Biocatalytic asymmetric reduction of prochiral bulky-bulky ketones is an attractive approach
to produce their corresponding valuable enantiopure alcohols. These ketones contain alkyl …

Studies in Natural Products Chemistry, Volume 79 covers the synthesis, testing and
recording of the medicinal properties of natural products, providing cutting-edge accounts of …

Secondary metabolites that can be produced from primary ones are not directly involved in
the normal growth, development, and reproduction of the organism. They are molecules that …

Enantiomerically pure (R)-β-hydroxy-1, 2, 3-triazole derivatives, which are important β-
blocker analogues, have been synthesized by exploiting an unusual Prelog enantioselective …

Aryl and heteroaryl chiral carbinols are useful precursors in the synthesis of drugs.
Lactobacillus paracasei BD87E6, which is obtained from a cereal based fermented …

Asymmetric bioreduction of aromatic and heteroaromatic ketones is an important process in
the production of precursors of biologically active molecules. In this study, the bioreduction …

Optically active alcohols are crucial precursors. 1, 2-Diarylethanols and their analogues
constitute a significant group of substances of biological significance. The biocatalytic …

Biocatalytic asymmetric reduction of ketone is an efficient method for the production of chiral
carbinols. The study indicates selective bioreduction of different ketones (1–8) to their …

Yeast cells are popular microorganisms for use in various bioprocesses because of their
ability to produce various enzymes. They are also known for their low price. However, the …

Microbial asymmetric reduction of ketone is an efficient tool for the synthesis of chiral
alcohols. This research focuses on exploring the soil fungal isolates for their ability toward …