| Year |
Citation |
Score |
| 2020 |
Chang C, Geng J, Liu Y, Du Y, Liu J, Dong Z. Stereoselective Total Synthesis of Arundinolides A and B Synthesis. 52: 1576-1584. DOI: 10.1055/S-0039-1691699 |
0.428 |
|
| 2020 |
Lv Q, Chang C, Li Y, Du Y, Liu J. Stereoselective synthesis of (−)-protulactone A Tetrahedron. 76: 131290. DOI: 10.1016/J.Tet.2020.131290 |
0.412 |
|
| 2019 |
He P, Zhao C, Lu J, Zhang Y, Fang M, Du Y. Correction to "Synthesis of 5-Thio-α-GalCer Analogues with Fluorinated Acyl Chain on Lipid Residue and Their Biological Evaluation". Acs Medicinal Chemistry Letters. 10: 394. PMID 30891148 DOI: 10.1021/Acsmedchemlett.9B00057 |
0.303 |
|
| 2019 |
Sun X, Wei D, Liu W, Geng J, Liu J, Du Y. Formation of novel disinfection by-products chlorinated benzoquinone, phenyl benzoquinones and polycyclic aromatic hydrocarbons during chlorination treatment on UV filter 2,4-dihydroxybenzophenone in swimming pool water. Journal of Hazardous Materials. 367: 725-733. PMID 30685680 DOI: 10.1016/J.Jhazmat.2019.01.008 |
0.315 |
|
| 2019 |
Geng J, Ren Q, Chang C, Xie X, Liu J, Du Y. Synthesis and biological activities of petrosiols B and D Rsc Advances. 9: 10253-10263. DOI: 10.1039/C9Ra01166H |
0.371 |
|
| 2019 |
Chang C, Geng J, Du Y, Lv Q, Dong Z, Liu J. Divergent total synthesis of aspinolides B, E and J Tetrahedron. 75: 3933-3938. DOI: 10.1016/J.Tet.2019.06.015 |
0.419 |
|
| 2018 |
Qiao J, Zhao C, Liu J, Du Y. Design and synthesis of selenazole-substituted ritonavir analogs. Bioorganic & Medicinal Chemistry Letters. PMID 29934245 DOI: 10.1016/J.Bmcl.2018.06.027 |
0.331 |
|
| 2018 |
Liu Y, He P, Zhang Y, Zhang X, Liu J, Du Y. One-pot Enantiomeric Synthesis of Thiazole-containing Amino Acids: Total Synthesis of Venturamides A and B. The Journal of Organic Chemistry. PMID 29533619 DOI: 10.1021/Acs.Joc.8B00244 |
0.385 |
|
| 2018 |
Gao Y, Liu J, Qiao J, Liu Y, He P, Du Y. Stereoselective synthesis of (−)-synargentolide B Tetrahedron Letters. 59: 291-294. DOI: 10.1016/J.Tetlet.2017.12.039 |
0.401 |
|
| 2018 |
Qiao J, Liu Y, Du Y. Method to build 2,4-substituted selenazole from β-azido diselenide and carboxylic acid: A formal synthesis of selenazofurin Tetrahedron. 74: 3061-3068. DOI: 10.1016/J.Tet.2018.05.010 |
0.387 |
|
| 2018 |
Shang C, Cai C, Zhao C, Du Y. Synthesis and anti-inflammatory activity of gold-nanoparticle bearing a dermatan sulfate disaccharide analog Chinese Chemical Letters. 29: 81-83. DOI: 10.1016/J.Cclet.2017.06.010 |
0.534 |
|
| 2017 |
Liu Y, Du Y, Li Z, Xie Y, He P, Qiao J, Fan X. Efficient One-Pot Synthesis of 2,4-Disubstituted Thiazoles and Dimeric Thiazoles Directly from Acyl Chlorides and β-Azido Disulfides Synthesis. 49: 4876-4886. DOI: 10.1055/S-0036-1590810 |
0.422 |
|
| 2017 |
Liu J, Gao Y, Wang L, Du Y. Chiron approach for the total synthesis of (+)-synargentolide B Tetrahedron. 73: 6443-6447. DOI: 10.1016/J.Tet.2017.09.041 |
0.404 |
|
| 2016 |
Liu W, Wei D, Liu Q, Du Y. Transformation pathways and acute toxicity variation of 4-hydroxyl benzophenone in chlorination disinfection process. Chemosphere. 154: 491-498. PMID 27085063 DOI: 10.1016/J.Chemosphere.2016.04.005 |
0.305 |
|
| 2015 |
Bi J, Zhao C, Cui W, Zhang C, Shan Q, Du Y. Synthesis and affinities of C3-symmetric thioglycoside-containing trimannosides. Carbohydrate Research. 412: 56-65. PMID 26047464 DOI: 10.1016/J.Carres.2015.05.001 |
0.331 |
|
| 2015 |
Sun X, Liu Y, Liu J, Gu G, Du Y. Synthesis and structural reconfirmation of bacillamide B. Organic & Biomolecular Chemistry. 13: 4271-7. PMID 25758024 DOI: 10.1039/C5Ob00093A |
0.385 |
|
| 2015 |
Li J, Zhao C, Liu J, Du Y. Total synthesis of proposed cephalosporolides H and I Tetrahedron. 71: 3885-3889. DOI: 10.1016/J.Tet.2015.04.025 |
0.339 |
|
| 2014 |
Liu Y, Sun X, Zhang X, Liu J, Du Y. Concise synthesis of 2,4-disubstituted thiazoles from β-azido disulfides and carboxylic acids or anhydrides: asymmetric synthesis of cystothiazole C. Organic & Biomolecular Chemistry. 12: 8453-61. PMID 25223403 DOI: 10.1039/C4Ob01460J |
0.411 |
|
| 2014 |
Gao Y, Shan Q, Liu J, Wang L, Du Y. The first convergent total synthesis of penarolide sulfate A2, a novel α-glucosidase inhibitor. Organic & Biomolecular Chemistry. 12: 2071-9. PMID 24519177 DOI: 10.1039/C3Ob42364F |
0.342 |
|
| 2014 |
Li M, Wei D, Zhao H, Du Y. Genotoxicity of quinolones: substituents contribution and transformation products QSAR evaluation using 2D and 3D models. Chemosphere. 95: 220-6. PMID 24080009 DOI: 10.1016/J.Chemosphere.2013.09.002 |
0.306 |
|
| 2014 |
Zhang C, Liu J, Du Y. Total synthesis of ribisin A Tetrahedron Letters. 55: 959-961. DOI: 10.1016/J.Tetlet.2013.12.052 |
0.393 |
|
| 2014 |
Wang L, Zhang X, Liu J, Du Y. Total synthesis of (−)-petrosiol E Tetrahedron. 70: 8231-8235. DOI: 10.1016/J.Tet.2014.09.030 |
0.395 |
|
| 2014 |
Wang L, Gao Y, Liu J, Cai C, Du Y. Stereoselective total synthesis of cochliomycin A Tetrahedron. 70: 2616-2620. DOI: 10.1016/J.Tet.2014.03.001 |
0.577 |
|
| 2014 |
Gao Y, Liu J, Wang L, Xiao M, Du Y. Total Syntheses of Cochliomycin B and Zeaenol European Journal of Organic Chemistry. 2014: 2092-2098. DOI: 10.1002/Ejoc.201301613 |
0.366 |
|
| 2013 |
Li L, Wei D, Wei G, Du Y. Transformation of cefazolin during chlorination process: products, mechanism and genotoxicity assessment. Journal of Hazardous Materials. 262: 48-54. PMID 24007998 DOI: 10.1016/J.Jhazmat.2013.08.029 |
0.308 |
|
| 2013 |
Xiao M, Wei D, Yin J, Wei G, Du Y. Transformation mechanism of benzophenone-4 in free chlorine promoted chlorination disinfection. Water Research. 47: 6223-33. PMID 23953088 DOI: 10.1016/J.Watres.2013.07.043 |
0.328 |
|
| 2013 |
Zhao H, Wei D, Li M, Du Y. Substituent contribution to the genotoxicity of benzophenone-type UV filters. Ecotoxicology and Environmental Safety. 95: 241-6. PMID 23790521 DOI: 10.1016/J.Ecoenv.2013.05.036 |
0.304 |
|
| 2013 |
Zhang X, Liu J, Liu Y, Du Y. An efficient preparation of 2-alkyl-oxazoles from 2-iodooxazoles Tetrahedron Letters. 54: 4045-4048. DOI: 10.1016/J.Tetlet.2013.05.088 |
0.393 |
|
| 2013 |
Zhang C, Liu J, Du Y. A concise total synthesis of (+)-pyrenolide D Tetrahedron Letters. 54: 3278-3280. DOI: 10.1016/J.Tetlet.2013.04.044 |
0.411 |
|
| 2013 |
Zhang C, Ma X, Du Y. Synthesis of Neu5Ac-α-C-galactopyranosyl-functionalized magnetic nanoparticles via click chemistry Tetrahedron. 69: 7300-7307. DOI: 10.1016/J.Tet.2013.06.086 |
0.312 |
|
| 2013 |
Zhang X, Liu J, Sun X, Du Y. An efficient cis-reduction of alkyne to alkene in the presence of a vinyl iodide: stereoselective synthesis of the C22–C31 fragment of leiodolide A Tetrahedron. 69: 1553-1558. DOI: 10.1016/J.Tet.2012.12.008 |
0.373 |
|
| 2012 |
Liu J, Liu Y, Zhang X, Zhang C, Gao Y, Wang L, Du Y. Total synthesis of (-)-orthodiffenes A and C. The Journal of Organic Chemistry. 77: 9718-23. PMID 23051061 DOI: 10.1021/Jo301829P |
0.421 |
|
| 2012 |
Liu Y, Liu J, Qi X, Du Y. One-pot synthesis of 2,4-disubstituted thiazoline from β-azido disulfide and carboxylic acid. The Journal of Organic Chemistry. 77: 7108-13. PMID 22835091 DOI: 10.1021/Jo301030K |
0.379 |
|
| 2012 |
Liu J, Zhang X, Liu Y, Bi J, Du Y. Total synthesis of (−)-isoaltholactone Science China Chemistry. 56: 928-932. DOI: 10.1007/S11426-012-4823-3 |
0.41 |
|
| 2011 |
Lv X, Yu S, Wang J, Du Y. Synthesis of stryphnoside A, a triterpene saponin isolated from the pericarps of Stryphnodendron fissuratum. Carbohydrate Research. 346: 1786-91. PMID 21798521 DOI: 10.1016/J.Carres.2011.06.006 |
0.357 |
|
| 2011 |
Wei G, Wang J, Du Y. Total synthesis of solamargine. Bioorganic & Medicinal Chemistry Letters. 21: 2930-3. PMID 21482107 DOI: 10.1016/J.Bmcl.2011.03.064 |
0.379 |
|
| 2010 |
Cai C, Wei G, Du Y. Methyl 2,3-di-O-acetyl-4-O-levulinoyl-1-O-(2,2,2-trichloro-2-imino-ethyl)-l-ido-pyran-osiduronate. Acta Crystallographica. Section E, Structure Reports Online. 66: o949. PMID 21580753 DOI: 10.1107/S1600536810010895 |
0.522 |
|
| 2010 |
Zhang L, Wei G, Du Y. Total synthesis of apigenin-4'-yl 2-O-(p-coumaroyl)-β-D-glucopyranoside. Carbohydrate Research. 345: 2714-7. PMID 21055731 DOI: 10.1016/J.Carres.2010.10.008 |
0.408 |
|
| 2010 |
Lv X, Cheng S, Wei G, Du Y. Synthesis of the pentasaccharide repeating unit of Escherichia coli O128 antigen. Carbohydrate Research. 345: 2272-6. PMID 20804976 DOI: 10.1016/J.Carres.2010.07.025 |
0.348 |
|
| 2010 |
Cai C, Liu J, Du Y, Linhardt RJ. Stereoselective total synthesis of (-)-cleistenolide. The Journal of Organic Chemistry. 75: 5754-6. PMID 20704451 DOI: 10.1021/Jo101059E |
