Publications
  • 32. Lin, R.; Dong, Y.; Liu, J.-X.;* Bai, L.; Gao, J.; Zhu, H.-L.; Zhao, J.* “Inclusion of methylviologen in symmetrical a,a′,d,d′-tetramethyl-cucurbit[6]uril”, RSC Advances, 2012, 2, 7754-7758.
  • 31. Qian, Y.; Zhang, L.; Ding, S.; Deng, X.; He, C.; Zheng, X.E.; Zhu, H-L; Zhao, J.* “A Fluorescent Probe for Rapid Detection of Hydrogen Sulfide in Blood Plasma and Brain Tissues in Mice”, Chem. Sci., 2012, 3(10), 2920-2923.
  • 30. Wang, Y.; He, J.; Chen, J.; Ren, L.; Jiang, B.*; Zhao, J.*. “Synthesis of Monodisperse, Hierarchically Mesoporous, Silica Microspheres Embedded with Magnetic Nanocrystallites”, ACS Appl. Mater. Interfaces, 2012, 2735-2742.
  • 29. Wei, W.; Zhu, T.; Wang, Y.; Yang, H.; Hao, Z.; Chen, P.*; Zhao, J.*. “Engineering a Gold-specific Regulon for Cell-based Visual Detection and Recovery of Gold”, Chem. Sci., 2012, 3, 1780-1784.
  • 28. Gao, W.; He, Z.; Qian, Y.; Zhao, J.*, Huang, Y.* “General Palladium-Catalyzed Aerobic Dehydrogenation to Generate Double Bonds” Chem. Sci., 2012, 3, 883.
  • 27. Qian, Y.; Karpus, J.; Kabil, O.; Zhu, H-L; Banerjee, R.; Zhao, J.; He, C.* “Selective Fluorescent Probes for Live-Cell Monitoring of Sulfide” Nature Commun., 2011, 2, 1506.
  • 26. Hou, Y.; Sun, J.; Pang, Z.; Lv, P.; Li, D.; Yan, L.; Zhang, H.; Zheng, E.*; Zhao, J.*; Zhu, H.-L.* “Synthesis and antitumor activity of 1,2,4-triazoles having 1,4-benzodioxan fragment as a novel class of potent methionine aminopeptidase type II inhibitors” Bioorg. Med. Chem., 2011, 5948-5954.
  • 25. Zhang, X.; Chen, D.; Zhao, M.; Zhao, J.*; Jia, A.;* Li, X. * “Synthesis of Isoquinolines via Rhodium(III)-Catalyzed Dehydrative C-C and C-N Coupling between Oximines and Alkynes” Adv. Synth. Catal. 2011, 719-723.
  • 24. Tao, C.;* Lv, A.; Zhao, N.; Yang, S.; Liu, X.; Zhou, J.; Liu, W.; Zhao, J.* “Ligand-Free Copper-Catalyzed Synthesis of Diaryl Thioethers from Aryl Halides and Thioacetamide” Synlett, 2011, 134-138.
  • 23. Qian, Y.; Ma, G.; Yang, Y.; Cheng, K.; Zheng, Q.-Z.; Mao, W.-J.; Shi, L.; Zhao, J.*; Zhu, H.-L.* “Synthesis, molecular modeling and biological evaluation of dithiocarbamates as novel antitubulin agents” Bioorg. Med. Chem., 2010, 18, 4310-4316.