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Issue 2, 1991
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Enantioselective synthesis of the lactone moiety of the mevinic acids using D-xylose as a chiral precursor

Roberto Ballini,  Enrico Marcantoni  and  Marino Petrini 

Abstract

Homologation of the lactone 14 easily obtained from D-xylose afforded the pyranone 15, a key chiral synthon for the lactone portion of mevinic acids.

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Article type: Paper
DOI: 10.1039/P19910000490
Citation: J. Chem. Soc., Perkin Trans. 1, 1991,0, 490-491
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    Enantioselective synthesis of the lactone moiety of the mevinic acids using D-xylose as a chiral precursor

    R. Ballini, E. Marcantoni and M. Petrini, J. Chem. Soc., Perkin Trans. 1, 1991, 0, 490
    DOI: 10.1039/P19910000490

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