Origin of the unexpected enantioselectivity in the enzymatic reductions of 5-membered-ring heterocyclic ketones catalyzed by candida parapsilosis carbonyl reductases

HIGHLIGHTS

• who: Byu Ri Sim et al. from the State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China have published the paper: Origin of the Unexpected Enantioselectivity in the Enzymatic Reductions of 5-Membered-Ring Heterocyclic Ketones Catalyzed by Candida parapsilosis Carbonyl Reductases, in the Journal: Catalysts 2022, 12, x FOR PEER REVIEW of 25/07/2022
• what: The authors reported an unexpected enantioselectivity in the enzyme reductions of dihydrofuran-3(2H)-one (DHF) to (S)-tetrahydrofuran-3 . . .
  

   

  

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