Research outputs
2026
Iridium-Catalyzed Stereoselective α-Alkylation of α-Hydroxy Ketones with Minimally Polarized Alkenes
Wang, Y., Hong, F., Robertson, C. M., Mudd, R. J., & Bower, J. F. (2026). Iridium-Catalyzed Stereoselective α-Alkylation of α-Hydroxy Ketones with Minimally Polarized Alkenes. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 148(4), 3911-3917. doi:10.1021/jacs.5c19724
2025
<i>N</i> ‐Boc‐ <i>O</i> ‐tosylhydroxylamine
Lattanzi, A., Adams, R. J., Mudd, R. J., & Bower, J. F. (2025). <i>N</i> ‐Boc‐ <i>O</i> ‐tosylhydroxylamine. In Unknown Book (pp. 1-6). Wiley. doi:10.1002/047084289x.rn01753.pub2
The Discovery and Development of an Iridium-Catalyzed N→C Alkyl Transfer Reaction
Boddie, E. C., Cooper, P., Hammarback, L. A., Mudd, R. J., Feron, L. J., & Bower, J. F. (2025). The Discovery and Development of an Iridium-Catalyzed N→C Alkyl Transfer Reaction. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 64(40). doi:10.1002/anie.202509193
The Discovery and Development of an Iridium‐Catalyzed N→C Alkyl Transfer Reaction
Boddie, E. C., Cooper, P., Hammarback, L. A., Mudd, R. J., Feron, L. J., & Bower, J. F. (2025). The Discovery and Development of an Iridium‐Catalyzed N→C Alkyl Transfer Reaction. Angewandte Chemie, 137(40). doi:10.1002/ange.202509193
Benzamide-Directed Hydroarylative Cross-Couplings Using Minimally Activated Alkenes: Enantioselective Synthesis of Tertiary and Quaternary Stereocenters.
Aldhous, T. P., Chung, R., Hassan, A., Dalling, A. G., Cooper, P., Grélaud, S., . . . Bower, J. (2025). Benzamide-Directed Hydroarylative Cross-Couplings Using Minimally Activated Alkenes: Enantioselective Synthesis of Tertiary and Quaternary Stereocenters.. Angewandte Chemie (International ed. in English), e202502569. doi:10.1002/anie.202502569
Benzamide‐Directed Hydroarylative Cross‐Couplings Using Minimally Activated Alkenes: Enantioselective Synthesis of Tertiary and Quaternary Stereocenters
Aldhous, T. P., Chung, R., Hassan, A., Dalling, A. G., Cooper, P., Grélaud, S., . . . Bower, J. F. (2025). Benzamide‐Directed Hydroarylative Cross‐Couplings Using Minimally Activated Alkenes: Enantioselective Synthesis of Tertiary and Quaternary Stereocenters. Angewandte Chemie, 137(22). doi:10.1002/ange.202502569
2024
Directing Hydrogen Isotope Exchange with Aryl Carboxylic Acids
Mudd, R. J., Reid, M., Paterson, L. C., Atzrodt, J., Derdau, V., & Ker, W. J. (2024). Directing Hydrogen Isotope Exchange with Aryl Carboxylic Acids. SYNLETT, 35(19), 2201-2206. doi:10.1055/a-2239-6965
2018
Iridium-Catalyzed Csp<SUP>3</SUP>-H Activation for Mild and Selective Hydrogen Isotope Exchange
Kerr, W. J., Mudd, R. J., Reid, M., Atzrodt, J., & Derdau, V. (2018). Iridium-Catalyzed Csp<SUP>3</SUP>-H Activation for Mild and Selective Hydrogen Isotope Exchange. ACS CATALYSIS, 8(11), 10895-10900. doi:10.1021/acscatal.8b03565
2017
Deconstructing the Catalytic, <i>Vicinal</i> Difluorination of Alkenes: HF-Free Synthesis and Structural Study of <i>p</i>-TolIF<sub>2</sub>
Sarie, J. C., Thiehoff, C., Mudd, R. J., Daniliuc, C. G., Kehr, G., & Gilmour, R. (2017). Deconstructing the Catalytic, <i>Vicinal</i> Difluorination of Alkenes: HF-Free Synthesis and Structural Study of <i>p</i>-TolIF<sub>2</sub>. JOURNAL OF ORGANIC CHEMISTRY, 82(22), 11792-11798. doi:10.1021/acs.joc.7b01671
2016
Hydrogen isotope exchange with highly active iridium(I) NHC/phosphine complexes: a comparative counterion study
Kerr, W. J., Mudd, R. J., Owens, P. K., Reid, M., Brown, J. A., & Campos, S. (2016). Hydrogen isotope exchange with highly active iridium(I) NHC/phosphine complexes: a comparative counterion study. JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 59(14), 601-603. doi:10.1002/jlcr.3427
Iridium(I) N-Heterocyclic Carbene (NHC)/Phosphine Catalysts for Mild and Chemoselective Hydrogenation Processes
Kerr, W. J., Mudd, R. J., & Brown, J. A. (2016). Iridium(I) N-Heterocyclic Carbene (NHC)/Phosphine Catalysts for Mild and Chemoselective Hydrogenation Processes. CHEMISTRY-A EUROPEAN JOURNAL, 22(14), 4738-4742. doi:10.1002/chem.201504825
Abstracts of the 24th international isotope society (UK group) symposium: synthesis and applications of labelled compounds 2015.
Aigbirhio, F. I., Allwein, S., Anwar, A., Atzrodt, J., Audisio, D., Badman, G., . . . Xiao, J. (2016). Abstracts of the 24th international isotope society (UK group) symposium: synthesis and applications of labelled compounds 2015.. Journal of labelled compounds & radiopharmaceuticals, 59(4), 175-186. doi:10.1002/jlcr.3377
2014
Iridium(I)-Catalyzed Regioselective C-H Activation and Hydrogen-Isotope Exchange of Non-aromatic Unsaturated Functionality
Kerr, W. J., Mudd, R. J., Paterson, L. C., & Brown, J. A. (2014). Iridium(I)-Catalyzed Regioselective C-H Activation and Hydrogen-Isotope Exchange of Non-aromatic Unsaturated Functionality. CHEMISTRY-A EUROPEAN JOURNAL, 20(45), 14604-14607. doi:10.1002/chem.201405114
2012
Gold(I)-Catalyzed Addition of Thiols and Thioacids to 3,3-Disubstituted Cyclopropenes
Mudd, R. J., Young, P. C., Jordan-Hore, J. A., Rosair, G. M., & Lee, A. -L. (2012). Gold(I)-Catalyzed Addition of Thiols and Thioacids to 3,3-Disubstituted Cyclopropenes. JOURNAL OF ORGANIC CHEMISTRY, 77(17), 7633-7639. doi:10.1021/jo300930c
Divergent Outcomes of Gold(I)-Catalyzed Indole Additions to 3,3-Disubstituted Cyclopropenes
Young, P. C., Hadfield, M. S., Arrowsmith, L., Macleod, K. M., Mudd, R. J., Jordan-Hore, J. A., & Lee, A. -L. (2012). Divergent Outcomes of Gold(I)-Catalyzed Indole Additions to 3,3-Disubstituted Cyclopropenes. ORGANIC LETTERS, 14(3), 898-901. doi:10.1021/ol203418u