| Literature DB >> 27005399 |
Marc-André Légaré1, Étienne Rochette1, Julien Légaré Lavergne1, Nicolas Bouchard1, Frédéric-Georges Fontaine1.
Abstract
While the organotrifluoroborate group is commonly used as a leaving group in cross-coupling reactions, we now show that their high stability can be used to protect the Lewis acidic moieties of frustrated Lewis pair catalysts. Indeed, the air and moisture-stable trifluoro- and difluoroborate derivatives of bulky (tetramethylpiperidino)benzene are shown to be conveniently converted to their dihydroborane analogue which is known to activate small molecules. An efficient synthesis route to these stable and convenient precatalysts, their deprotection chemistry and their benchtop use for the dehydrogenative borylation of heteroarenes is presented.Entities:
Year: 2016 PMID: 27005399 DOI: 10.1039/c6cc01267a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222