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The Journal of Antibiotics|April 16, 2019
Targeting adenylate-forming enzymes with designed sulfonyladenosine inhibitorsMichaelyn C Lux, Lisa C Standke, Derek S Tan
Chemical Communications (Cambridge, England)|June 1, 2019
Synthesis of bicyclic ethers by a palladium-catalyzed oxidative cyclization-redox relay-π-allyl-Pd cyclization cascade reactionMichaelyn C Lux, Melissa L Boby, Joshua L Brooks, et al.
Science (New York, N.Y.)|August 13, 2021
Photomediated ring contraction of saturated heterocyclesJustin Jurczyk, Michaelyn C Lux, Donovon Adpressa, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 26, 2019
Structural basis for adenylation and thioester bond formation in the ubiquitin E1Zachary S Hann, Cheng Ji, Shaun K Olsen, et al.
Nature|August 14, 2024
Structural basis for transthiolation intermediates in the ubiquitin pathwayTomasz Kochańczyk, Zachary S Hann, Michaelyn C Lux, et al.
ACS Medicinal Chemistry Letters|October 15, 2025
General Synthesis and Properties of Bridged, Fused, and Spirocyclic Azacycles via Intramolecular C-H Bond AminationMichaelyn C Lux, Justin Jurczyk, Donovon Adpressa, et al.
Journal of the American Chemical Society|January 2, 2025
Interrogation of Enantioselectivity in the Photomediated Ring Contractions of Saturated HeterocyclesSojung F Kim, Jordan P Liles, Michaelyn C Lux, et al.
Organic Letters|May 23, 2024
Design and Semisynthesis of Biselectrophile-Functionalized Ubiquitin Probes To Investigate Transthioesterification ReactionsAvelyn Mae V Delos Reyes, Michaelyn C Lux, Zachary S Hann, et al.
Organic Letters|August 19, 2020
Synthesis of Bridged Bicyclic Amines by Intramolecular Amination of Remote C-H Bonds: Synergistic Activation by Light and HeatMichaelyn C Lux, Justin Jurczyk, Yu-Hong Lam, et al.
Journal of the American Chemical Society|February 12, 2024
Mechanistic Investigation, Wavelength-Dependent Reactivity, and Expanded Reactivity of N-Aryl Azacycle Photomediated Ring ContractionsSojung F Kim, Henrik Schwarz, Justin Jurczyk, et al.
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