| Year |
Citation |
Score |
| 2022 |
Tseng KY, Tzeng ZH, Cheng TR, Liang PH, Hung SC. Design and Synthesis of 1-- and 6'--Modified Heparan Sulfate Trisaccharides as Human Endo-6--Sulfatase 1 Inhibitors. Frontiers in Chemistry. 10: 947475. PMID 35910734 DOI: 10.3389/fchem.2022.947475 |
0.632 |
|
| 2022 |
Weng WC, Liao HE, Huang SP, Tsai ST, Hsu HC, Liew CY, Gannedi V, Hung SC, Ni CK. Unusual free oligosaccharides in human bovine and caprine milk. Scientific Reports. 12: 10790. PMID 35750794 DOI: 10.1038/s41598-022-15140-7 |
0.722 |
|
| 2022 |
Uchimura K, Nishitsuji K, Chiu LT, Ohgita T, Saito H, Allain F, Gannedi V, Wong CH, Hung SC. Design and Synthesis of 6-O-Phosphorylated Heparan Sulfate Oligosaccharides to Inhibit Amyloid β Aggregation. Chembiochem : a European Journal of Chemical Biology. e202200191. PMID 35585797 DOI: 10.1002/cbic.202200191 |
0.709 |
|
| 2021 |
Gannedi V, Villuri BK, Reddy SN, Ku CC, Wong CH, Hung SC. Practical Remdesivir Synthesis through One-Pot Organocatalyzed Asymmetric ()-P-Phosphoramidation. The Journal of Organic Chemistry. PMID 33634692 DOI: 10.1021/acs.joc.0c02888 |
0.743 |
|
| 2021 |
Jan JT, Cheng TR, Juang YP, Ma HH, Wu YT, Yang WB, Cheng CW, Chen X, Chou TH, Shie JJ, Cheng WC, Chein RJ, Mao SS, Liang PH, Ma C, ... Hung SC, et al. Identification of existing pharmaceuticals and herbal medicines as inhibitors of SARS-CoV-2 infection. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33452205 DOI: 10.1073/pnas.2021579118 |
0.688 |
|
| 2020 |
Gopinathan P, Chiang NJ, Bandaru A, Sinha A, Huang WY, Hung SC, Shan YS, Lee GB. Exploring Circulating Tumor Cells in Cholangiocarcinoma Using a Novel Glycosaminoglycan Probe on a Microfluidic Platform. Advanced Healthcare Materials. e1901875. PMID 32329247 DOI: 10.1002/adhm.201901875 |
0.738 |
|
| 2020 |
Chiu LT, Sabbavarapu NM, Lin WC, Fan CY, Wu CC, Cheng TR, Wong CH, Hung SC. A Trisaccharide Sulfate and its Sulfonamide as Effective Substrate and Inhibitor of Human Endo-O-sulfatase-1. Journal of the American Chemical Society. PMID 32083852 DOI: 10.1021/Jacs.0C00005 |
0.558 |
|
| 2020 |
Lin TS, Hsieh CH, Kuo C, Juang YP, Hsieh YSY, Chiang H, Hung SC, Jiang CC, Liang PH. Sulfation pattern of chondroitin sulfate in human osteoarthritis cartilages reveals a lower level of chondroitin-4-sulfate. Carbohydrate Polymers. 229: 115496. PMID 31826425 DOI: 10.1016/j.carbpol.2019.115496 |
0.583 |
|
| 2019 |
Sakamoto K, Ozaki T, Ko YC, Tsai CF, Gong Y, Morozumi M, Ishikawa Y, Uchimura K, Nadanaka S, Kitagawa H, Zulueta MML, Bandaru A, Tamura JI, Hung SC, Kadomatsu K. Glycan sulfation patterns define autophagy flux at axon tip via PTPRσ-cortactin axis. Nature Chemical Biology. PMID 31061498 DOI: 10.1038/S41589-019-0274-X |
0.739 |
|
| 2019 |
Kulkarni SS, Wang CC, Sabbavarapu NM, Podilapu AR, Liao PH, Hung SC. Correction to "One-Pot" Protection, Glycosylation, and Protection-Glycosylation Strategies of Carbohydrates. Chemical Reviews. PMID 30653294 DOI: 10.1021/Acs.Chemrev.8B00774 |
0.717 |
|
| 2018 |