0.639 |
|
| 2010 |
POLAT T, DU Y, LINHARDT RJ. ChemInform Abstract: A General Method for the Stereospecific Synthesis of C-Glycosides of Ulosonic Acids by Samarium-Mediated Reductive Dechlorination. Cheminform. 30: no-no. DOI: 10.1002/chin.199908234 |
0.397 |
|
| 2009 |
Zhang L, Wei G, Du Y. Synthesis of Neu5Ac-Gal-functionalized gold glyconanoparticles. Carbohydrate Research. 344: 2083-7. PMID 19664758 DOI: 10.1016/J.Carres.2009.06.039 |
0.361 |
|
| 2009 |
Zhang Q, Gao F, Peng H, Cheng H, Liu Y, Tang J, Thompson J, Wei G, Zhang J, Du Y, Yan J, Gao GF. Crystal structures of Streptococcus suis mannonate dehydratase (ManD) and its complex with substrate: genetic and biochemical evidence for a catalytic mechanism. Journal of Bacteriology. 191: 5832-7. PMID 19617363 DOI: 10.1128/Jb.00599-09 |
0.306 |
|
| 2009 |
Huang X, Cheng S, Du Y, Bing F. Synthesis of oleanolic acid saponins mimicking components of Chinese folk medicine Di Wu. Carbohydrate Research. 344: 1153-8. PMID 19467649 DOI: 10.1016/J.Carres.2009.04.005 |
0.342 |
|
| 2009 |
Cheng S, Du Y, Ma B, Tan D. Total synthesis of a furostan saponin, timosaponin BII Organic & Biomolecular Chemistry. 7: 3112. DOI: 10.1039/B905091D |
0.36 |
|
| 2008 |
Wei G, Lv X, Du Y. FeCl3-catalyzed alpha-glycosidation of glycosamine pentaacetates. Carbohydrate Research. 343: 3096-9. PMID 18828995 DOI: 10.1016/J.Carres.2008.09.003 |
0.307 |
|
| 2008 |
Cheng S, Du Y, Bing F, Zhang G. Synthesis of flaccidoside II, a bidesmosidic triterpene saponin isolated from Chinese folk medicine Di Wu. Carbohydrate Research. 343: 462-9. PMID 18070618 DOI: 10.1016/J.Carres.2007.11.015 |
0.347 |
|
| 2008 |
Wei G, Zhang L, Cai C, Cheng S, Du Y. Selective cleavage of sugar anomeric O-acyl groups using FeCl3·6H2O Tetrahedron Letters. 49: 5488-5491. DOI: 10.1016/J.Tetlet.2008.07.035 |
0.507 |
|
| 2007 |
Chen Q, Du Y. Synthesis of sporiolide B from D-glucal. Carbohydrate Research. 342: 1405-11. PMID 17517381 DOI: 10.1016/J.Carres.2007.04.013 |
0.408 |
|
| 2007 |
Du Y, Liu J, Linhardt RJ. Facile synthesis of (+/-)-paeonilide. The Journal of Organic Chemistry. 72: 3952-4. PMID 17411097 DOI: 10.1021/Jo0701278 |
0.501 |
|
| 2007 |
Cheng L, Chen Q, Liu J, Du Y. Synthesis of a fluorescence-labeled K30 antigen repeating unit using click chemistry. Carbohydrate Research. 342: 975-81. PMID 17306240 DOI: 10.1016/J.Carres.2007.01.015 |
0.33 |
|
| 2006 |
Du Y, Chen Q, Linhardt RJ. The first total synthesis of sporiolide A. The Journal of Organic Chemistry. 71: 8446-51. PMID 17064018 DOI: 10.1021/Jo0615504 |
0.533 |
|
| 2006 |
Liu J, Du Y, Dong X, Meng S, Xiao J, Cheng L. Stereoselective synthesis of jaspine B from D-xylose. Carbohydrate Research. 341: 2653-7. PMID 16973139 DOI: 10.1016/J.Carres.2006.08.011 |
0.38 |
|
| 2006 |
Mousa SA, Feng X, Xie J, Du Y, Hua Y, He H, O'Connor L, Linhardt RJ. Synthetic oligosaccharide stimulates and stabilizes angiogenesis: structure-function relationships and potential mechanisms. Journal of Cardiovascular Pharmacology. 48: 6-13. PMID 16954815 DOI: 10.1097/01.Fjc.0000238591.90062.62 |
0.394 |
|
| 2006 |
Du Y, Liu J, Linhardt RJ. Stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine B) from D-xylose. The Journal of Organic Chemistry. 71: 1251-3. PMID 16438548 DOI: 10.1021/Jo051644Y |
0.459 |
|
| 2006 |
Hua Y, Xiao J, Huang Y, Du Y. Synthesis of the pentasaccharide repeating unit of lactosillan [correction of latosillan]. Carbohydrate Research. 341: 191-7. PMID 16332360 DOI: 10.1016/J.Carres.2005.11.007 |
0.339 |
|
| 2006 |
Chen Q, Du Y. The first total synthesis of sporiolide B Tetrahedron Letters. 47: 8489-8492. DOI: 10.1016/J.Tetlet.2006.09.145 |
0.396 |
|
| 2006 |
Du Y, Wei G, Cheng S, Hua Y, Linhardt RJ. HClO4–SiO2 catalyzed glycosylation using sugar trichloroacetimidates as glycosyl donors Tetrahedron Letters. 47: 307-310. DOI: 10.1016/J.Tetlet.2005.11.025 |
0.459 |
|
| 2005 |
Chen Q, Yang F, Du Y. Synthesis of a C3-symmetric (1-->6)-N-acetyl-beta-D-glucosamine octadecasaccharide using click chemistry. Carbohydrate Research. 340: 2476-82. PMID 16169535 DOI: 10.1016/J.Carres.2005.08.013 |
0.361 |
|
| 2005 |
Wei L, Wei G, Zhang H, Wang PG, Du Y. Synthesis of new, potent avermectin-like insecticidal agents. Carbohydrate Research. 340: 1583-90. PMID 15922315 DOI: 10.1016/J.Carres.2005.04.019 |
0.372 |
|
| 2004 |
Gu G, Du Y, Linhardt RJ. Facile synthesis of saponins containing 2,3-branched oligosaccharides by using partially protected glycosyl donors. The Journal of Organic Chemistry. 69: 5497-500. PMID 15287807 DOI: 10.1021/Jo0493929 |
0.518 |
|
| 2004 |
Hua Y, Du Y, Yu G, Chu S. Synthesis and biological activities of octyl 2,3-di-O-sulfo-alpha-L-fucopyranosyl-(1-->3)-2-O-sulfo-alpha-L-fucopyranosyl-(1-->4)-2,3-di-O-sulfo-alpha-L-fucopyranosyl-(1-->3)-2-O-sulfo-alpha-L-fucopyranosyl-(1-->4)-2,3-di-O-sulfo-beta-L-fucopyranoside. Carbohydrate Research. 339: 2083-90. PMID 15280053 DOI: 10.1016/J.Carres.2004.06.006 |
0.319 |
|
| 2004 |
Gu G, Wei G, Du Y. Synthesis of a 6(V)-sulfated mannopentasaccharide analogue related to PI-88. Carbohydrate Research. 339: 1155-62. PMID 15063205 DOI: 10.1016/J.Carres.2004.01.020 |
0.343 |
|
| 2004 |
Du Y, Wei G, Linhardt RJ. Total synthesis of quercetin 3-sophorotrioside. The Journal of Organic Chemistry. 69: 2206-9. PMID 15058976 DOI: 10.1021/Jo035722Y |
0.477 |
|
| 2004 |
Hua Y, Gu G, Du Y. Synthesis and biological activities of octyl 2,3,4-tri-O-sulfo-alpha-L-fucopyranosyl-(1-->3)-2,4-di-O-sulfo-alpha-L-fucopyranosyl-(1-->3)-2,4-di-O-sulfo-alpha-L-fucopyranosyl-(1-->3)-2,4-di-O-sulfo-beta-L-fucopyranoside. Carbohydrate Research. 339: 867-72. PMID 14980830 DOI: 10.1016/J.Carres.2003.12.014 |
0.322 |
