Mechanistic and synthetic aspects of hydroboration with a simple atropisomeric ligand prepared from 1-(1′-isoquinolyl)-2-naphthol was written by Korostylev, Andrei;Gridnev, Ilya;Brown, John M.. And the article was included in Journal of Organometallic Chemistry in 2003.Reference of 171032-87-4 This article mentions the following:
A novel triaryl phosphite ligand was prepared directly from both enantiomers of BINOL and a single enantiomer of 1-(1′-isoquinolyl)-2-naphthol. In one of the two cases the cationic Rh complex proved to be reasonably effective in the asym. hydroboration of electron-poor styrenes. It was possible to identify binuclear reactive intermediates when the hydroboration pre-catalyst was examined in the presence of catecholborane at low temperatures In the experiment, the researchers used many compounds, for example, (S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4Reference of 171032-87-4).
(S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Reference of 171032-87-4
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts