Alcohol dehydrogenases are a well-known group of enzymes in the class of
oxidoreductases that use electron transfer cofactors such as NAD (P)+/NAD (P) H for …

Abstract (S)-2-Chloro-1-(3, 4-difluorophenyl)-ethanol [(S)-CFPL] is a key chiral intermediate
in the manufacture of Ticagrelor. In this study, deep eutectic solvent (DES) was used as the …

Biocatalyzed asymmetric reduction of ketones is one of the most cost-effective and
environmentally friendly approaches for preparing chiral alcohols. However, few natural …

Microbial biotransformation is valuable for obtaining pharmaceutical, nutritional, and
cosmetical potential molecules. Basically, for its realization, only a parental molecule, a …

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 …

Asymmetric bioreduction catalyzed by biocatalyst have shown considerable potential in the
preparation of chiral alcohols.(R)-1-(furan-2-yl) ethanol ((R)-2) can be used precursor in the …

Asymmetric bioreduction of ketones is a fundamental process in the production of organic
molecules. Compounds containing tetralone rings are found in the structure of many …

There is a considerable interest in the asymmetric production of chiral allylic alcohols, the
main building blocks of many functional molecules. The asymmetric reduction of α, β …

Optically active aromatic alcohols are valuable chiral building blocks of many natural
products and chiral drugs. Lactobacillus paracasei BD87E6, which was isolated from a …

Whole-cell biocatalysts have been a popular method for the preparation of chiral alcohols.
Although asymmetric reduction of cyclohexyl (phenyl) methanone (1) by chemical catalysts …