1610366-45-4Relevant academic research and scientific papers
Metal-free halogenation of arylboronate with N-halosuccinimide
Kamei, Toshiyuki,Ishibashi, Aoi,Shimada, Toyoshi
, p. 4245 - 4247 (2014)
Efficient bromination and chlorination of aryl pinacol boronates were accomplished without the addition of metal reagent. The reaction proceeded efficiently with electron-rich arylboronates or heteroarylboronates in DMF or acetonitrile, to afford mono-, di-, or trihalogenated aryl pinacol boronates.
Metal-free halogenation of arylboronate with N-halosuccinimide
Kamei, Toshiyuki,Ishibashi, Aoi,Shimada, Toyoshi
, p. 4245 - 4247 (2014/07/22)
Efficient bromination and chlorination of aryl pinacol boronates were accomplished without the addition of metal reagent. The reaction proceeded efficiently with electron-rich arylboronates or heteroarylboronates in DMF or acetonitrile, to afford mono-, d
Base-promoted protodeboronation of 2,6-disubstituted arylboronic acids
Lozada, Jerome,Liu, Zhibo,Perrin, David M.
, p. 5365 - 5368 (2014/06/23)
Facile based promoted deboronation of electron-deficient arylboronate esters was observed for arylboronates containing two ortho electron-withdrawing group (EWG) substituents. Among 30 representative boronates, only the diortho-substituted species underwe
