615556-87-1Relevant academic research and scientific papers
Enantiomerically Pure Octahydronaphthalenone and Octahydroindenone: Elaboration of the Substrate Overcame the Specificity of Yeast-Mediated Reduction
Fuhshuku, Ken-Ichi,Tomita, Mina,Sugai, Takeshi
, p. 766 - 774 (2003)
Substrate specificity on the reduction of bicyclic diketones with a yeast strain, Torulaspora delbrueckii IFO10921, was investigated. Although this yeast efficiently reduces the isolated carbonyl group involved in the (S)-enantiomer of Wieland-Miescher ke
