Year |
Citation |
Score |
2024 |
Maji S, Ghotekar BK, Kulkarni SS. Total Synthesis of a Conjugation-Ready Tetrasaccharide Repeating Unit of O:3 O-antigen Polysaccharide. Organic Letters. PMID 38198674 DOI: 10.1021/acs.orglett.3c04225 |
0.355 |
|
2023 |
Rai D, Kulkarni SS. Total Synthesis of Conjugation-Ready Tetrasaccharide Repeating Units of a Multidrug-Resistant Pathogen Strain 34 and O5. Organic Letters. 25: 8332-8337. PMID 37955403 DOI: 10.1021/acs.orglett.3c03417 |
0.359 |
|
2023 |
Ghosh A, Kulkarni SS. Total Synthesis of a Linear Tetrasaccharide Repeating Unit of MO6-24. Organic Letters. 25: 7242-7246. PMID 37756139 DOI: 10.1021/acs.orglett.3c02872 |
0.351 |
|
2023 |
Paul A, Rai D, Pradhan K, Balhara P, Mishra AK, Kulkarni SS. Total Synthesis of a Structurally Complex Tetrasaccharide Repeating Unit of O43. Organic Letters. PMID 37603587 DOI: 10.1021/acs.orglett.3c02430 |
0.35 |
|
2023 |
Nalpe SS, Jana S, Kulkarni SS. Total Synthesis and Structure Confirmation of Fusaroside. The Journal of Organic Chemistry. PMID 37291052 DOI: 10.1021/acs.joc.3c00167 |
0.71 |
|
2023 |
Paul A, Kulkarni SS. Total Synthesis of the Repeating Units of 26 and TG155 via a Common Disaccharide. Organic Letters. PMID 37284758 DOI: 10.1021/acs.orglett.3c01618 |
0.309 |
|
2023 |
Shirsat AA, Rai D, Ghotekar BK, Kulkarni SS. Total Synthesis of Trisaccharide Repeating Unit of Strain M. Organic Letters. 25: 2913-2917. PMID 37052906 DOI: 10.1021/acs.orglett.3c00997 |
0.34 |
|
2023 |
Nalpe SS, Jana S, Kulkarni SS. Total Synthesis of a Trehalose-Containing Lipooligosaccharide Analogue from . Organic Letters. PMID 36867005 DOI: 10.1021/acs.orglett.3c00378 |
0.735 |
|
2023 |
Rai D, Kulkarni SS. Total Synthesis of Trisaccharide Repeating Unit of Type 8 (CP8) Capsular Polysaccharide. Organic Letters. 25: 1509-1513. PMID 36852946 DOI: 10.1021/acs.orglett.3c00290 |
0.388 |
|
2022 |
Luong P, Ghosh A, Moulton KD, Kulkarni SS, Dube DH. Synthesis and Application of Rare Deoxy Amino l-Sugar Analogues to Probe Glycans in Pathogenic Bacteria. Acs Infectious Diseases. 8: 889-900. PMID 35302355 DOI: 10.1021/acsinfecdis.2c00060 |
0.381 |
|
2021 |
Ghosh A, Kulkarni SS. Total Synthesis of the Repeating Unit of Zwitterionic Polysaccharide Sp1. The Journal of Organic Chemistry. PMID 34860529 DOI: 10.1021/acs.joc.1c02409 |
0.447 |
|
2021 |
Puri K, Kulkarni SS. Total Synthesis of the Phosphorylated Zwitterionic Trisaccharide Repeating Unit of 3240. Organic Letters. PMID 34459612 DOI: 10.1021/acs.orglett.1c02487 |
0.413 |
|
2021 |
Biswas S, Ghotekar BK, Kulkarni SS. Total Synthesis of the All-Rare Sugar-Containing Pentasaccharide Repeating Unit of the O-Polysaccharide of Strain 302-73 (Serotype O1). Organic Letters. PMID 34291950 DOI: 10.1021/acs.orglett.1c02239 |
0.487 |
|
2021 |
Paul A, Kulkarni SS. Synthesis of L-hexoses: an Update. Chemical Record (New York, N.Y.). PMID 34075685 DOI: 10.1002/tcr.202100087 |
0.377 |
|
2021 |
Rai D, Sanapala SR, Kulkarni SS. Serendipitous one-pot synthesis of chiral dienes from pyranosidic 2,4-bistriflates. Carbohydrate Research. 505: 108351. PMID 34044223 DOI: 10.1016/j.carres.2021.108351 |
0.813 |
|
2021 |
Pathan EK, Ghosh B, Podilapu AR, Kulkarni SS. Total Synthesis of the Repeating Unit of Zwitterionic Polysaccharide A1. The Journal of Organic Chemistry. PMID 33843231 DOI: 10.1021/acs.joc.0c02935 |
0.424 |
|
2021 |
Jana S, Sarpe VA, Kulkarni SS. Total Synthesis and Structure Revision of a Fungal Glycolipid Fusaroside. Organic Letters. 23: 1664-1668. PMID 33591200 DOI: 10.1021/acs.orglett.1c00077 |
0.804 |
|
2020 |
Williams DA, Pradhan K, Paul A, Olin IR, Tuck OT, Moulton KD, Kulkarni SS, Dube DH. Metabolic inhibitors of bacterial glycan biosynthesis. Chemical Science. 11: 1761-1774. PMID 34123271 DOI: 10.1039/c9sc05955e |
0.292 |
|
2020 |
Rai D, Kulkarni SS. Recent advances in β-l-rhamnosylation. Organic & Biomolecular Chemistry. 18: 3216-3228. PMID 32270840 DOI: 10.1039/d0ob00297f |
0.378 |
|
2020 |
Jana S, Kulkarni SS. Synthesis of trehalose glycolipids. Organic & Biomolecular Chemistry. 18: 2013-2037. PMID 32115587 DOI: 10.1039/d0ob00041h |
0.719 |
|
2020 |
Dadhich R, Mishra M, Ning S, Jana S, Sarpe VA, Mahato J, Duan M, Kulkarni SS, Kapoor S. A Virulence-associated glycolipid with distinct conformational attributes: Impact on lateral organization of host plasma membrane, autophagy and signaling. Acs Chemical Biology. PMID 32078292 DOI: 10.1021/Acschembio.9B00991 |
0.742 |
|
2020 |
Kulkarni SS, Ghosh B. Novel Protecting Groups for Oligosaccharides Synthesis. Chemistry, An Asian Journal. PMID 31895493 DOI: 10.1002/asia.201901621 |
0.356 |
|
2020 |
Ghotekar BK, Podilapu AR, Kulkarni SS. Total Synthesis of the Lipid-Anchor-Attached Core Trisaccharides of Lipoteichoic Acids of and Uo5. Organic Letters. 22: 537-541. PMID 31887057 DOI: 10.1021/acs.orglett.9b04264 |
0.474 |
|
2020 |
Behera A, Rai D, Kulkarni SS. Total Syntheses of Conjugation-Ready Trisaccharide Repeating Units of O11 and Type 5 Capsular Polysaccharide for Vaccine Development. Journal of the American Chemical Society. 142: 456-467. PMID 31815459 DOI: 10.1021/jacs.9b11309 |
0.404 |
|
2020 |
Williams DA, Pradhan K, Paul A, Olin IR, Tuck OT, Moulton KD, Kulkarni SS, Dube DH. Metabolic inhibitors of bacterial glycan biosynthesis Chemical Science. 11: 1761-1774. DOI: 10.1039/C9Sc05955E |
0.262 |
|
2020 |
Pradhan K, Kulkarni SS. Cover Feature: Synthesis of Nonulosonic Acids (Eur. J. Org. Chem. 44/2020) European Journal of Organic Chemistry. 2020: 6815-6815. DOI: 10.1002/EJOC.202001248 |
0.33 |
|
2020 |
Pradhan K, Kulkarni SS. Synthesis of Nonulosonic Acids European Journal of Organic Chemistry. 2020: 6819-6830. DOI: 10.1002/ejoc.202000250 |
0.353 |
|
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 |
0.728 |
|
2018 |
Emmadi M, Kulkarni SS. Synthesis of Rare Deoxy Amino Sugar Building Blocks Enabled the Total Synthesis of a Polysaccharide Repeating Unit Analogue from the LPS of Psychrobacter cryohalolentis K5. The Journal of Organic Chemistry. 83: 14323-14337. PMID 30388010 DOI: 10.1021/Acs.Joc.8B02037 |
0.791 |
|
2018 |
Jana S, Sarpe VA, Kulkarni SS. Total Synthesis of Emmyguyacins A and B, Potential Fusion Inhibitors of Influenza Virus. Organic Letters. PMID 30350678 DOI: 10.1021/Acs.Orglett.8B03073 |
0.778 |
|
2018 |
Behera A, Rai D, Kushwaha D, Kulkarni SS. Total Synthesis of Trisaccharide Repeating Unit of O-Specific Polysaccharide of Pseudomonas fluorescens BIM B-582. Organic Letters. PMID 30187759 DOI: 10.1021/acs.orglett.8b02669 |
0.51 |
|
2018 |
Behera A, Kulkarni SS. Chemical Synthesis of Rare, Deoxy-Amino Sugars Containing Bacterial Glycoconjugates as Potential Vaccine Candidates. Molecules (Basel, Switzerland). 23. PMID 30103434 DOI: 10.3390/molecules23081997 |
0.37 |
|
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 |
0.762 |
|
2018 |
Podilapu AR, Emmadi M, Kulkarni SS. Expeditious Synthesis of Ieodoglucomides A and B from the Marine‐Derived Bacterium Bacillus licheniformis European Journal of Organic Chemistry. 2018: 3230-3235. DOI: 10.1002/Ejoc.201800209 |
