Enantioselective synthesis of both enantiomers of dimethyl cis-(4-acetoxycyclopent-2-enyl)malonate, key intermediates for epijasmonate

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Abstract

Both enantiomers (3 and 4) of dimethyl cis-(4-acetoxycyclopent-2-enyl)malonate (3), known intermediates for the synthesis of epijasmonate, were prepared in an enantio-enriched form from common starting material 2 based on desymmetrization of the meso-character by palladium-catalyzed asymmetric allylic alkylation. © 2002 by Japan Society for Bioscience, Biotechnology, and Agrochemistry.

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Tanimori, S., Tsuji, Y., & Kirihata, M. (2002). Enantioselective synthesis of both enantiomers of dimethyl cis-(4-acetoxycyclopent-2-enyl)malonate, key intermediates for epijasmonate. Bioscience, Biotechnology and Biochemistry, 66(3), 660–662. https://doi.org/10.1271/bbb.66.660

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