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Browsing by Author Hung, S. -C.


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Issue DateTitleAuthor(s)RelationscopusWOSFulltext/Archive link
20062-Allyloxyphenyl Glycoside as a New and Stable Type of Glycosyl DonorsLee, J. -C.; Pan, G. -R.; Kulkarni, S. S.; Luo, S. -Y.; Liao, C. -C.; Hung, S. -C.Tetrahedron Lett. 47, 1621–1624
20122-Allylphenyl Glycosides as Glycosyl Donors for Sugar CouplingLuo, S. -Y.; Tripathi, A.; Zulueta, M. M. L.; Hung, S. -C.Carbohydrate Research 352, 197-201
2006A Concise Synthesis of Tetrahydroxy-LCB, -Galactosyl Ceramide, and 1,4-Dideoxy-1,4-imino-L-ribitol via D-Allosamines as Key Building BlocksLuo, S. -Y.; Kulkarni, S. S.; Chou, C. -H.; Liao, W. -M.; Hung, S. -C.J. Org. Chem. 71, 1226–1229
2002A Highly Diastereoselective Synthesis of (1R)-(+)-Camphor Based Chiral Allenes and their Asymmetric Hydroboration-Oxidation ReactionsHung, S. -C.; Wen, Y. -F.; Chang, J. -W.; Liao, C. -C.; Uang, B. -J.J. Org. Chem. 67, 1308–1313
2012Acyl and Silyl Group Effects in Reactivity-based One-pot Glycosylation: Synthesis of Embryonic Stem Cell Surface Carbohydrates Lc4 and IV2Fuc-Lc4Hsu, Y.; Lu, X. -A.; Zulueta, M. M. L.; Tsai, C. -M.; Lin, K. -I; Hung, S. -C.; Wong, C. -H.J. Am. Chem. Soc. 134, 4549-4552
2004Biologically Potent L-Hexoses and 6-Deoxy-L-hexoses: Their Syntheses and ApplicationsKulkarni, S. S.; Chi, F. -C.; Hung, S. -C.Journal of the Chinese Chemical Society 51, 1193–1200
2007Breakthrough in Carbohydrate SynthesisHung, S. -C.Newsletter NTHU 1(3), 6-7
2008Carbohydrates-Templated Asymmetric Diels-Alder Reactions of Masked ortho-Benzoquinones for the Synthesis of Chiral Bicyclo[2.2.2]oct-5-en-2-onesLuo, S. -Y.; Jang, Y. -J.; Liu, J. -Y.; Chu, C. -S.; Liao, C. -C.; Hung, S. -C.Angewandte Chemie-International Edition 47, 8082–8085
2008Characterization of Molecular Interactions between Eosinophil Cationic Protein and HeparinFan, T. -C.; Fang, S. -L.; Hwang, C. -S.; Hsu, C. -Y.; Lu, X. -A.; Hung, S. -C.; Lin, S. -C.; Chang, M. D. T.J. Biol. Chem. 283, 25468–25474
2005Cu(OTf)2 as an Efficient and Dual-Purpose Catalyst in the Regioselective Reductive Ring Opening of Benzylidene AcetalsShie, C. -R.; Tzeng, Z. -H.; Kulkarni, S. S.; Uang, B. -J.; Hsu, C. -Y.; Hung, S. -C.Angewandte Chemie-International Edition 44, 1665–1668
2003Cu(OTf)2-catalyzed Et3SiH-reductive Etherification of Various Carbonyl Compounds with Trimethylsilyl EthersYang, W. -C.; Lu, X. -A.; Kulkarni, S. S.; Hung, S. -C.Tetrahedron Lett. 44, 7837–7840
2011Desymmetrization of 2,4,5,6-Tetra-O-benzyl-D-myo-inositol for the Synthesis of MycothiolChung, C. -C.; Zulueta, M. M. L.; Padiyar, L. T.; Hung, S. -C.Org. Lett. 13, 5496–5499
2011Deuterium-Isotope Study on the Regioselective Ring Opening of Benzylidene AcetalsLee, I. -C.; Zulueta, M. M. L.; Shie, C. -R.; Arco, S. D.; Hung, S. -C.Org. Biomol. Chem. 9, 7655–7658
2013Development and Application of Flow ChemistryChen, Z. -G.; Hu, Y. -P.; Hung, S. -C.Instruments Today, 66-73
2012Divergent Synthesis of 48 Heparan Sulfate-Based Disaccharides and Probing the Specific Sugar–Fibroblast Growth Factor-1 InteractionHu, Y. -P.; Zhong, Y. -Q.; Chen, Z. -G.; Chen, C. -Y.; Shi, Z.; Zulueta, M. M. L.; Ku, C. -C.; Lee, P. -Y.; Wang, C. -C.; Hung, S. -C.J. Am. Chem. Soc. 134, 20722-20727
2000Efficient Synthesis of 1,2,3,4,6-Penta-O-acetyl-L-idopyranoseHung, S. -C.; Chen, C. -S.Journal of the Chinese Chemical Society 47, 1257–1262
2003Facile Cu(OTf)2-catalyzed Preparation of Per-O-acetylated Hexopyranoses with Stoichiometric Acetic Anhydride and Sequential One-pot Anomeric Substitution to Thioglycosides under Solvent-free ConditionsTai, C. -A.; Kulkarni, S. S.; Hung, S. -C.J. Org. Chem. 68, 8719–8722
2005Metal Trifluoromethanesulfonates as Versatile Catalysts in Carbohydrate SynthesisKulkarni, S. S.; Hung, S. -C.Lett. Org. Chem. 2, 670–677
2010Metal Trifluromethanesulfonate-Catalyzed Regioselective Acylation of myo-Inositol OrthoformatePadiyar, L. T.; Wen, Y. -S.; Hung, S. -C.Chem. Commun. 46, 5524-5526
2005Neighboring Group Participation of 9-Anthracenylmethyl Group in Glycosylation: Preparation of Unusual C-GlycosidesKulkarni, S. S.; Liu, Y. -H.; Hung, S. -C.J. Org. Chem. 70, 2808–2811
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