I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
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.
Hazard Statements: H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P261-P280a-P305+P351+P338-P304+P340-P405-P501a
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.