Regioselective hydrosilylation of epoxides catalysed by nickel(II) hydrido complexes was written by Wenz, Jan;Wadepohl, Hubert;Gade, Lutz H.. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2017.Formula: C9H9F3O This article mentions the following:
Bench-stable nickel fluoride complexes bearing chiral substituted bis(oxazolinylisopropylidene)pyrrole NNN-pincer ligands were employed as precursors for the regioselective hydrosilylation of epoxides at room temperature A nickel hydride assisted epoxide opening is followed by the cleavage of the newly formed Ni-O bond by σ-bond metathesis with a silane. In the experiment, the researchers used many compounds, for example, 2-(4-(Trifluoromethyl)phenyl)ethanol (cas: 2968-93-6Formula: C9H9F3O).
2-(4-(Trifluoromethyl)phenyl)ethanol (cas: 2968-93-6) 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. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Formula: C9H9F3O
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts