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Fluorescent sensor array for high-precision pH classification with machine learning-supported mobile devices.
Kim, H.; Lee, S.; Min, J. S.; Kim, E.; Choi, J.; Ko, J. G.*; Kim, E.*
Dyes Pigm. 2021, 193, 109492. DOI: 10.1016/j.dyepig.2021.109492
Benefits of Chemical Sugar Modifications Introduced by Click Chemistry for Glycoproteomic Analyses.
Calle, B.; Bineva-Todd, G.; Marchesi, A.; Flynn, H.; Ghirardello, M; Tastan, O. Y.; Roustan, C.; Choi, J.; Galan, M. C.; Schumann, B.*; Malaker, S. A.*
J. Am. Soc. Mass Spectrom. 2021, 32, 2366−2375. DOI:10.1021/jasms.1c00084
Optimization of Metabolic Oligosaccharide Engineering with Ac4GalNAlk and Ac4GlcNAlk by an Engineered Pyrophosphorylase.
Cioce, A; Bineva-Todd, G.; Agbay, A. J.; Choi, J.; Wood, T. M.; Debets, M. F.; Browne, W. M.; Douglas, H. L.; Roustan, C.; Tastan, O. Y.; Kjaer, S.; Bush, J. T.; Bertozzi, C. R.; Schumann, B.*
ACS Chem. Biol. 2021, ASAP. DOI:10.1021/acschembio.1c00034
Metabolic precision labeling enables selective probing of O-linked N-acetylgalactosamine glycosylation.
Debets, M. F.; Tastan, O. Y.; Wisnovsky, S. P.; Malaker, S. A.; Angelis, N.; Moeckl, L. K. R.; Choi, J.; Flynn, H.; Wagner, L. J. S.; Bineva-Todd, G.; Antonopoulos, A.; Cioce, A.; Browne, W. M.; Li, Z.; Briggs, D. C.; Douglas, H. L.; Hess, G. T.; Agbay, A. J.; Roustan, C.; Kjaer, S.; Haslam, S. M.; Snijders, A. P.; Bassik, M. C.; Moerner, W. E.; Li, V. S. W.; Bertozzi, C. R.; Schumann, B.*
Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 25293−25301. DOI: 10.1073/pnas.2007297117
Bump-and-Hole Engineering Identifies Specific Substrates of Glycosyltransferases in Living Cells.
Schumann, B.*; Malaker, S. A.; Wisnovsky, S. P.; Debets, M. F.; Agbay, A. J.; Fernandez, D.; Wagner, L. J. S.; Lin, L.; Li, Z.; Choi, J.; Fox, D. M.; Peh, J.; Gray, M. A.; Pedram, K.; Kohler, J. J.; Mrksich, M.; Bertozzi C. R.*
Mol. Cell 2020, 78, 824−883. DOI: 10.1016/j.molcel.2020.03.030
Phase Behavior of Disk Coil Block Copolymers under Cylindrical Confinement: Curvature Induced Structural Frustrations.
Ha, M. Y.†; Ryu, J. H.†; Cho, E. N.; Choi, J.; Kim, Y.*; Lee, W. B.* († contributed equally)
Phys. Rev. E 2019, 100, 052502. DOI: 10.1103/PhysRevE.100.052502
Engineering Orthogonal Polypeptide GalNAc-Transferase and UDP-Sugar Pairs.
Choi, J.†; Wagner, L. J. S.†; Timmermans, S. B. P. E.; Malaker, S. A.; Schumann, B.; Gray, M. A.; Debets, M. F.; Takashima, M.;Gehring, J.; Bertozzi, C. R.* († contributed equally)
J. Am. Chem. Soc. 2019, 141, 13442−13453. DOI: 10.1021/jacs.9b04695
Theoretical Study on the Toxicity of ‘Novichok’ Agent Candidates.
Jeong, K.*; Choi, J.
R. Soc. Open Sci. 2019, 6, 190414. DOI: 10.1098/rsos.190414
Transition Metal-Catalyzed Alkyl–Alkyl Bond Formation: Another Dimension in Cross-Coupling Chemistry.
Choi, J.; Fu, G. C.*
Science 2017, 356, eaaf7230. DOI: 10.1126/science.aaf7230
A General, Modular Method for the Catalytic Asymmetric Synthesis of Alkylboronate Esters.
Schmidt, J.; Choi, J.; Liu, A. T.; Slusarczyk, M.; Fu, G. C.*
Science 2016, 354, 1265−1269. DOI: 10.1126/science.aai8611
Enantioselective Decarboxylative Arylation of α-Amino Acids via the Merger of Photoredox and Nickel Catalysis.
Zuo, Z.†; Cong, H.†; Li, W; Choi, J.; Fu, G. C.*; MacMillan, D. W. C.* († contributed equally)
J. Am. Chem. Soc. 2016, 138, 1832−1835. DOI: 10.1021/jacs.5b13211
Stereoconvergent Arylations and Alkenylations of Unactivated Alkyl Electrophiles: The Catalytic
Enantioselective Synthesis of Secondary Sulfonamides and Sulfones.
Choi, J.; Martín-Gago, P.; Fu, G. C.*
J. Am. Chem. Soc. 2014, 136, 12161−12165 (spotlighted in JACS). DOI: 10.1021/ja506885s
A Versatile Approach to Ullmann C−N Couplings at RoomTemperature: New Families of Nucleophiles and
Electrophiles for Photoinduced, Copper-Catalyzed Processes.
Ziegler, D. T.; Choi, J.; Muñoz-Molina, J. M.; Bissember, A. C.; Peters, J. C.*; Fu, G. C.*
J. Am. Chem. Soc. 2013, 135, 13107−13112. DOI: 10.1021/ja4060806
Catalytic Asymmetric Synthesis of Secondary Nitriles via Stereoconvergent Negishi Arylations and
Alkenylations of Racemic α-Bromonitriles.
Choi, J.; Fu, G. C.*
J. Am. Chem. Soc. 2012, 134, 9102−9105. DOI: 10.1021/ja303442q
