Nickel-catalyzed decarboxylative arylation of azoles with perfluoro- and nitrobenzoates was written by Crawford, Jennifer M.;Shelton, Kyle E.;Reeves, Emily K.;Sadarananda, Bryce K.;Kalyani, Dipannita. And the article was included in Organic Chemistry Frontiers in 2015.Recommanded Product: 225104-76-7 This article mentions the following:
This manuscript describes a Ni-catalyzed method for the direct arylation of azoles using benzoates. Perfluorophenyl and 2-nitrobenzoates participate in these reactions to afford the corresponding products, e.g., I, in modest to good yields. The efficiency of the arylations with perfluorobenzoates is highly dependent on both the degree and position of fluorine atoms in the benzoates. In the experiment, the researchers used many compounds, for example, 3-Chloro-2,6-difluorobenzoic acid (cas: 225104-76-7Recommanded Product: 225104-76-7).
3-Chloro-2,6-difluorobenzoic acid (cas: 225104-76-7) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Recommanded Product: 225104-76-7
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics