《Intramolecular aryl-aryl coupling via C-F bond activation tolerant towards C-I functionality》 was published in Chemical Communications (Cambridge, United Kingdom) in 2020. These research results belong to Steiner, Ann-Kristin; Feofanov, Mikhail; Amsharov, Konstantin. Application of 1073353-89-5 The article mentions the following:
A transition-metal free activation of a particularly stable aromatic carbon-fluorine bond allowing intramol. aryl-aryl coupling which is orthogonal to carbon-iodine functionality was reported.2-(2-Fluoro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(cas: 1073353-89-5Application of 1073353-89-5) was used in this study.
2-(2-Fluoro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(cas: 1073353-89-5) belongs to esters. They are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market.Application of 1073353-89-5
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics