Jiajia Dong - Publications

Affiliations: 
The Shanghai Institute of Organic Chemistry 
Area:
Organic Chemistry

27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Xin Y, Liu S, Liu Y, Qian Z, Liu H, Zhang B, Guo T, Thompson GJ, Stevens RC, Sharpless KB, Dong J, Shui W. Affinity selection of double-click triazole libraries for rapid discovery of allosteric modulators for GLP-1 receptor. Proceedings of the National Academy of Sciences of the United States of America. 120: e2220767120. PMID 36893261 DOI: 10.1073/pnas.2220767120  0.432
2021 Dong J, Sharpless KB, Gao B, Sun S, Chen J. Fluorosulfuryl Isocyanate Enabled SuFEx Ligation of Alcohols and Amines. Angewandte Chemie (International Ed. in English). PMID 34259368 DOI: 10.1002/anie.202105583  0.312
2021 Zhang J, Zhao X, Cappiello JR, Yang Y, Cheng Y, Liu G, Fang W, Luo Y, Zhang Y, Dong J, Zhang L, Sharpless KB. Identification of simple arylfluorosulfates as potent agents against resistant bacteria. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34244433 DOI: 10.1073/pnas.2103513118  0.361
2019 Giel MC, Smedley CJ, Mackie ERR, Guo T, Dong J, Soares da Costa TP, Moses JE. Metal-Free Synthesis of Functional 1-Substituted-1,2,3-Triazoles from Ethenesulfonyl Fluoride and Organic Azides. Angewandte Chemie (International Ed. in English). PMID 31709653 DOI: 10.1002/Anie.201912728  0.388
2019 Meng G, Guo T, Ma T, Zhang J, Shen Y, Sharpless KB, Dong J. Modular click chemistry libraries for functional screens using a diazotizing reagent. Nature. 574: 86-89. PMID 31578481 DOI: 10.1038/S41586-019-1589-1  0.545
2019 Barrow AS, Smedley CJ, Zheng Q, Li S, Dong J, Moses JE. The growing applications of SuFEx click chemistry. Chemical Society Reviews. PMID 31364998 DOI: 10.1039/C8Cs00960K  0.328
2019 Liu Z, Meng G, Guo T, Dong J, Wu P. Novel Approaches to Access Arylfluorosulfates and Sulfamoyl Fluorides Based on Sulfur (VI) Fluoride Exchange. Current Protocols in Chemical Biology. e64. PMID 30816629 DOI: 10.1002/Cpch.64  0.353
2018 Guo T, Meng G, Zhan X, Yang Q, Ma T, Xu L, Sharpless KB, Dong J. Back Cover: A New Portal to SuFEx Click Chemistry: A Stable Fluorosulfuryl Imidazolium Salt Emerging as an “F−SO2 +” Donor of Unprecedented Reactivity, Selectivity, and Scope (Angew. Chem. Int. Ed. 10/2018) Angewandte Chemie International Edition. 57: 2728-2728. DOI: 10.1002/Anie.201801651  0.478
2017 Guo T, Meng G, Zhan X, Yang Q, Ma T, Xu L, Sharpless KB, Dong J. A New Portal to SuFEx Click Chemistry: a Stable Fluorosulfuryl Imidazolium Salt Emerging as an "F-SO2+" Donor of Unprecedented Reactivity, Selectivity, and Scope. Angewandte Chemie (International Ed. in English). PMID 29276888 DOI: 10.1002/Anie.201712429  0.52
2017 Gao B, Zhang L, Zheng Q, Zhou F, Klivansky LM, Lu J, Liu Y, Dong J, Wu P, Sharpless KB. Bifluoride-catalysed sulfur(VI) fluoride exchange reaction for the synthesis of polysulfates and polysulfonates. Nature Chemistry. 9: 1083-1088. PMID 29064495 DOI: 10.1038/Nchem.2796  0.512
2016 Zheng Q, Dong J, Sharpless KB. Ethenesulfonyl Fluoride (ESF): An On-Water Procedure for the Kilogram-Scale Preparation. The Journal of Organic Chemistry. PMID 27764941 DOI: 10.1021/Acs.Joc.6B01423  0.484
2016 Chen W, Dong J, Plate L, Mortenson DE, Brighty GJ, Li S, Liu Y, Galmozzi A, Lee PS, Hulce JJ, Cravatt BF, Saez E, Powers ET, Wilson IA, Sharpless KB, et al. Arylfluorosulfates Inactivate Intracellular Lipid Binding Protein(s) through Chemoselective SuFEx Reaction with a Binding-site Tyr Residue. Journal of the American Chemical Society. PMID 27191344 DOI: 10.1021/Jacs.6B02960  0.477
2015 Chen W, Dong J, Li S, Liu Y, Wang Y, Yoon L, Wu P, Sharpless KB, Kelly JW. Synthesis of Sulfotyrosine-Containing Peptides by Incorporating Fluorosulfated Tyrosine Using an Fmoc-Based Solid-Phase Strategy. Angewandte Chemie (International Ed. in English). PMID 26696445 DOI: 10.1002/Anie.201509016  0.418
