Asymmetric reduction of halo-substituted arylalkanones with Rhizopus arrhizus was written by Salvi, Neeta A.;Chattopadhyay, Subrata. And the article was included in Tetrahedron: Asymmetry in 2008.HPLC of Formula: 171032-87-4 This article mentions the following:
The Rhizopus arrhizus-mediated asym. reduction of various haloaryl alkanones furnished the resp. (S)-carbinols, e.g., I, with good to excellent enantioselectivities. It was found that the reaction course was primarily governed by the relative position of the halogen with respect to the carbonyl group, and its size. The relative order of efficacies of the nature of the halogen and their substitution pattern were Br > Cl > F and o- > p- > m-. The ortho-effect was the most predominant factor in the stereochem. outcome of the reaction, which was also confirmed with some non-halo-substituted acetophenones. 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. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 171032-87-4
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts