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Biocatalysis: Synthesis of Key Intermediates for Development of Pharmaceuticals

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ACS CATALYSIS
卷 1, 期 9, 页码 1056-1074

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AMER CHEMICAL SOC
DOI: 10.1021/cs200219b

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biocatalysis; enantioselective; regioselective; reduction; transamination; deracemization; reductive amination; desymmetrization; resolution; chiral drug intermediates

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Chirality is a key factor for the safety and efficacy of many drug products. The production of single enantiomers of drug intermediates has become increasingly important in the pharmaceutical industry. There has been an enormous potential of microorganisms and enzymes derived from there for the transformation of synthetic chemicals with high chemo-, regio-, and enatioselectivities. Recent development in the area of directed evolution has led screen mutants under process conditions to increase activity and selectivity of biocatalysts, thus making the enzymatic process highly efficient and economically feasible. In this review, chemoenzymatic processes are described for the synthesis of chiral intermediates for the development of pharmaceuticals.

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