Hung SC, Yeh CJ, Ku CC, Lin WC, Fan CY, Zulueta M, Manabe Y, Fukase K, Li YK. Single-step Per-O-sulfonation and 1,6-Anhydro-bridge Formation of Sugar Oligomers for Fibroblast Growth Factor Interactions. Chembiochem : a European Journal of Chemical Biology. PMID 30239102 DOI: 10.1002/Cbic.201800464 |
0.316 |
|
| 2018 |
Kulkarni SS, Wang CC, Sabbavarapu NM, Podilapu AR, Liao PH, Hung SC. "One-Pot" Protection, Glycosylation, and Protection-Glycosylation Strategies of Carbohydrates. Chemical Reviews. PMID 29870239 DOI: 10.1021/Acs.Chemrev.8B00036 |
0.749 |
|
| 2017 |
Tsai CT, Zulueta MML, Hung SC. Synthetic heparin and heparan sulfate: probes in defining biological functions. Current Opinion in Chemical Biology. 40: 152-159. PMID 29032302 DOI: 10.1016/J.Cbpa.2017.09.012 |
0.303 |
|
| 2017 |
Padiyar LT, Zulueta MML, Sabbavarapu NM, Hung SC. Yb(OTf)3-Catalyzed Desymmetrization of myo-Inositol-1,3,5-Orthoformate and Its Application in the Synthesis of Chiral Inositol Phosphates. The Journal of Organic Chemistry. PMID 29019688 DOI: 10.1021/Acs.Joc.7B01919 |
0.382 |
|
| 2017 |
Ho GM, Zulueta MML, Hung SC. Stereoselective one-pot synthesis of polypropionates. Nature Communications. 8: 679. PMID 28947767 DOI: 10.1038/S41467-017-00787-Y |
0.344 |
|
| 2016 |
Ho GM, Huang CJ, Li EY, Hsu SK, Wu T, Zulueta MM, Wu KB, Hung SC. Unconventional exo selectivity in thermal normal-electron-demand Diels-Alder reactions. Scientific Reports. 6: 35147. PMID 27731360 DOI: 10.1038/Srep35147 |
0.593 |
|
| 2015 |
Patil PS, Cheng TJ, Zulueta MM, Yang ST, Lico LS, Hung SC. Total synthesis of tetraacylated phosphatidylinositol hexamannoside and evaluation of its immunomodulatory activity. Nature Communications. 6: 7239. PMID 26037164 DOI: 10.1038/Ncomms8239 |
0.307 |
|
| 2015 |
Zulueta MML, Janreddy D, Hung SC. One-pot methods for the protection and assembly of sugars Israel Journal of Chemistry. 55: 347-359. DOI: 10.1002/Ijch.201400171 |
0.363 |
|
| 2014 |
Ko YC, Tsai CF, Wang CC, Dhurandhare VM, Hu PL, Su TY, Lico LS, Zulueta MM, Hung SC. Microwave-assisted one-pot synthesis of 1,6-anhydrosugars and orthogonally protected thioglycosides. Journal of the American Chemical Society. 136: 14425-31. PMID 25291402 DOI: 10.1021/Ja504804V |
0.401 |
|
| 2014 |
Chang CH, Lico LS, Huang TY, Lin SY, Chang CL, Arco SD, Hung SC. Synthesis of the heparin-based anticoagulant drug fondaparinux. Angewandte Chemie (International Ed. in English). 53: 9876-9. PMID 25044485 DOI: 10.1002/Anie.201404154 |
0.385 |
|
| 2014 |
Huang TY, Zulueta MM, Hung SC. Regioselective one-pot protection, protection-glycosylation and protection-glycosylation-glycosylation of carbohydrates: a case study with D-glucose. Organic & Biomolecular Chemistry. 12: 376-82. PMID 24263464 DOI: 10.1039/C3Ob42097C |
0.4 |
|
| 2014 |
Patil PS, Zulueta MML, Hung S. Synthesis of Phosphatidylinositol Mannosides Journal of the Chinese Chemical Society. 61: 151-162. DOI: 10.1002/Jccs.201300481 |
0.346 |
|
| 2013 |
Zulueta MM, Lin SY, Hu YP, Hung SC. Synthetic heparin and heparan sulfate oligosaccharides and their protein interactions. Current Opinion in Chemical Biology. 17: 1023-9. PMID 24182748 DOI: 10.1016/J.Cbpa.2013.10.008 |
0.341 |
|
| 2013 |
Patil PS, Lee CC, Huang YW, Zulueta MM, Hung SC. Regioselective and stereoselective benzylidene installation and one-pot protection of D-mannose. Organic & Biomolecular Chemistry. 11: 2605-12. PMID 23446759 DOI: 10.1039/C3Ob40079D |
0.374 |
|
| 2013 |
Zulueta MM, Zhong YQ, Hung SC. Synthesis of L-hexoses and their related biomolecules. Chemical Communications (Cambridge, England). 49: 3275-87. PMID 23443887 DOI: 10.1039/C3Cc37733D |
0.363 |
|
| 2013 |
Zulueta MML, Lin S, Hung S. Chemical Synthesis of Oligosaccharides Based on Heparin and Heparan Sulfate Trends in Glycoscience and Glycotechnology. 25: 141-158. DOI: 10.4052/Tigg.25.141 |
0.348 |
|
| 2012 |
Hu YP, Zhong YQ, Chen ZG, Chen CY, Shi Z, Zulueta MM, Ku CC, Lee PY, Wang CC, Hung SC. Divergent synthesis of 48 heparan sulfate-based disaccharides and probing the specific sugar-fibroblast growth factor-1 interaction. Journal of the American Chemical Society. 134: 20722-7. PMID 23240683 DOI: 10.1021/Ja3090065 |
0.3 |
|
| 2012 |
Zulueta MM, Lin SY, Lin YT, Huang CJ, Wang CC, Ku CC, Shi Z, Chyan CL, Irene D, Lim LH, Tsai TI, Hu YP, Arco SD, Wong CH, Hung SC. α-Glycosylation by D-glucosamine-derived donors: synthesis of heparosan and heparin analogues that interact with mycobacterial heparin-binding hemagglutinin. Journal of the American Chemical Society. 134: 8988-95. PMID 22587381 DOI: 10.1021/Ja302640P |
0.573 |
|
| 2012 |
Hsu Y, Lu XA, Zulueta MM, Tsai CM, Lin KI, Hung SC, Wong CH. Acyl and silyl group effects in reactivity-based one-pot glycosylation: synthesis of embryonic stem cell surface carbohydrates Lc4 and IV(2)Fuc-Lc4. Journal of the American Chemical Society. 134: 4549-52. PMID 22390569 DOI: 10.1021/Ja300284X |
0.525 |
|
| 2012 |
Luo SY, Tripathi A, Zulueta MM, Hung SC. 2-Allylphenyl glycosides as glycosyl donors for sugar coupling. Carbohydrate Research. 352: 197-201. PMID 22370177 DOI: 10.1016/J.Carres.2012.01.022 |
0.327 |
|
| 2012 |
Hung SC, Lu XA, Lee JC, Chang MD, Fang SL, Fan TC, Zulueta MM, Zhong YQ. Synthesis of heparin oligosaccharides and their interaction with eosinophil-derived neurotoxin. Organic & Biomolecular Chemistry. 10: 760-72. PMID 22143347 DOI: 10.1039/C1Ob06415K |
0.381 |
|
| 2012 |
Lu F, Lico LS, Hung S. Synthesis of a fluorogenic substrate for α-L-iduronidase Arkivoc. 2013: 13-21. DOI: 10.3998/Ark.5550190.0014.203 |
0.357 |
|
| 2012 |
Hsu C, Lee I, Lico LS, Uang B, Hung S. Synthesis of a Furanosyl-pyranone Derivative Related to the Tri-O-heterocyclic Core of Herbicidins Journal of the Chinese Chemical Society. 59: 421-425. DOI: 10.1002/Jccs.201100744 |
0.4 |
|
| 2011 |
Hsu CH, Hung SC, Wu CY, Wong CH. Toward automated oligosaccharide synthesis. Angewandte Chemie (International Ed. in English). 50: 11872-923. PMID 22127846 DOI: 10.1002/Anie.201100125 |
0.544 |
|
| 2011 |
Chung CC, Zulueta MM, Padiyar LT, Hung SC. Desymmetrization of 2,4,5,6-tetra-O-benzyl-D-myo-inositol for the synthesis of mycothiol. Organic Letters. 13: 5496-9. PMID 21919472 DOI: 10.1021/Ol202218N |
