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Boronic acids are often used in metal-catalyzed cross-coupling for C-C, C-N bond formation, and C-H functionalization. The widely utilized Suzuki-Miyaura coupling allows for the coupling of boronic acids with carbon halides and surrogates. Other known chemistry may includes 1,4-addition to activated alkenes, 1,2-addition to carbonyls and imines, addition to anhydrides, 1,4-addition to a,ß-unsaturated ketones(4), and 1,4-addition to esters and amides.
Green, I. R.; et al. 2-Arylnaphthoquinone analogues: potential anti-TB and pro-apoptotic agents. Journal name. 2011, 192-212.
Tomohiro Yasukawa et. al.Copper-catalyzed, aerobic oxidative cross-coupling of alkynes with arylboronic acids: remarkable selectivity in 2,6-lutidine media.. Organic & Biomolecular Chemistry. 2011, 9(18), 6208-6210.
Gefahrenhinweise (EU): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.