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  • Polymer CommunicationInfluence of cross-linking monomer and hydrophobic styrene comonomer on stereoselective esterase activities of polymer catalyst imprinted with a transition-state analogue for hydrolysis of amino acid esters

  • Add time:10/01/2019    Source:sciencedirect.com

    Polymer catalysts, cross-linked with N,N′-ethylene (C2) {or butylene (C4)}-bisacrylamide containing l-histidine and quaternary trimethylammonium groups were imprinted with a racemic transition-state analogue of phenyl 1-benzyloxycarbonyl-3-methylpentylphosphonate for the hydrolysis of p-nitrophenyl N-(benzyloxycarbonyl)-l (or d)-leucinate {Z-l (or d)-Leu-PNP}. Maximal stereoselectivity (l/d=8.4) was obtained by using N,N′-C4-bisacrylamide cross-linked polymer catalyst, which was copolymerized with hydrophobic styrene monomer.

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    Prev:Synthesis of multivalent carbonate esters by divergent growth of branched carbamates
    Next:Studies on amino acids and peptides—I : Synthesis of N-benzyloxycarbonylendo-thiodipeptide esters)

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