Whole Cells Mediated Biocatalytic Reduction of Alpha- Keto Esters: Preparation of Optically Enriched Alkyl 2-hydroxypropanoates
DOI:
https://doi.org/10.5530/ctbp.2022.2s.37Keywords:
Asymmetric reduction, Alkyl 2-oxopropanoates, Alpha-keto esters, Candida parapsilosis, Ethyl 3-bromo-2- oxopropanoate IntroductionAbstract
Biocatalytic reduction of alkyl 2-oxopropanoates were carried out by utilizing the whole cells of Candida parapsilosis ATCC 7330 to form the optically enriched alkyl 2-hydroxypropanoates with good enantiomeric excess (ee) (≤91%) and isolated yields (≤68%). Enantiomerically enriched (S)-ethyl 3-bromo-2- hydroxypropanoate thus synthesized by biocatalytic reduction of ethyl 3-bromo- 2-oxopropanoate is presented in this study for the first time in water under ambient reaction conditions in a reaction time of 4 h which is considerably less than earlier reported procedures.