0.378 |
|
| 2011 |
Hu YP, Lin SY, Huang CY, Zulueta MM, Liu JY, Chang W, Hung SC. Synthesis of 3-O-sulfonated heparan sulfate octasaccharides that inhibit the herpes simplex virus type 1 host-cell interaction. Nature Chemistry. 3: 557-63. PMID 21697878 DOI: 10.1038/Nchem.1073 |
0.338 |
|
| 2011 |
Wang CC, Kulkarni SS, Zulueta MM, Hung SC. Synthesis of hemagglutinin-binding trisaccharides. Advances in Experimental Medicine and Biology. 705: 691-726. PMID 21618137 DOI: 10.1007/978-1-4419-7877-6_37 |
0.699 |
|
| 2011 |
Wang CC, Zulueta MM, Hung SC. Regioselective one-pot protection and protection-glycosylation of carbohydrates. Chimia. 65: 54-8. PMID 21469446 DOI: 10.2533/Chimia.2011.54 |
0.385 |
|
| 2011 |
Huang TY, Zulueta MM, Hung SC. One-pot strategies for the synthesis of the tetrasaccharide linkage region of proteoglycans. Organic Letters. 13: 1506-9. PMID 21332152 DOI: 10.1021/Ol200192D |
0.354 |
|
| 2011 |
Hsu C, Hung S, Wu C, Wong C. Auf dem Weg zur automatisierten Oligosaccharid- Synthese Angewandte Chemie. 123: 12076-12129. DOI: 10.1002/Ange.201100125 |
0.509 |
|
| 2010 |
Chang KL, Zulueta MM, Lu XA, Zhong YQ, Hung SC. Regioselective one-pot protection of D-glucosamine. The Journal of Organic Chemistry. 75: 7424-7. PMID 20936861 DOI: 10.1021/Jo101320R |
0.356 |
|
| 2010 |
Padiyar LT, Wen YS, Hung SC. Metal trifluoromethanesulfonate-catalyzed regioselective acylation of myo-inositol 1,3,5-orthoformate. Chemical Communications (Cambridge, England). 46: 5524-6. PMID 20571698 DOI: 10.1039/C0Cc00236D |
0.319 |
|
| 2010 |
Patil PS, Hung SC. Synthesis of mycobacterial triacylated phosphatidylinositol dimannoside containing an acyl lipid chain at 3-O of inositol. Organic Letters. 12: 2618-21. PMID 20443632 DOI: 10.1021/Ol1008137 |
0.382 |
|
| 2009 |
Chi FC, Kulkarni SS, Zulueta MM, Hung SC. Synthesis of alginate oligosaccharides containing L-guluronic acids. Chemistry, An Asian Journal. 4: 386-90. PMID 19097129 DOI: 10.1002/Asia.200800406 |
0.734 |
|
| 2009 |
Shie C, Tzeng Z, Wang C, Hung S. Metal Trifluoromethanesulfonate-Catalyzed Regioselective Reductive Ring Opening of Benzylidene Acetals Journal of the Chinese Chemical Society. 56: 510-523. DOI: 10.1002/Jccs.200900076 |
0.349 |
|
| 2008 |
Luo SY, Jang YJ, Liu JY, Chu CS, Liao CC, Hung SC. Carbohydrate-templated asymmetric Diels-Alder reactions of masked ortho-benzoquinones for the synthesis of chiral bicyclo[2.2.2]oct-5-en-2-ones. Angewandte Chemie (International Ed. in English). 47: 8082-5. PMID 18798203 DOI: 10.1002/Anie.200802693 |
0.607 |
|
| 2008 |
Wang CC, Kulkarni SS, Lee JC, Luo SY, Hung SC. Regioselective one-pot protection of glucose. Nature Protocols. 3: 97-113. PMID 18193026 DOI: 10.1038/Nprot.2007.493 |
0.739 |
|
| 2007 |
Wang CC, Lee JC, Luo SY, Kulkarni SS, Huang YW, Lee CC, Chang KL, Hung SC. Regioselective one-pot protection of carbohydrates. Nature. 446: 896-9. PMID 17443183 DOI: 10.1038/Nature05730 |
0.761 |
|
| 2006 |
Lu LD, Shie CR, Kulkarni SS, Pan GR, Lu XA, Hung SC. Synthesis of 48 disaccharide building blocks for the assembly of a heparin and heparan sulfate oligosaccharide library. Organic Letters. 8: 5995-8. PMID 17165913 DOI: 10.1021/Ol062464T |
0.742 |
|
| 2006 |
Luo SY, Kulkarni SS, Chou CH, Liao WM, Hung SC. A concise synthesis of tetrahydroxy-LCB, alpha-galactosyl ceramide, and 1,4-dideoxy-1,4-imino-L-ribitol via D-allosamines as key building blocks. The Journal of Organic Chemistry. 71: 1226-9. PMID 16438541 DOI: 10.1021/Jo051518U |
0.735 |
|
| 2006 |
Lee J, Pan G, Kulkarni SS, Luo S, Liao C, Hung S. 2-Allyloxyphenyl glycoside as a new and stable type of glycosyl donors Tetrahedron Letters. 47: 1621-1624. DOI: 10.1016/J.Tetlet.2005.12.127 |
0.766 |
|
| 2005 |
Kulkarni SS, Liu YH, Hung SC. Neighboring group participation of 9-anthracenylmethyl group in glycosylation: preparation of unusual C-glycosides. The Journal of Organic Chemistry. 70: 2808-11. PMID 15787575 DOI: 10.1021/Jo047794A |
0.747 |
|
| 2005 |
Shie CR, Tzeng ZH, Kulkarni SS, Uang BJ, Hsu CY, Hung SC. Cu(OTf)2 as an efficient and dual-purpose catalyst in the regioselective reductive ring opening of benzylidene acetals. Angewandte Chemie (International Ed. in English). 44: 1665-8. PMID 15685675 DOI: 10.1002/Anie.200462172 |
0.717 |
|
| 2004 |
Chou CH, Wu CS, Chen CH, Lu LD, Kulkarni SS, Wong CH, Hung SC. Regioselective glycosylation of neamine core: a facile entry to kanamycin B related analogues. Organic Letters. 6: 585-8. PMID 14961629 DOI: 10.1021/Ol0363927 |
0.781 |
|
| 2004 |
Lee JC, Chang SW, Liao CC, Chi FC, Chen CS, Wen YS, Wang CC, Kulkarni SS, Puranik R, Liu YH, Hung SC. From D-glucose to biologically potent L-hexose derivatives: synthesis of alpha-L-iduronidase fluorogenic detector and the disaccharide moieties of bleomycin A2 and heparan sulfate. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 399-415. PMID 14735509 DOI: 10.1002/Chem.200305096 |
0.739 |
|
| 2004 |
Lee JC, Lu XA, Kulkarni SS, Wen YS, Hung SC. Synthesis of heparin oligosaccharides. Journal of the American Chemical Society. 126: 476-7. PMID 14719939 DOI: 10.1021/Ja038244H |
0.757 |
|
| 2004 |
Kulkarni SS, Lee J, Hung S. Recent Advances in the Applications of D- and L-Form 1,6- Anhydrohexopyranoses for the Synthesis of Oligosaccharides and Nature Products Current Organic Chemistry. 8: 475-509. DOI: 10.2174/1385272043485800 |
0.736 |
|
| 2004 |
Kulkarni SS, Chi F, Hung S. Biologically Potent L-Hexoses and 6-Deoxy-L-Hexoses: Their Syntheses and Applications Journal of the Chinese Chemical Society. 51: 1193-1200. DOI: 10.1002/Jccs.200400175 |
0.725 |
|
| 2003 |
Tai CA, Kulkarni SS, Hung SC. Facile 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 conditions. The Journal of Organic Chemistry. 68: 8719-22. PMID 14575510 DOI: 10.1021/Jo030073B |
0.744 |
|
| 2003 |
Lu X, Chou C, Wang C, Hung S. Regioselective Esterification of Various d-Glucopyranosides: Synthesis of a Fully Protected Disaccharide Unit of Hyaluronic Acid Synlett. 2003: 1364-1366. DOI: 10.1055/S-2003-40338 |
0.34 |
|
| 2003 |
Yang W, Lu X, Kulkarni SS, Hung S. Cu(OTf)2-catalyzed Et3SiH-reductive etherification of various carbonyl compounds with trimethylsilyl ethers Tetrahedron Letters. 44: 7837-7840. DOI: 10.1016/J.Tetlet.2003.08.085 |
0.73 |
|
| 2002 |
Wang CC, Lee JC, Luo SY, Fan HF, Pai CL, Yang WC, Lu LD, Hung SC. Synthesis of biologically potent alpha1-->2-linked disaccharide derivatives via regioselective one-pot protection-glycosylation. Angewandte Chemie (International Ed. in English). 41: 2360-2. PMID 12203592 DOI: 10.1002/1521-3773(20020703)41:13<2360::Aid-Anie2360>3.0.Co;2-R |
0.33 |
|
| 2002 |
Wang CC, Luo SY, Shie CR, Hung SC. Metal trifluoromethanesulfonate-catalyzed regioselective borane-reductive ring opening of benzylidene acetals: a concise synthesis of 1,4-dideoxy-1,4-imino-L-xylitol. Organic Letters. 4: 847-9. PMID 11869143 DOI: 10.1021/Ol025567U |
0.384 |
|
| 2002 |
Hung SC, Wen YF, Chang JW, Liao CC, Uang BJ. A Highly diastereoselective synthesis of (1R)-(+)-camphor-based chiral allenes and their asymmetric hydroboration-oxidation reactions. The Journal of Organic Chemistry. 67: 1308-13. PMID 11846679 DOI: 10.1021/Jo016201I |
0.593 |
|
| 2002 |
Luo S, Thopate SR, Hsu C, Hung S. Synthesis of d-ribo-C18-phytosphingosine from d-glucosamine via the d-allosamine derivatives as key intermediates Tetrahedron Letters. 43: 4889-4892. DOI: 10.1016/S0040-4039(02)00919-X |
0.307 |
|
| 2002 |
Lee J, Tai C, Hung S. Sc(OTf)3-catalyzed acetolysis of 1,6-anhydro-β-hexopyranoses and solvent-free per-acetylation of hexoses Tetrahedron Letters. 43: 851-855. DOI: 10.1016/S0040-4039(01)02253-5 |
0.304 |
|
| 2001 |
Hung SC, Thopate SR, Chi FC, Chang SW, Lee JC, Wang CC, Wen YS. 1,6-anhydro-beta-l-hexopyranoses as potent synthons in the synthesis of the disaccharide units of bleomycin A(2) and heparin. Journal of the American Chemical Society. 123: 3153-4. PMID 11457034 DOI: 10.1021/Ja003508A |
0.311 |
|
| 2001 |
Hung SC, Thopate SR, Puranik R. Synthesis of 6-deoxy-L-idose and L-acovenose from 1,2: 5,6-di-O-isopropylidene-alpha-D-glucofuranose. Carbohydrate Research. 331: 369-74. PMID 11398979 DOI: 10.1016/S0008-6215(01)00058-1 |
0.345 |
|
| 2001 |
Hung SC, Thopate SR, Wang CC. Regioselective and stereoselective benzoylation of 2-N-protected 4,6-O-ketal derivatives of D-glucosamines with 1-(benzoyloxy)benzotriazole. Carbohydrate Research. 330: 177-82. PMID 11217970 DOI: 10.1016/S0008-6215(00)00282-2 |
0.351 |
|
| 2001 |
Hung S, Wang C, Chang S, Chen C. 1,6-Anhydro-β-l-hexopyranoses as valuable building blocks toward the synthesis of l-gulosamine and l-altrose derivatives Tetrahedron Letters. 42: 1321-1324. DOI: 10.1016/S0040-4039(00)02237-1 |
0.312 |
|
| 2000 |
Hung S, Puranik R, Chi F. Novel synthesis of 1,2:3,5-di-O-isopropylidene-β-l-idofuranoside and its derivatives at C6 Tetrahedron Letters. 41: 77-80. DOI: 10.1016/S0040-4039(99)02004-3 |
0.366 |
|
| 2000 |
Hung S, Wang C, Thopate SR. Efficient synthesis of l-altrose and l-mannose Tetrahedron Letters. 41: 3119-3122. DOI: 10.1016/S0040-4039(00)00363-4 |
0.337 |
|
| 2000 |
Hung S, Chen C. Efficient Synthesis of 1,2,3,4,6-Penta-O-acetyl-L-idopyranose Journal of the Chinese Chemical Society. 47: 1257-1262. DOI: 10.1002/Jccs.200000173 |
