Redox Chemistry of a Hydroxyphenyl-Substituted Borane

Chemical reduction of a hydroxyphenyl-substituted borane triggers a sequential electron-and intramolecular hydrogen-atom-transfer process to afford a hydridoborate phenoxide dianion. On the other hand, hydrogen-atom abstraction of the borane leads to the isolation of a neutral borylated phenoxyl radical, which can be transformed to the corresponding benzoquinone borataalkene derivative by reduction with cobaltocene.