The Journal of Organic Chemistry · 2020 · 12 citations · 50 references
Materials ScienceArylboronic AcidsChemical EngineeringCross-coupling ReactionEngineeringBoron NitrideAryl BromideOrganic ChemistryBoropheneSynthetic ChemistryChemistryHalogenationBis-boronic AcidBorylation Reaction
In this study, we developed a simple transition-metal-free borylation reaction of aryl bromides. Bis-boronic acid (BBA), was used, and the borylation reaction was performed using a simple procedure at a mild temperature. Under mild conditions, aryl bromides were converted to arylboronic acids directly without any deprotection steps and purified by conversion to trifluoroborate salts. The functional group tolerance was considerably high. The mechanism study suggested that this borylation reaction proceeds via a radical pathway.
50
Thermal, Catalytic, Regiospecific Functionalization of Alkanes
Huiyuan Chen, Sabine Schlecht, Thomas C. Semple et al. · Science · 2000 · 873 citations
Boronic acid building blocks: tools for self assembly
Ryuhei Nishiyabu, Yuji Kubo, Tony D. James et al. · Chemical Communications · 2010 · 490 citations
Supramolecular Assembly, Engineering, Molecular Self-assembly +16