Name: (3-Fluorophenyl)boronic acidIn 2019 ,《New approach to unsymmetrical 1,3-diazatriphenylenes through intramolecular oxidative cyclodehydrogenation》 appeared in Tetrahedron. The author of the article were Verbitskiy, Egor V.; Eltsov, Oleg S.; Zhilina, Ekaterina F.; Pakhomov, Ilya M.; Rusinov, Gennady L.; Chupakhin, Oleg N.; Charushin, Valery N.. The article conveys some information:
An efficient synthetic route towards previously inaccessible dibenzo[f,h]quinazolines and [1]benzothieno[3,2-f]benzo[h]quinazolines through FeCl3-mediated intramol. oxidative cyclodehydrogenation of readily available 5-([1,1′-biphenyl]-2-yl)pyrimidines and 5-(2-phenylbenzo[b]thiophen-3-yl)pyrimidines was described. MO calculations (DFT), as well as redox and photophys. measurements for all new compounds was performed. The data showed that the reported polycyclic systems have a potential to use in organic electronic applications. In the experiment, the researchers used many compounds, for example, (3-Fluorophenyl)boronic acid(cas: 768-35-4Name: (3-Fluorophenyl)boronic acid)
(3-Fluorophenyl)boronic acid(cas: 768-35-4) can be used to make novel liquid crystalline fluorobiphenylcyclohexenes and difluoroterphenyls by palladium-catalyzed cross-couplings also used in the synthesis of o-phenylphenols as potent leukotriene B4 receptor agonists.Name: (3-Fluorophenyl)boronic acid
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics