Bioconversion of acetophenones by marine fungi isolated from marine algae Bostrychia radicans and Sargassum sp. was written by Mouad, Ana Maria;Martins, Mariana Provedel;Romminger, Stelamar;Seleghim, Mirna Helena Regali;Leandrini de Oliveira, Ana Ligia;Debonsi, Hosana Maria;Yokoya, Nair Sumie;Fujii, Mutue Toyota;Passarini, Michel Rodrigo Zambrano;Bonugli-Santos, Rafaella Costa;Sette, Lara Duraes;Porto, Andre Luiz Meleiro. And the article was included in Current Topics in Biotechnology in 2012.HPLC of Formula: 171032-87-4 This article mentions the following:
The bioconversion of acetophenone derivatives 1-6 was investigated using whole cells of marine fungi Botryosphaeria sp. Br-09, Eutypella sp. Br-023, Hydropisphaera sp. Br-27 and Xylaria sp. Br-61 isolated from the red alga Bostrychia radicans and Arthopyrenia sp. SGPY-41, Penicillium sp. SMA2-8, Pestalotiopsis sp. SMA2-C isolated from brown alga Sargassum sp. Asym. reduction produced the enantiopure (R)- or (S)-alcs. 7-12 with high enantiomeric excess (>99 % ee). This study describes the first investigation with marine-derived fungi recovered from algae for biocatalytic reduction The fungus Botryosphaeria sp. Br-09 showed excellent reductions for ortho-acetophenone derivatives 1-6. In the experiment, the researchers used many compounds, for example, (S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4HPLC of Formula: 171032-87-4).
(S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.HPLC of Formula: 171032-87-4
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts