
@article {163,
	title = {Boronic acid-promoted site-selective Fischer esterifications of sugar alcohols},
	journal = {Green Chemistry},
	volume = {21},
	year = {2019},
	month = {2019},
	pages = { 5363{\textendash}5367 },
	isbn = {1463-9262},
	url = {http://dx.doi.org/10.1039/C9GC00901A},
	author = {Manhas, Sanjay and Lin, Yu Chen and Wang, Grace and Kyne, Luke T. and Taylor, Mark S.}
}
@article {147,
	title = {Dehydrative glycosidations of 2-deoxysugar derivatives catalyzed by an arylboronic ester},
	journal = {Carbohydrate Research},
	volume = {470},
	year = {2018},
	month = {2018/12/01/},
	pages = {42 - 49},
	abstract = {<p>An N-methylpyridinium-4-boronic ester acts as a catalyst for dehydrative glycosidations of 2-deoxy sugar-derived hemiacetals. The catalytic protocol is tolerant of functionalized acceptors, including alcohols bearing isopropylidene ketal, tert-butyl carbamate or benzyl carbamate groups. The results demonstrate that organoboron-catalyzed substitution reactions of alcohols, which have previously been conducted on π-activated (benzylic, allylic or propargylic) substrates, can also be used to achieve C{\textendash}O bond formation from carbohydrate-derived hemiacetals.</p>},
	keywords = {2-Deoxyglycoside, Boronic acid, Catalysis, Glycosidation},
	isbn = {0008-6215},
	url = {http://www.sciencedirect.com/science/article/pii/S0008621518304579},
	author = {Manhas, Sanjay and Taylor, Mark S.}
}
@article {139,
	title = {Boronic acids as phase-transfer reagents for Fischer glycosidations in low-polarity solvents},
	journal = {The Journal of Organic Chemistry},
	volume = {82},
	year = {2017},
	month = {10/2017},
	pages = {11406{\textendash}11417},
	type = {Article},
	doi = {http://dx.doi.org/10.1021/acs.joc.7b01880},
	author = {Manhas, Sanjay and Taylor, Mark S.*}
}