2015 Baranczak A, Liu Y, Connelly S, Du WG, Greiner ER, Genereux JC, Wiseman RL, Eisele YS, Bradbury NC, Dong J, Noodleman L, Sharpless KB, Wilson IA, Encalada SE, Kelly JW. A Fluorogenic Aryl Fluorosulfate for Intraorganellar Transthyretin Imaging in Living Cells and in Caenorhabditis elegans. Journal of the American Chemical Society. 137: 7404-14. PMID 26051248 DOI: 10.1021/Jacs.5B03042  0.447
2015 Liang Q, Xing P, Huang Z, Dong J, Sharpless KB, Li X, Jiang B. Palladium-catalyzed, ligand-free Suzuki reaction in water using aryl fluorosulfates. Organic Letters. 17: 1942-5. PMID 25856416 DOI: 10.1021/Acs.Orglett.5B00654  0.505
2014 Dong J, Krasnova L, Finn MG, Sharpless KB. Sulfur(VI) fluoride exchange (SuFEx): another good reaction for click chemistry. Angewandte Chemie (International Ed. in English). 53: 9430-48. PMID 25112519 DOI: 10.1002/Anie.201309399  0.501
2014 Dong J, Sharpless KB, Kwisnek L, Oakdale JS, Fokin VV. SuFEx-based synthesis of polysulfates. Angewandte Chemie (International Ed. in English). 53: 9466-70. PMID 25100330 DOI: 10.1002/Anie.201403758  0.492
2014 Dong J, Krasnova L, Finn MG, Sharpless KB. ChemInform Abstract: Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry Cheminform. 45: no-no. DOI: 10.1002/chin.201447274  0.486
2014 Dong J, Krasnova L, Finn MG, Sharpless KB. Cover Picture: Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry (Angew. Chem. Int. Ed. 36/2014) Angewandte Chemie International Edition. 53: 9391-9391. DOI: 10.1002/Anie.201401157  0.53
2014 Dong J, Krasnova L, Finn MG, Sharpless KB. Titelbild: Schwefel(VI)-fluorid-Austausch (SuFEx): Eine weitere gute Anwendung für die Click-Chemie (Angew. Chem. 36/2014) Angewandte Chemie. 126: 9545-9545. DOI: 10.1002/Ange.201401157  0.462
2014 Dong J, Krasnova L, Finn MG, Sharpless KB. Schwefel(VI)-fluorid-Austausch (SuFEx): Eine weitere gute Anwendung für die Click-Chemie Angewandte Chemie. 126: 9584-9603. DOI: 10.1002/Ange.201309399  0.458
2013 Grimster NP, Connelly S, Baranczak A, Dong J, Krasnova LB, Sharpless KB, Powers ET, Wilson IA, Kelly JW. Aromatic sulfonyl fluorides covalently kinetically stabilize transthyretin to prevent amyloidogenesis while affording a fluorescent conjugate. Journal of the American Chemical Society. 135: 5656-68. PMID 23350654 DOI: 10.1021/Ja311729D  0.511
2011 Xu B, Feng Y, Cheng H, Song Y, Lv B, Wu Y, Wang C, Li S, Xu M, Du J, Peng K, Dong J, Zhang W, Zhang T, Zhu L, et al. C-aryl glucosides substituted at the 4'-position as potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the treatment of type 2 diabetes. Bioorganic & Medicinal Chemistry Letters. 21: 4465-70. PMID 21737266 DOI: 10.1016/J.Bmcl.2011.06.032  0.302
2011 Gastaminza P, Pitram SM, Dreux M, Krasnova LB, Whitten-Bauer C, Dong J, Chung J, Fokin VV, Sharpless KB, Chisari FV. Antiviral stilbene 1,2-diamines prevent initiation of hepatitis C virus RNA replication at the outset of infection. Journal of Virology. 85: 5513-23. PMID 21430055 DOI: 10.1128/Jvi.02116-10  0.407
2010 Xu B, Feng Y, Lv B, Xu G, Zhang L, Du J, Peng K, Xu M, Dong J, Zhang W, Zhang T, Zhu L, Ding H, Sheng Z, Welihinda A, et al. ortho-Substituted C-aryl glucosides as highly potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors. Bioorganic & Medicinal Chemistry. 18: 4422-32. PMID 20576578 DOI: 10.1016/J.Bmc.2010.04.088  0.31
2009 Jiang B, Zhao X, Dong J, Wang W. Catalytic Asymmetric Oxidation of Heteroaromatic Sulfides with tert-Butyl Hydroperoxide Catalyzed by a Titanium Complex with a New Chiral 1,2-Diphenylethane-1,2-diol Ligand European Journal of Organic Chemistry. 2009: 987-991. DOI: 10.1002/Ejoc.200801139  0.32
2008 Jiang B, Dong J, Jin Y, Du X, Xu M. The First Proline-Catalyzed Friedlander Annulation: Regioselective Synthesis of 2-Substituted Quinoline Derivatives European Journal of Organic Chemistry. 2008: 2693-2696. DOI: 10.1002/Ejoc.200800121  0.362
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