A novel synthesis of arylboronic esters by a reductive electrochemical coupling reaction between aromatic halides and pinacolborane (HBpin, pin pinacolate) has been carried out leading to arylboronic esters in moderate to good yields.
Organo-boron compoundsOrgano-boron compounds S 0040 New Electrosynthesis of Arylboronic Esters from Aromatic Halides and Pinacolborane. -The mild reductive electrochemical coupling reaction between aromatic halides and pinacolborane is described. The reaction can be applied to non-activated aryl chlorides as well as to hindered aryl halides. The yields of pinacol esters obtained by electrolysis are slightly better than those reported by a chemical Pd-catalyzed procedure. -(LAZA, C.; DUNACH, E.; Adv. Synth. Catal. 345 (2003) 5, 580-583; Lab. Chim. Bio-Org., Fac. Sci., Univ. Nice-Sophia-Antipolis, F-06108 Nice, Fr.; Eng.) -Bartels 34-158
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.