0.365 |
|
| 1997 |
Murray BW, Wittmann V, Burkart MD, Hung SC, Wong CH. Mechanism of human alpha-1,3-fucosyltransferase V: glycosidic cleavage occurs prior to nucleophilic attack. Biochemistry. 36: 823-31. PMID 9020780 DOI: 10.1021/Bi962284Z |
0.638 |
|
| 1997 |
Uang B, Po S, Hung S, Liu H, Hsu C, Lin Y, Chang J. Asymmetric synthesis employing chiral ketones as templates Pure and Applied Chemistry. 69: 615-620. DOI: 10.1351/Pac199769030615 |
0.373 |
|
| 1997 |
Burkart MD, Zhang Z, Hung SC, Wong CH. A new method for the synthesis of fluoro-carbohydrates and glycosides using selectfluor Journal of the American Chemical Society. 119: 11743-11746. DOI: 10.1021/Ja9723904 |
0.694 |
|
| 1997 |
Wong C, Moris-Varas F, Hung S, Marron TG, Lin C, Gong KW, Weitz-Schmidt G. Small Molecules as Structural and Functional Mimics of Sialyl Lewis X Tetrasaccharide in Selectin Inhibition: A Remarkable Enhancement of Inhibition by Additional Negative Charge and/or Hydrophobic Group Journal of the American Chemical Society. 119: 8152-8158. DOI: 10.1021/Ja970920Q |
0.551 |
|
| 1997 |
Hung S, Lin C, Wong C. One-pot synthesis of 1-allyl- and 1-allenyl-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glycosides from methyl tetra-O-benzyl-α-D-glycosides Tetrahedron Letters. 38: 5419-5422. DOI: 10.1016/S0040-4039(97)01204-5 |
0.566 |
|
| 1996 |
Alper PB, Hung S, Wong C. Metal catalyzed diazo transfer for the synthesis of azides from amines Tetrahedron Letters. 37: 6029-6032. DOI: 10.1016/0040-4039(96)01307-X |
0.541 |
|
| 1996 |
Hung SC, Wong CH. Synthesis of glycosyl chlorides with acid-labile protecting groups Tetrahedron Letters. 37: 4903-4906. DOI: 10.1016/0040-4039(96)01006-4 |
0.582 |
|
| 1996 |
Hung S, Wong C. Samarium Diiodide Mediated Coupling of Glycosyl Phosphates with Carbon Radical or Anion Acceptors—Synthesis of C‐Glycosides Angewandte Chemie. 35: 2671-2674. DOI: 10.1002/Anie.199626711 |
0.497 |
|
| 1996 |
Hung S, Wong C. Samariumdiiodid‐vermittelte Kupplung von Glycosylphosphaten mit Kohlenstoffradikal‐ oder ‐anion‐Acceptoren – Synthese von C‐Glycosiden Angewandte Chemie. 108: 2829-2832. DOI: 10.1002/Ange.19961082225 |
0.509 |
|
| 1994 |
Hung S, Liao C. Diels‐Alder Reactions and Synthetic Application of 8‐Trimethylsilyloxy‐1,4‐dioxaspiro[4.5]deca‐6,8‐diene. A Formal Synthesis of (±)‐Compaclin Journal of the Chinese Chemical Society. 41: 817-828. DOI: 10.1002/Jccs.199400114 |
0.583 |
|
| 1994 |
Hung S, Liao C. Double Michael Additions of Lithium Enolate of 1,4‐Dioxaspiro[4.5]dec‐6‐en‐8‐One to Acrylates Journal of the Chinese Chemical Society. 41: 191-194. DOI: 10.1002/Jccs.199400027 |
0.597 |
|
| 1993 |
Hung S, Liao C. A formal synthesis of (±)-compactin Journal of the Chemical Society, Chemical Communications. 1457-1458. DOI: 10.1039/C39930001457 |
0.567 |
|
| 1991 |
Hung S, Liao C. Diels-alder reactions of 8-trimethylsilyloxy-1,4-dioxaspiro[4,5]deca-6,8-diene Tetrahedron Letters. 32: 4011-4014. DOI: 10.1016/0040-4039(91)80614-C |
0.57 |
|
| Show low-probability matches. |
