Jun Ohata

A puromycin-dependent activity-based sensing probe for histochemical staining of hydrogen peroxide in cells and animal tissues

Nature Protocols.

Correction to “An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine–Azide Bioconjugation Method”

Correction to “An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine–Azide Bioconjugation Method.” Journal of the American Chemical Society.

Phosphine-Mediated Three-Component Bioconjugation of Amino- and Azidosaccharides in Ionic Liquids

Ohata, J., Hall, Y., Uzoewulu, C., Nizam, Z., Ishizawa, S., & El-Shaffey, H. (2022, April 18). (Vol. 4). Vol. 4.

Site-specific DNA functionalization through the tetrazene-forming reaction in ionic liquids

Ishizawa, S., Tumurkhuu, M., Gross, E. J., & Ohata, J. (2022, January 20). CHEMICAL SCIENCE, Vol. 1.

An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine-Azide Bioconjugation Method

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 8.

Linear Hydrocarbon Chain Growth from a Molecular Diruthenium Carbide Platform

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 9.

Site-Specific DNA Functionalization through the Tetrazene-Forming Reaction in Ionic Liquids

Ishizawa, S., Tumurkhuu, M., Gross, E., & Ohata, J. (2021, September 13). (Vol. 9). Vol. 9.

Site-Specific DNA Functionalization through the Tetrazene-Forming Reaction in Ionic Liquids

Ishizawa, S., Tumurkhuu, M., Gross, E., & Ohata, J. (2021, September 13). (Vol. 9). Vol. 9.

An Activity-Based Methionine Bioconjugation Approach To Developing Proximity-Activated Imaging Reporters

ACS Central Science, 6(1), 32–40.

Activity-Based Sensing Methods for Monitoring the Reactive Carbon Species Carbon Monoxide and Formaldehyde in Living Systems

Accounts of Chemical Research.

An Activity-Based Methionine Bioconjugation Approach to Developing Proximity-Activated Imaging Reporters

Ohata, J., Krishnamoorthy, L., Gonzalez, M., Xiao, T., Iovan, D., Toste, F. D., … Chang, C. (2019, October 16). (Vol. 10). Vol. 10.

Metallvermittelte Funktionalisierung natürlicher Peptide und Proteine: Biokonjugation mit Übergangsmetallen

Angewandte Chemie, 131(19), 6238–6264.

Metal‐Mediated Functionalization of Natural Peptides and Proteins: Panning for Bioconjugation Gold

Angewandte Chemie International Edition, 58(19), 6176–6199.

Rapid nickel(ii)-promoted cysteine S-arylation with arylboronic acids

Chemical Communications.

A Naturally Encoded Dipeptide Handle for Bioorthogonal Chan-Lam Coupling

Angewandte Chemie International Edition, 57(15), 4015–4019.

A Three-Component Organometallic Tyrosine Bioconjugation

Angewandte Chemie International Edition, 57(11), 2827–2830.

Rhodium at the Chemistry-Biology Interface

Dalton Transactions.

A Hexa-rhodium Metallopeptide Catalyst for Site-Specific Functionalization of Natural Antibodies

Journal of the American Chemical Society, 139(36), 12617–12622.

Ascorbate as a pro-oxidant: mild N-terminal modification with vinylboronic acids

Chemical Communications, 53(10), 1622–1625.

Histidine-Directed Arylation/Alkenylation of Backbone N–H Bonds Mediated by Copper(II)

Journal of the American Chemical Society, 138(24), 7472–7475.

Convenient analysis of protein modification by chemical blotting with fluorogenic “click” reagents

Molecular BioSystems, 11(11), 2846–2849.

Luminogenic iridium azide complexes

Chemical Communications, 51(82), 15192–15195.

Potent and selective inhibition of SH3 domains with dirhodium metalloinhibitors

Chemical Science, 6(8), 4778–4783.

A Diruthenium μ-Carbido Complex That Shows Singlet-Carbene-like Reactivity

Journal of the American Chemical Society, 136(45), 15889–15892.