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- W2053485709 abstract "The reduction of bicyclo[3.2.0]hept-3-en-6-ones 1a,b with Baker’s yeast to a mixture of enantiomerically pure (6S)-endo- and (6S)-exo-alcohols 2a,b and 3a,b respectively is described. Furthermore the oxidation of the racemic endo-alcohols 2a,b with Bacillus stearothermophilus afforded the corresponding ketones with high enantiomeric excesses resolving the endo-enantiomer. In the same conditions the exo-alcohols 3a,b are not oxidized." @default.
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- W2053485709 date "1996-07-01" @default.
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- W2053485709 title "Enantiomerically Pure 4-Methyl- and 1,4-Dimethyl-bicyclo[3.2.0]hept-3-en-6-ols and Ones by Microbial Redox" @default.
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- W2053485709 doi "https://doi.org/10.1246/cl.1996.511" @default.
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