|
| 2004 |
Wei G, Du Y, Linhardt RJ. New potent insecticidal agent: 4′-fucosyl avermectin derivative Tetrahedron Letters. 45: 6895-6898. DOI: 10.1016/J.Tetlet.2004.07.092 |
0.489 |
|
| 2004 |
Du Y, Gu G, Hua Y, Wei G, Ye X, Yu G. Synthesis and antitumor activities of glucan derivatives Tetrahedron. 60: 6345-6351. DOI: 10.1016/J.Tet.2004.05.086 |
0.329 |
|
| 2003 |
Kang Y, Mei Y, Du Y, Jin Z. Total synthesis of the highly potent anti-HIV natural product daurichromenic acid along with its two chromane derivatives, rhododaurichromanic acids A and B. Organic Letters. 5: 4481-4. PMID 14602030 DOI: 10.1021/Ol030109M |
0.348 |
|
| 2003 |
Du Y, Gu G, Wei G, Hua Y, Linhardt RJ. Synthesis of saponins using partially protected glycosyl donors. Organic Letters. 5: 3627-30. PMID 14507189 DOI: 10.1021/Ol035353S |
0.498 |
|
| 2003 |
Gu G, Du Y, Hu H, Jin C. Synthesis of 2-chloro-4-nitrophenyl alpha-L-fucopyranoside: a substrate for alpha-L-fucosidase (AFU). Carbohydrate Research. 338: 1603-7. PMID 12860431 DOI: 10.1016/S0008-6215(03)00244-1 |
0.323 |
|
| 2003 |
Yang F, Hua Y, Du Y. Synthesis of biantennary beta-D-(1-->6) glucosamine oligosaccharides. Carbohydrate Research. 338: 1313-8. PMID 12791285 DOI: 10.1016/S0008-6215(03)00170-8 |
0.329 |
|
| 2003 |
Yang F, Du Y. A practical synthesis of a (1-->6)-linked beta-D-glucosamine nonasaccharide. Carbohydrate Research. 338: 495-502. PMID 12668105 DOI: 10.1016/S0008-6215(02)00494-9 |
0.337 |
|
| 2003 |
Wei G, Gu G, Du Y. Silver Triflate. A Mild Alternative Catalyst for Glycosylation Conditions Using Trichloroacetimidates as Glycosyl Donors Journal of Carbohydrate Chemistry. 22: 385-393. DOI: 10.1081/Car-120025325 |
0.308 |
|
| 2003 |
He H, Gu G, Du Y. Synthesis of Laminarin Oligosaccharide Derivatives Havingd‐Arabinofuranosyl Side‐Chains Journal of Carbohydrate Chemistry. 22: 275-283. DOI: 10.1081/Car-120023470 |
0.362 |
|
| 2003 |
Du Y, Wei G, Linhardt RJ. The first total synthesis of calabricoside A Tetrahedron Letters. 44: 6887-6890. DOI: 10.1016/S0040-4039(03)01706-4 |
0.486 |
|
| 2002 |
He H, Yang F, Du Y. Synthesis of natural beta-D-(1-->3)-glucopyranosyl oligosaccharides. Carbohydrate Research. 337: 1673-8. PMID 12423970 DOI: 10.1016/S0008-6215(02)00276-8 |
0.334 |
|
| 2002 |
Gu G, Du Y, Pan J. Concise synthesis of a buffalo milk pentasaccharide derivative. Carbohydrate Research. 337: 1313-7. PMID 12151212 DOI: 10.1016/S0008-6215(02)00131-3 |
0.378 |
|
| 2002 |
Yang F, Du Y. Synthesis of oligosaccharide derivatives related to those from sanqi, a Chinese herbal medicine from Panax notoginseng. Carbohydrate Research. 337: 485-91. PMID 11890886 DOI: 10.1016/S0008-6215(02)00013-7 |
0.317 |
|
| 2002 |
Gu G, Yang F, Du Y, Kong F. Synthesis of a hexasaccharide that relates to the arabinogalactan epitope. Carbohydrate Research. 336: 99-106. PMID 11689180 DOI: 10.1016/S0008-6215(01)00259-2 |
