Asymmetric C-C bond formation with L-prolinol derived chiral catalysts immobilized on polymer fibers

S Degni, CE Wilen, Reko Leino

    Research output: Contribution to journalArticleScientificpeer-review

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    Abstract

    N-(4-Vinylbenzyl)-alpha,alpha-diphenyl-L-prolinol was immobilized on polyethylene fibers by electron beam induced pre-irradiation grafting using styrene as a co-monomer. The resulting polymer supported catalyst P2 was utilized in asymmetric C-C bond forming reactions and its performance compared with those of previously prepared fibrous cross-linked alpha,alpha-diphenyl-L-prolinol P1 and homogeneous model compounds. The fibrous catalyst yields similar enantioselectivities in the asymmetric addition of diethylzinc to benzaldehyde as its homogeneous reference reaction and can be recycled with minimal loss of activity. When P2 was used as the catalyst in the addition of phenylacetylene to benzaldehyde, the corresponding propargylic alcohol was obtained with enantiomeric excesses of up to 91%. (C) 2003 Published by Elsevier Ltd.
    Original languageUndefined/Unknown
    Pages (from-to)231–237
    Number of pages7
    JournalTetrahedron: Asymmetry
    Volume15
    Issue number2
    DOIs
    Publication statusPublished - 2004
    MoE publication typeA1 Journal article-refereed

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