Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
2002 | A convenient chemoenzymatic synthesis of (4aS,5S)-(+)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one | Lo, L.-C.; Shie, J.-J.; Chou, T.-C.; LEE-CHIANG LO | Journal of Organic Chemistry | 7 | 7 | |
2002 | A Novel Photochromic System of 4,5-Dialkenylthiophenes Constructed by the Samarium Diiodide Promoted Coupling Reactions of Thiophene-2-carboxylate with Aryl Ketones | Shie, J.-J.; Yang, S.-M.; Chen, C.-T.; Fang, J.-M.; CHAO-TSEN CHEN ; JIM-MIN FANG | Organic Letters | 11 | 8 | |
2011 | A practical synthesis of zanamivir phosphonate congeners with potent anti-influenza activity | Shie, J.-J.; Fang, J.-M.; Lai, P.-T.; Wen, W.-H.; Wang, S.-Y.; Cheng, Y.-S.E.; Tsai, K.-C.; Yang, A.-S.; Wong, C.-H.; JIM-MIN FANG ; Pan, Tzu-Ming | Journal of the American Chemical Society | 72 | 70 | |
2014 | An azido-BODIPY probe for glycosylation: Initiation of strong fluorescence upon triazole formation | Shie, J.-J.; Liu, Y.-C.; Lee, Y.-M.; Lim, C.; Fang, J.-M.; Wong, C.-H.; JIM-MIN FANG | Journal of the American Chemical Society | 78 | 78 | |
2017 | A cell-permeable and triazole-forming fluorescent probe for glycoconjugate imaging in live cells | Shie, J.-J.; Liu, Y.-C.; Hsiao, J.-C.; Fang, J.-M. ; Wong, C.-H. | Chemical Communications | 14 | 13 | |
2014 | Chemical constituents of Plectranthus amboinicus and the synthetic analogs possessing anti-inflammatory activity | Chen, Y.-S.; Yu, H.-M.; Shie, J.-J.; Cheng, T.-J.R.; Wu, C.-Y.; Fang, J.-M.; Wong, C.-H.; JIM-MIN FANG | Bioorganic and Medicinal Chemistry | 38 | 32 | |
2004 | Comparative study of TmI2, SmI2, and SmI 2/HMPA in the cross-coupling reactions of 2-acetylthiophene and thiophene-2-carboxylate with carbonyl compounds | Shie, J.-J.; Workman, P.S.; Evans, W.J.; Fang, J.-M.; JIM-MIN FANG | Tetrahedron Letters | 11 | 11 | |
2019 | Development of effective anti-influenza drugs: Congeners and conjugates- A review | Shie, J.-J.; Fang, J.-M.; JIM-MIN FANG | Journal of Biomedical Science | 48 | 51 | |
2014 | From neuraminidase inhibitors to conjugates: A step towards better anti-influenza drugs? | Cheng, C.-K.; Tsai, C.-H.; Shie, J.-J.; Fang, J.-M.; JIM-MIN FANG | Future Medicinal Chemistry | 27 | 25 | |
2008 | In vitro evaluation of neuraminidase inhibitors using the neuraminidase-dependent release assay of hemagglutinin-pseudotyped viruses | Su, C.-Y.; Wang, S.-Y.; Shie, J.-J.; Jeng, K.-S.; Temperton, N.J.; Fang, J.-M.; Wong, C.-H.; Cheng, Y.-S.E.; JIM-MIN FANG | Antiviral Research | 21 | 20 |  |
2005 | Inhibition of the Severe Acute Respiratory Syndrome 3CL Protease by Peptidomimetic \,]-Unsaturated Esters | Shie, J.-J.; Fang, J.-M.; Kuo, T.-H.; Kuo, C.-J.; Liang, P.-H.; Huang, H.-J.; Wu, Y.-T.; Jan, J.-T.; Cheng, Y.-S. E.; Wong, C.-H. | Bioorganic & Medicinal Chemistry | | | |
2005 | Inhibition of the severe acute respiratory syndrome 3CL protease by peptidomimetic α,β-unsaturated esters | Shie, J.-J.; Fang, J.-M.; Kuo, T.-H.; Kuo, C.-J.; Liang, P.-H.; Huang, H.-J.; Wu, Y.-T.; Jan, J.-T.; Cheng, Y.-S.E.; Wong, C.-H.; JIM-MIN FANG | Bioorganic and Medicinal Chemistry | 97 | 83 |  |
2007 | Microwave-assisted one-pot tandem reactions for direct conversion of primary alcohols and aldehydes to triazines and tetrazoles in aqueous media | Shie, J.-J.; Fang, J.-M.; JIM-MIN FANG | Journal of Organic Chemistry | 119 | 107 |  |
2014 | Phosphonate congeners of oseltamivir and zanamivir as effective anti-influenza drugs: Design, synthesis and biological activity | Shie, J.-J.; Fang, J.-M.; JIM-MIN FANG | Journal of the Chinese Chemical Society | 9 | 9 | |
2010 | Regioselective synthesis of di-C-glycosylflavones possessing anti-inflammation activities | Shie, J.-J.; Chen, C.-A.; Lin, C.-C.; Ku, A.F.; Cheng, T.-J.R.; Fang, J.-M.; Wong, C.-H.; JIM-MIN FANG | Organic and Biomolecular Chemistry | 46 | 45 | |
2007 | Structural basis of mercury- and zinc-conjugated complexes as SARS-CoV 3C-like protease inhibitors | Lee, C.-C.; Kuo, C.-J.; Hsu, M.-F.; Liang, P.-H.; Fang, J.-M.; Shie, J.-J.; Wang, A.H.-J.; JIM-MIN FANG | FEBS Letters | 42 | 35 |  |
2007 | Synthesis of tamiflu and its phosphonate congeners possessing potent anti-influenza activity | Shie, J.-J.; Fang, J.-M.; Wang, S.-Y.; Tsai, K.-C.; Cheng, Y.-S.E.; Yang, A.-S.; Hsiao, S.-C.; Su, C.-Y.; Wong, C.-H.; JIM-MIN FANG | Journal of the American Chemical Society | 203 | 193 |  |
2014 | Tamiphosphor monoesters as effective anti-influenza agents | Chen, C.-L.; Lin, T.-C.; Wang, S.-Y.; Shie, J.-J.; Tsai, K.-C.; Cheng, Y.-S.E.; Jan, J.-T.; Lin, C.-J.; Fang, J.-M.; Wong, C.-H.; CHUN-JUNG LIN ; JIM-MIN FANG | European Journal of Medicinal Chemistry | 22 | 22 | |
2017 | Utilizing an iron(III)-chelation masking strategy to prepare mono- and bis-functionalized aerobactin analogues for targeting pathogenic bacteria | Ho, Y.-H.; Ho, S.-Y.; Hsu, C.-C. ; Shie, J.-J.; Wang, T.-S.A. | Chemical Communications | 5 | 5 | |
2017 | Utilizing an iron(III)-chelation masking strategy to prepare mono- and bis-functionalized aerobactin analogues for targeting pathogenic bacteria | Ho, Y.-H.; Ho, S.-Y.; Hsu, C.-C.; Shie, J.-J.; Wang, T.-S.A. | Chemical Communications | 5 | 5 | |