0.349 |
|
| 2002 |
Gu G, Du Y. Synthesis of a pentasaccharide derivative corresponding to a triterpenoid saponin isolated from Spergularia ramosa Journal of the Chemical Society-Perkin Transactions 1. 2075-2079. DOI: 10.1039/B205106K |
0.338 |
|
| 2002 |
Yang F, He H, Du Y. Synthesis of (1→6)-β-d-glucosamine hexasaccharide, a potential antitumor and immunostimulating agent Tetrahedron Letters. 43: 7561-7563. DOI: 10.1016/S0040-4039(02)01812-9 |
0.368 |
|
| 2001 |
Zhang M, Du Y, Kong F. Practical synthesis of a tetrasaccharide derivative corresponding to ristomycin A and ristocetin A. Carbohydrate Research. 330: 319-24. PMID 11270810 DOI: 10.1016/S0008-6215(00)00303-7 |
0.342 |
|
| 2001 |
Pan Q, Du Y, Kong* F, Pan J, Lü M. SYNTHESIS OF 3-O-ARABINOSYLATED (1→6)-β-D-GALACTAN EPITOPES Journal of Carbohydrate Chemistry. 20: 297-306. DOI: 10.1081/Car-100104865 |
0.367 |
|
| 2001 |
Du Y, Zhang M, Yang F, Gu G. A simple access to 3,6-branched oligosaccharides: Synthesis of a glycopeptide derivative that relates to Lycium barbarum L. Journal of the Chemical Society-Perkin Transactions 1. 3122-3127. DOI: 10.1039/B108399F |
0.362 |
|
| 2001 |
Du Y, Zhang M, Kong F. An efficient synthesis of julibrosides related to neosaponin Journal of the Chemical Society-Perkin Transactions 1. DOI: 10.1039/B009955O |
0.341 |
|
| 2001 |
Du Y, Zhang M, Kong F. Efficient and practical syntheses of three pentasaccharides core structures corresponding to N -glycans Tetrahedron. 57: 1757-1763. DOI: 10.1016/S0040-4020(00)01161-3 |
0.353 |
|
| 2001 |
Zhang M, Du Y, Kong F. Corrigendum to “Practical synthesis of a tetrasaccharide derivative corresponding to ristomycin A and ristocetin A” Carbohydrate Research. 334: 251. DOI: 10.1016/S0008-6215(01)00185-9 |
0.386 |
|
| 2000 |
Du Y, Zhang M, Kong F. Highly efficient and practical synthesis of 3,6-branched oligosaccharides. Organic Letters. 2: 3797-3800. PMID 11101422 DOI: 10.1021/Ol000243W |
0.381 |
|
| 2000 |
Du Y, Pan Q, Kong F. An efficient and concise regioselective synthesis of α-(1→5)-linked l-arabinofuranosyl oligosaccharides Carbohydrate Research. 329: 17-24. PMID 11086682 DOI: 10.1016/S0008-6215(00)00159-2 |
0.381 |
|
| 2000 |
Wang Q, Wolff M, Polat T, Du Y, Linhardt RJ. Inhibition of neuraminidase with neuraminic acid C-glycosides. Bioorganic & Medicinal Chemistry Letters. 10: 941-4. PMID 10853664 DOI: 10.1016/S0960-894X(00)00132-3 |
0.434 |
|
| 1999 |
Du Y, Pan Q, Kong F. Synthesis of a tetrasaccharide representing a minimal epitope of an arabinogalactan. Carbohydrate Research. 323: 28-35. PMID 10782282 DOI: 10.1016/S0008-6215(99)00252-9 |
0.378 |
|
| 1999 |
Du Y, Kong F. The Regio- and Stereoselective Synthesis of Rhamnose-Containing OligosaccharidesViaSugar-Sugar Orthoester Formation and Rearrangement Journal of Carbohydrate Chemistry. 18: 655-666. DOI: 10.1080/07328309908544027 |
