
@article {165,
	title = {Copper-mediated anomeric O-arylation with organoboron reagents},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {17},
	year = {2019},
	month = {2019},
	pages = {5671 - 5674},
	abstract = {<p>Copper-mediated couplings of arylboroxines with glycosyl hemiacetals furnish O-aryl glycosides via Csp2{\textendash}O bond formation. The method enables the anomeric O-arylation of protected pyranose and furanose derivatives, and is tolerant of functionalized arylboroxine partners. Whereas mixtures of anomers are formed from glucopyranose, galactopyranose and arabinofuranose hemiacetals, the α-anomer is generated selectively from mannopyranose and mannofuranose-derived substrates.</p>},
	isbn = {1477-0520},
	url = {http://dx.doi.org/10.1039/C9OB01022J},
	author = {Dimakos, Victoria and Liu, Jacklyn J. W. and Ge, Zhenlu and Taylor, Mark S.}
}
