Enantioselective reduction of ortho-substituted acetophenones by bacterial strains isolated from medium enriched with biphenyl or diesel fuel was written by Andrade, Leandro H.;Comasseto, Joao V.;Rodrigues, Debora F.;Pellizari, Vivian H.;Porto, Andre L. M.. And the article was included in Journal of Molecular Catalysis B: Enzymatic in 2005.Recommanded Product: (S)-1-(2-Fluorophenyl)ethanol This article mentions the following:
Application of 21 new bacterial strains from natural environments (coastal plain of Santos and Atlantic Rain Forest, Sao Paulo, Brazil) in the asym. reduction of acetophenone derivatives is described. The bioreduction was carried out with whole bacterial cells leading to (S)-chiral alcs. in up to ≥99% e.e. The (S)-(-)-1-(2-bromophenyl)ethanol was employed in the preparation of chiral tellurium derivatives In the experiment, the researchers used many compounds, for example, (S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4Recommanded Product: (S)-1-(2-Fluorophenyl)ethanol).
(S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Recommanded Product: (S)-1-(2-Fluorophenyl)ethanol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts