1028277-45-3Relevant academic research and scientific papers
Stereochemistry of the Baker's Yeast Mediated Reduction of the C=C Bond of (Z)- and (E)-5-Benzoyloxyhex-3-en-2-one
Fronza, Giovanni,Fuganti, Claudio,Grasselli, Piero,Lanati, Simonetta,Rallo, Roberta,Tchilibon, Susanna
, p. 2927 - 2930 (2007/10/02)
Baker's yeast reduction of the Z and E enones 5 and 6 to the methyl ketone 7 proceeds with kinetic preference for the R and S enantiomers, respectively.However, irrespective of the double-bond stereochemistry and of the absolute configuration of the oxyge
