J
Jesse B. Kidd
Researcher at University of Wisconsin-Madison
Publications - 6
Citations - 350
Jesse B. Kidd is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Enantioselective synthesis & Cycloaddition. The author has an hindex of 3, co-authored 6 publications receiving 152 citations. Previous affiliations of Jesse B. Kidd include Wilmington University & University of North Carolina at Wilmington.
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Journal ArticleDOI
Enantioselective Excited-State Photoreactions Controlled by a Chiral Hydrogen-Bonding Iridium Sensitizer
TL;DR: An exceptionally effective chiral photocatalyst that recruits prochiral quinolones using a series of hydrogen-bonding and π-π interactions and leads to efficient Dexter energy transfer and effective stereoinduction.
Journal ArticleDOI
Chiral Photocatalyst Structures in Asymmetric Photochemical Synthesis.
TL;DR: A review of the chiral catalyst structures for solution-phase asymmetric photochemistry can be found in this paper, including chiral organic sensitizers, inorganic chromophores, and soluble macromolecules.
Journal ArticleDOI
Enantioselective Intermolecular Excited-State Photoreactions Using a Chiral Ir Triplet Sensitizer: Separating Association from Energy Transfer in Asymmetric Photocatalysis.
Jian Zheng,Wesley B. Swords,Wesley B. Swords,Hoimin Jung,Kazimer L. Skubi,Jesse B. Kidd,Gerald J. Meyer,Mu-Hyun Baik,Tehshik P. Yoon +8 more
TL;DR: A highly enantioselective intermo-lecular [2+2] cycloaddition of 3-alkoxyquinolones catalyzed by a chiral hydrogen-bonding iridium photosensitizer suggests that a broader range of alternate design strategies for asymmetric photocatalysis might be possi-ble.
Journal ArticleDOI
Construction of Complex Cyclobutane Building Blocks by Photosensitized [2 + 2] Cycloaddition of Vinyl Boronate Esters.
Spencer O. Scholz,Jesse B. Kidd,Luca Capaldo,Luca Capaldo,Niecia E. Flikweert,Rowan M. Littlefield,Tehshik P. Yoon +6 more
TL;DR: In this paper, a photosensitized [2 + 2] cycloaddition with vinyl boronate esters is presented, which allows straightforward access to complex, densely functionalized cyclobutane scaffolds.
Journal ArticleDOI
Synthesis of β-substituted tryptamines by regioselective ring opening of aziridines.
TL;DR: 4-Nitrobenzyl carbamate (PNZ)-protected aziridines undergo regioselective ring opening to produce β-substituted tryptamines for a series of indoles, which can be further manipulated by PNZ removal under mild conditions.