Palladium catalysis in water: Design, preparation, and use of amphiphilic resin-supported palladium-phosphine complexes

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Abstract

Palladium-catalyzed synthetic transformations (πallylic substitution, carbonylation. cross-coupling, etc.) were achieved in water by use of amphiphilic polystyrene-poly(ethylene glycol) resin (PS-PEG)-supported palladium-phosphine complexes. Asymmetric allylic alkylation of cyclic ullyl esters was catalyzed by a palladium complex of a PS-PEG-supponed chiral (imidazoindole)phosphine ligand with high enantioselectivity of up to 99% ee.

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Uozumi, Y. (2002). Palladium catalysis in water: Design, preparation, and use of amphiphilic resin-supported palladium-phosphine complexes. Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 60(11 SPEC.), 1063–1068. https://doi.org/10.5059/yukigoseikyokaishi.60.1063

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