
@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 {158,
	title = {Site-Selective and Stereoselective C{\textendash}H Alkylations of Carbohydrates via Combined Diarylborinic Acid and Photoredox Catalysis},
	journal = {Journal of the American Chemical Society},
	volume = {141},
	year = {2019},
	month = {2019/03/22},
	pages = {5149{\textendash}5153},
	isbn = {0002-7863},
	url = {https://doi.org/10.1021/jacs.9b01531},
	author = {Dimakos, Victoria and Su, Hsin Y. and Garrett, Graham E. and Taylor, Mark S.}
}
@article {128,
	title = {P-Stereogenic β-Aminophosphines: Preparation and Applications in Enantioselective Organocatalysis},
	journal = {The Journal of Organic Chemistry},
	volume = {82},
	year = {2017},
	month = {2017/03/17},
	pages = {3173 - 3182},
	isbn = {0022-3263},
	doi = {http://dx.doi.org/10.1021/acs.joc.7b00199},
	url = {http://pubs.acs.org/articlesonrequest/AOR-RxbAquas9MyXGG3VsVVV},
	author = {Su, Hsin Y. and Taylor, Mark S.}
}
@article {89,
	title = {A versatile synthesis of chiral beta-aminophosphines},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {14},
	year = {2016},
	month = {2016},
	pages = {5665 - 5672},
	abstract = {<p>A method for the preparation of chiral [small beta]-aminophosphines having substituted P-aryl groups is described. Ring-opening of cyclic sulfamidates with metal diarylphosphinites yields [small beta]-aminophosphine oxides, which are then reduced to the corresponding phosphines. Effects of the diarylphosphinite countercation on the regioselectivity of the ring-opening reaction (P- versus O-alkylation) are discussed. This method enables the introduction of electron-deficient, electron-rich and sterically hindered diarylphosphino groups, as demonstrated by the synthesis of a series of novel, P-aryl-substituted [small beta]-aminophosphines derived from tert-leucinol, valinol and phenylglycinol. Access to these derivatives will create new opportunities for steric and electronic tuning of [small beta]-aminophosphine-derived chiral ligands and organocatalysts.</p>},
	isbn = {1477-0520},
	url = {http://dx.doi.org/10.1039/C5OB02439K},
	author = {Su, Hsin Y. and Song, Yixiong and Taylor, Mark S.}
}
