ. Alkene-palladium complexes (introducing the nucleophile at a vinylic rather than an allylic carbon) can also be used.1451... [Pg.468]

The palladium-catalyzed amination of aryl halides has recently emerged as a powerful alternative to other methods for the synthesis of aryl amines.5 This method allows for the cross-coupling of aryl halides arrd triflates with amines in the presence of a stoichiometric amount of a base and catalytic amounts of palladium complexes bearing tertiary phosphine ligands. As shown in Tables I and II, the Pd/BlNAP catalyst is highly effective for reactions of aryl bromides and triflates with primary and cyclic... [Pg.15]

Kiely, D. and Guiry, PJ. (2003) Palladium complexes of phosphinamine ligands in the intramolecular asymmetric Heck reaction. Journal of Organometallic Chemistry, 687, 546-561. Dounary, A.B., Hatanaka, K., Kodanko, J.J. et al. (2003) Catalytic asymmetric synthesis of quaternary carbons bearing two aryl substituents. Enantioselective synthesis of 3-alkyl-3-aryl... [Pg.270]

Polystyrene is the most frequently used polymeric support for the immobilization of palladium complexes [15]. The PS resins are well developed in the field of sohd-phase peptide synthesis. Therefore resins bearing various chemical functional groups, diameter size, loading value, degree of cross-finking, for example, are now commercially readily available to permit investigation of these variables on the catalytic property. The most widely used polystyrene in... [Pg.79]

Synthesis of Palladium Complexes Bearing PXP-Pincer Ligands (X = Si, Ce, Sn)... [Pg.230]

Ort/ o-cyclometallated palladium complexes discussed in Section 2.2.2 have found another very important application as chiral templates that promote Diels-Alder and other reactions. This chemistry has been developed by Leung and co-workers and has allowed the synthesis of an impressing number of mono- and diphosphines bearing P-stereogenic atoms with peculiar scaffolds... [Pg.93]

Sanchez and coworkers reported the synthesis of palladium complexes bearing two imidazolin-2-ylidene moieties linked by a chiral dioxolane backbone (Figure 4.19). This is the first example on the use of a chiral bis(NHC)-metal catalyst in asymmetric hydrogenation with high enantioselectivity [60]. [Pg.122]

Buchwald and coworkers reported the synthesis of nitroarenes via coupling of aryl chlorides, triflates, and nonaflates with sodium nitrate [31]. Subsequently, palladium complex bearing Mor-DalPhos L57 has been utilized for the coupling of aryl chlorides and tosylates with hydrazines (Scheme 20.16) [32]. [Pg.555]


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Palladium complexes synthesis

Palladium synthesis

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