Taguchi analysis and asymmetric keto-reduction of acetophenone and its derivatives by soil filamentous fungal isolate: <i>Penicillium rubens</i> VIT SS1

Jothi, Saravanan; Vuppu, Suneetha

doi:10.1080/10826068.2020.1786697

Cited by 5 publications

(1 citation statement)

References 30 publications

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“…Asymmetric reduction reactions of prochiral ketones in anti ‐Prelog mode have been reported using whole cells of Acetobacter pasteurianus GIM1.158, [44] Leifsonia xyli HS0904, [45] Leifsonia xyli CCTCCM 2010241, [46] Lactobacillus reuteri DSM 20016, [47] and Penicillium citrinum VIT SS2, [48] and also when using the fungus Penicillium expansum [49] . The use of whole cells is attractive for several reasons, including production cost, space‐time‐yield and easier procedures [50,51] .…”

Section: Discussionmentioning

confidence: 99%

Alcohol Dehydrogenases with anti‐Prelog Stereopreference in Synthesis of Enantiopure Alcohols

Musa

2022

ChemistryOpen

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Biocatalytic production of both enantiomers of optically active alcohols with high enantiopurities is of great interest in industry. Alcohol dehydrogenases (ADHs) represent an important class of enzymes that could be used as catalysts to produce optically active alcohols from their corresponding prochiral ketones. This review covers examples of the synthesis of optically active alcohols using ADHs that exhibit anti ‐Prelog stereopreference. Both wild‐type and engineered ADHs that exhibit anti ‐Prelog stereopreference are highlighted.

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