0.413 |
|
| 1999 |
Du Y, Pan Q, Kong F. Regio- and Stereoselective Synthesis of 1 → 5-Linked α-l-Arabinofuranosyl Oligosaccharides Synlett. 1999: 1648-1650. DOI: 10.1055/S-1999-3170 |
0.349 |
|
| 1999 |
Bazin HG, Du Y, Polat T, Linhardt RJ. Synthesis of a versatile neuraminic acid 'C'-disaccharide precursor for the synthesis of C-glycoside analogues of gangliosides Journal of Organic Chemistry. 64: 7254-7259. DOI: 10.1021/Jo990564P |
0.484 |
|
| 1998 |
Du Y, Polat T, Linhardt RJ. The stereospecific synthesis of KDN α-C-glycosides by samarium mediated reductive desulfonylation of glycosyl phenylsulfone Tetrahedron Letters. 39: 5007-5010. DOI: 10.1016/S0040-4039(98)00980-0 |
0.329 |
|
| 1998 |
Du Y, Linhardt RJ, Vlahov IR. Recent advances in stereoselective c-glycoside synthesis Tetrahedron. 54: 9913-9959. DOI: 10.1016/S0040-4020(98)00405-0 |
0.47 |
|
| 1998 |
Du Y, Linhardt RJ. Stereospecific synthesis of α-C-glycosyl derivatives (“α-C-glycosides”) of N-acetylneuraminic acid by samarium-mediated reductive desulfonylation of a glycosyl phenylsulfone Carbohydrate Research. 308: 161-164. DOI: 10.1016/S0008-6215(98)00054-8 |
0.484 |
|
| 1997 |
Du Y, Lin J, Linhardt RJ. Regioselective Synthesis of L-Idopyranuronic Acid Derivatives: Intermolecular Aglycon Transfer of Dithioacetal Under Standard Glycosylation Conditions Journal of Carbohydrate Chemistry. 16: 1327-1344. DOI: 10.1080/07328309708005753 |
0.484 |
|
| 1996 |
Du Y, Kong F. Synthesis and Glycosidic Reaction of 1,2-Anhydromanno-, Lyxo-, Gluco-, and Xylofuranose Perbenzyl Ethers Journal of Carbohydrate Chemistry. 15: 797-817. DOI: 10.1080/07328309608005693 |
0.435 |
|
| 1996 |
Du Y, Mao W, Kong F. Synthesis of 1,2-anhydro-d-altropyranose and -d-allopyranose benzyl ethers Carbohydrate Research. 282: 315-323. DOI: 10.1016/0008-6215(95)00391-6 |
0.341 |
|
| 1995 |
Du Y, Kong F. Synthesis and unusual glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-α-d-fucopyranose Carbohydrate Research. 275: 413-420. PMID 8529233 DOI: 10.1016/0008-6215(95)00160-U |
0.399 |
|
| 1995 |
Du Y, Kong F. Stereoselective glycosidic coupling reactions of fully benzylated 1, 2-anhydro sugars with v-tosyl- or n-benzyloxycarbonyl-l-serine methyl ester Journal of Carbohydrate Chemistry. 14: 341-352. DOI: 10.1080/07328309508002076 |
0.41 |
|
| 1995 |
Du Y, Kong F. A facile synthesis of 1,2-anhydroglycofuranose benzyl ethers Tetrahedron Letters. 36: 427-430. DOI: 10.1016/0040-4039(94)02311-X |
0.405 |
|
| 1995 |
Du Y, Kong F. Synthesis, conformation and glycosylation reaction of substituted 2,6-dioxabicyclo[3.1.1]heptanes:1,3-anhydro-2,4-di-O-benzyl-α-l-arabinopyranose Carbohydrate Research. 275: 259-273. DOI: 10.1016/0008-6215(95)00161-L |
0.378 |
|
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