
@article {166,
	title = {Site-selective redox isomerizations of furanosides using a combined arylboronic acid/photoredox catalyst system},
	journal = {Chemical Science},
	volume = {11},
	year = {2020},
	month = {2020},
	pages = {1531 - 1537},
	abstract = {<p>In the presence of an arylboronic acid and a hydrogen atom transfer mediator under photoredox conditions, furanoside derivatives undergo site-selective redox isomerizations to 2-keto-3-deoxyfuranosides. Experimental evidence and computational modeling suggest that the transformation takes place by abstraction of the hydrogen atom from the 2-position of the furanoside-derived arylboronic ester, followed by C3{\textendash}O bond cleavage via spin-center shift. This mechanism is reminiscent of the currently accepted pathway for the formation of 3'-ketodeoxynucleotides by ribonucleotide reductase enzymes.</p>},
	isbn = {2041-6520},
	url = {http://dx.doi.org/10.1039/C9SC05173B},
	author = {Dimakos, Victoria and Gorelik, Daniel and Su, Hsin Y. and Garrett, Graham E. and Hughes, Gregory and Shibayama, Hiromitsu and Taylor, Mark S.}
}
@article {155,
	title = {Chiral phosphine ligand libraries based on the Bull{\textendash}James three-component supramolecular assembly},
	journal = {Supramolecular Chemistry},
	volume = {31},
	year = {2019},
	month = {2019/01/06},
	pages = {190{\textendash}202},
	isbn = {1061-0278},
	doi = {https://doi.org/10.1080/10610278.2018.1564829},
	url = {https://doi.org/10.1080/10610278.2018.1564829},
	author = {Su, Hsin Y. and Gorelik, Daniel and Taylor, Mark S.}
}
@article {154,
	title = {Diarylborinic Acid-Catalyzed, Site-Selective Sulfation of Carbohydrate Derivatives},
	journal = {The Journal of Organic Chemistry},
	volume = {84},
	year = {2019},
	month = {2019/01/08},
	pages = {900{\textendash}908},
	isbn = {0022-3263},
	doi = {https://doi.org/10.1021/acs.joc.8b02792},
	url = {https://doi.org/10.1021/acs.joc.8b02792},
	author = {Gorelik, Daniel and Lin, Yu Chen and Briceno-Strocchia, Alvaro I. and Taylor, Mark S.}
}
