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J., & Ohata, J. (2022, June 7). Site-specific DNA functionalization through the tetrazene-forming reaction in ionic liquids (vol 13, pg 1780, 2022). CHEMICAL SCIENCE, Vol. 13, pp. 6749–6751. https://doi.org/10.1039/d2sc90102a Uzoewulu, C. P., & Ohata, J. (2022, August 24). Translation of a Phosphine- and Azide-Based Reaction to Chemical Modification of Biomolecules in Ionic Liquid. SYNLETT, Vol. 7. https://doi.org/10.1055/a-1908-2066 Uzoewulu, C., & Ohata, J. (2022, July 11). Translation of a phosphine- and azide-based reaction to chemical modification of biomolecules in ionic liquid. https://doi.org/10.26434/chemrxiv-2022-k3rc1 El-Shaffey, H. M., Gross, E. J., Hall, Y. D., & Ohata, J. (2021). An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine-Azide Bioconjugation Method. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143(33), 12974–12979. https://doi.org/10.1021/jacs.1c06092 Ohata, J., Teramoto, A., Fujita, H., Takemoto, S., & Matsuzaka, H. (2021). Linear Hydrocarbon Chain Growth from a Molecular Diruthenium Carbide Platform. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143(39), 16105–16112. https://doi.org/10.1021/jacs.1c06586 Ishizawa, S., Tumurkhuu, M., Gross, E., & Ohata, J. (2021, September 13). Site-Specific DNA Functionalization through the Tetrazene-Forming Reaction in Ionic Liquids (Vol. 9). Vol. 9. https://doi.org/10.33774/chemrxiv-2021-zkz9w Ishizawa, S., Tumurkhuu, M., Gross, E., & Ohata, J. (2021, September 13). Site-Specific DNA Functionalization through the Tetrazene-Forming Reaction in Ionic Liquids (Vol. 9). Vol. 9. https://doi.org/10.26434/chemrxiv-2021-zkz9w Ohata, J., Krishnamoorthy, L., Gonzalez, M. A., Xiao, T., Iovan, D. A., Toste, F. D., … Chang, C. J. (2020). An Activity-Based Methionine Bioconjugation Approach To Developing Proximity-Activated Imaging Reporters. ACS Central Science, 6(1), 32–40. https://doi.org/10.1021/acscentsci.9b01038 Activity-Based Sensing Methods for Monitoring the Reactive Carbon Species Carbon Monoxide and Formaldehyde in Living Systems. (2019). Accounts of Chemical Research. https://doi.org/10.1021/acs.accounts.9b00386 Ohata, J., Krishnamoorthy, L., Gonzalez, M., Xiao, T., Iovan, D., Toste, F. D., … Chang, C. (2019, October 16). An Activity-Based Methionine Bioconjugation Approach to Developing Proximity-Activated Imaging Reporters (Vol. 10). Vol. 10. https://doi.org/10.26434/chemrxiv.9964256.v1 Ohata, J., Martin, S. C., & Ball, Z. T. (2019). Metallvermittelte Funktionalisierung natürlicher Peptide und Proteine: Biokonjugation mit Übergangsmetallen. Angewandte Chemie, 131(19), 6238–6264. https://doi.org/10.1002/ange.201807536 Ohata, J., Martin, S. C., & Ball, Z. T. (2019). Metal‐Mediated Functionalization of Natural Peptides and Proteins: Panning for Bioconjugation Gold. Angewandte Chemie International Edition, 58(19), 6176–6199. https://doi.org/10.1002/anie.201807536 Hanaya, K., Ohata, J., Miller, M. K., Mangubat-Medina, A. E., Swierczynski, M. J., Yang, D. C., … Ball, Z. T. (2019). Rapid nickel(ii)-promoted cysteine S-arylation with arylboronic acids. Chemical Communications. https://doi.org/10.1039/C9CC00159J Ohata, J., Zeng, Y., Segatori, L., & Ball, Z. T. (2018). A Naturally Encoded Dipeptide Handle for Bioorthogonal Chan-Lam Coupling. Angewandte Chemie International Edition, 57(15), 4015–4019. https://doi.org/10.1002/anie.201800828 Ohata, J., Miller, M. K., Mountain, C. M., Vohidov, F., & Ball, Z. T. (2018). A Three-Component Organometallic Tyrosine Bioconjugation. Angewandte Chemie International Edition, 57(11), 2827–2830. https://doi.org/10.1002/anie.201711868 Ohata, J., & Ball, Z. T. (2018). Rhodium at the Chemistry-Biology Interface. Dalton Transactions. https://doi.org/10.1039/c8dt03032d Ohata, J., & Ball, Z. T. (2017). A Hexa-rhodium Metallopeptide Catalyst for Site-Specific Functionalization of Natural Antibodies. Journal of the American Chemical Society, 139(36), 12617–12622. https://doi.org/10.1021/jacs.7b06428 Ohata, J., & Ball, Z. T. (2017). Ascorbate as a pro-oxidant: mild N-terminal modification with vinylboronic acids. Chemical Communications, 53(10), 1622–1625. https://doi.org/10.1039/c6cc09955f Ohata, J., Minus, M. B., Abernathy, M. E., & Ball, Z. T. (2016). Histidine-Directed Arylation/Alkenylation of Backbone N–H Bonds Mediated by Copper(II). Journal of the American Chemical Society, 138(24), 7472–7475. https://doi.org/10.1021/jacs.6b03390 Ohata, J., Vohidov, F., & Ball, Z. T. (2015). Convenient analysis of protein modification by chemical blotting with fluorogenic “click” reagents. Molecular BioSystems, 11(11), 2846–2849. https://doi.org/10.1039/c5mb00510h Ohata, J., Vohidov, F., Aliyan, A., Huang, K., Martí, A. A., & Ball, Z. T. (2015). Luminogenic iridium azide complexes. Chemical Communications, 51(82), 15192–15195. https://doi.org/10.1039/c5cc06099k Vohidov, F., Knudsen, S. E., Leonard, P. G., Ohata, J., Wheadon, M. J., Popp, B. V., … Ball, Z. T. (2015). Potent and selective inhibition of SH3 domains with dirhodium metalloinhibitors. Chemical Science, 6(8), 4778–4783. https://doi.org/10.1039/c5sc01602a Takemoto, S., Ohata, J., Umetani, K., Yamaguchi, M., & Matsuzaka, H. (2014). A Diruthenium μ-Carbido Complex That Shows Singlet-Carbene-like Reactivity. Journal of the American Chemical Society, 136(45), 15889–15892. https://doi.org/10.1021/ja509364d