
@article {167,
	title = {Borinic Acid-Catalyzed Regioselective Ring-Opening of 3,4- and 2,3-Epoxy Alcohols with Halides},
	journal = {Advanced Synthesis \& Catalysis},
	volume = {362},
	year = {2020},
	month = {2020/01/23},
	pages = {398 - 403},
	abstract = {<p>Abstract Methods for the regioselective ring-opening of 3,4-epoxy alcohols and 2,3-epoxy alcohols with halide nucleophiles, using a diarylborinic acid catalyst, are disclosed. Ring-opening occurs at the position proximal to the OH group, an effect ascribed to a catalytic tethering mechanism whereby coordination to the substrate OH group positions the diarylborinic acid to deliver a coordinated halide nucleophile. These methods provide access to halohydrin substitution patterns that were not previously accessible through catalytic epoxide ring-opening reactions.</p>},
	keywords = {boron, halides, homogeneous catalysis, regioselectivity.},
	isbn = {1615-4150},
	url = {https://doi.org/10.1002/adsc.201901268},
	author = {Wang, Grace and Taylor, Mark S.}
}
@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 {146,
	title = {Borinic Acid-Catalyzed, Regioselective Ring Opening of 3,4-Epoxy Alcohols},
	journal = {Organic Letters},
	volume = {20},
	year = {2018},
	month = {2018/08/27},
	pages = {5375{\textendash}5379},
	isbn = {1523-7060},
	url = {https://doi.org/10.1021/acs.orglett.8b02295},
	author = {Wang, Grace and Garrett, Graham E. and Taylor, Mark S.}
}
