
@article {233,
	title = {Synergistic Organoboron/Palladium Catalysis for Regioselective N-Allylation of 2-Pyridones, 4-Pyridones, and Related Ambident Heterocycles},
	journal = {Synlett},
	year = {2023},
	month = {2023/11/15},
	abstract = {The use of a boronic acid co-catalyst along with a palladium complex enables efficient dehydrative couplings of allylic alcohols and tautomerizable heterocycles. The protocol has been applied to achieve N-allylations of 2-pyridones, 4-pyridones, 4-pyrimidinones, and their benzo-fused derivatives.},
	keywords = {Allylation, Boronic acids, heterocycles, palladium, regioselectivity},
	isbn = {0936-52141437-2096},
	url = {http://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0043-1763618},
	author = {Yatzoglou, Giorgos and Zambri, Matthew T. and Desai, Shrey P. and Taylor, Mark S.}
}
@article {106,
	title = {Applications of organoboron compounds in carbohydrate chemistry and glycobiology: analysis, separation, protection, and activation},
	volume = {381},
	year = {2013},
	month = {2013/11/15/},
	pages = {112 - 122},
	abstract = {<p>AbstractThe reversible covalent interactions between organoboron compounds and diols have been applied for many years in carbohydrate chemistry. They form the basis of efficient methods for the detection of carbohydrates, and applications in cellular imaging and glycoprotein analysis are beginning to emerge. The interactions are also of widespread utility in carbohydrate synthesis: depending upon the coordination geometry at boron, either protection or activation of a bound diol motif may be achieved. This review article uses recent examples to illustrate the breadth of applications of organoboron compounds in carbohydrate chemistry.</p>},
	keywords = {Boronic acids, Carbohydrates, Catalysis, Drug delivery, Fluorescence, Glycosylation},
	isbn = {0008-6215},
	url = {http://www.sciencedirect.com/science/article/pii/S0008621513003443},
	author = {McClary, Corey A. and Taylor, Mark S.}
}
