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Issue 7, 1991
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Hydrolytic and reductive action of fermenting yeast on a keto acetate: synthesis of (+)-endo-brevicomin

Abstract

The keto acetate 1 in fermenting yeast gives the diol 2 with high enantiomeric excess. The product arises from hydrolysis–reduction and is transformed into (+)-endo-brevicomin. The hydroxy acetate from direct reduction of 1 is racemic.

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Article type: Paper
DOI: 10.1039/P19910001764
Citation: J. Chem. Soc., Perkin Trans. 1, 1991,0, 1764-1765
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    Hydrolytic and reductive action of fermenting yeast on a keto acetate: synthesis of (+)-endo-brevicomin

    G. Pedrocchi-Fantoni and S. Servi, J. Chem. Soc., Perkin Trans. 1, 1991, 0, 1764
    DOI: 10.1039/P19910001764

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