Issue 2, 1991
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

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 information

DOI
https://doi.org/10.1039/P19910000490
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 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, 490 DOI: 10.1039/P19910000490

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