1414852-54-2Relevant academic research and scientific papers
Oxidative geminal functionalization of organoboron compounds
He, Zhi,Trinchera, Piera,Adachi, Shinya,St. Denis, Jeffrey D.,Yudin, Andrei K.
, p. 11092 - 11096 (2012)
Excellent tolerance: Stable acylboronates equipped with N-methyliminodiacetyl (MIDA) boryl groups ([B]) were prepared by using a sequence of oxidative manipulations at the boron-bound carbon center (green in scheme). Chemoselective transformations of these acylated organoboron building blocks yielded a range of multifunctionalized boron derivatives and supplied access to valuable borylated heterocycles (see scheme). Copyright