0.777 |
|
2017 |
Podilapu AR, Kulkarni SS. Total Synthesis of Repeating Unit of O-Polysaccharide of Providencia alcalifaciens O22 via One-Pot Glycosylation. Organic Letters. 19: 5466-5469. PMID 28949149 DOI: 10.1021/acs.orglett.7b02791 |
0.442 |
|
2017 |
Elharar Y, Podilapu AR, Guan Z, Kulkarni SS, Eichler J. Assembling glycan-charged dolichol phosphates: Chemoenzymatic synthesis of a Haloferax volcanii N-glycosylation pathway intermediate. Bioconjugate Chemistry. PMID 28809486 DOI: 10.1021/acs.bioconjchem.7b00436 |
0.314 |
|
2017 |
Jana S, Mondal S, Kulkarni SS. Chemical Synthesis of Biosurfactant Succinoyl Trehalose Lipids. Organic Letters. PMID 28328221 DOI: 10.1021/Acs.Orglett.7B00550 |
0.744 |
|
2016 |
Clark EL, Emmadi M, Krupp KL, Podilapu AR, Helble JD, Kulkarni SS, Dube DH. Development of rare bacterial monosaccharide analogs for metabolic glycan labeling in pathogenic bacteria. Acs Chemical Biology. PMID 27766829 DOI: 10.1021/Acschembio.6B00790 |
0.769 |
|
2016 |
Sanapala SR, Kulkarni SS. From l-Rhamnose to Rare 6-Deoxy-l-Hexoses. Organic Letters. PMID 27404897 DOI: 10.1021/acs.orglett.6b01796 |
0.796 |
|
2016 |
Chaube MA, Sarpe VA, Jana S, Kulkarni SS. First total synthesis of trehalose containing tetrasaccharides from Mycobacterium smegmatis. Organic & Biomolecular Chemistry. PMID 27035801 DOI: 10.1039/C6Ob00412A |
0.771 |
|
2016 |
Sanapala SR, Kulkarni SS. Expedient Route to Access Rare Deoxy Amino L-Sugar Building Blocks for the Assembly of Bacterial Glycoconjugates. Journal of the American Chemical Society. PMID 27002789 DOI: 10.1021/jacs.6b01823 |
0.817 |
|
2015 |
Sarpe VA, Jana S, Kulkarni SS. Synthesis of Mycobacterium tuberculosis Sulfolipid-3 Analogues and Total Synthesis of the Tetraacylated Trehaloglycolipid of Mycobacterium paraffinicum. Organic Letters. PMID 26652194 DOI: 10.1021/Acs.Orglett.5B03300 |
0.804 |
|
2015 |
Chaube MA, Kulkarni SS. First Total Synthesis of Trehalose-Containing Branched Oligosaccharide OSE-1 of Mycobacterium gordonae (Strain 990). Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 13544-8. PMID 26251305 DOI: 10.1002/chem.201502521 |
0.8 |
|
2015 |
Sanapala SR, Kulkarni SS. One-pot synthesis of bicyclic sugar oxazolidinone from d-glucosamine Rsc Advances. 5: 22426-22430. DOI: 10.1039/c5ra02270c |
0.376 |
|
2015 |
Jana S, Emmadi M, Kulkarni SS. First synthesis of the α- L-serine linked consensus disaccharide of neisseria gonorrhoeae and neisseria meningitidis Israel Journal of Chemistry. 55: 398-402. DOI: 10.1002/Ijch.201400152 |
0.815 |
|
2015 |
Sanapala SR, Kulkarni SS. ChemInform Abstract: One-Pot Synthesis of Bicyclic Sugar Oxazolidinone from D-Glucosamine. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201530250 |
0.419 |
|
2014 |
Sarpe VA, Kulkarni SS. Expeditious synthesis of Mycobacterium tuberculosis sulfolipids SL-1 and Ac2SGL analogues. Organic Letters. 16: 5732-5. PMID 25322198 DOI: 10.1021/ol5027987 |
0.813 |
|
2014 |
Podilapu AR, Kulkarni SS. First synthesis of Bacillus cereus Ch HF-PS cell wall trisaccharide repeating unit. Organic Letters. 16: 4336-9. PMID 25101800 DOI: 10.1021/ol5021527 |
0.412 |
|
2014 |
Emmadi M, Kulkarni SS. Total synthesis of the bacillosamine containing α-l-serine linked trisaccharide of Neisseria meningitidis. Carbohydrate Research. 399: 57-63. PMID 24853576 DOI: 10.1016/J.Carres.2014.04.011 |
0.823 |
|
2014 |
Emmadi M, Kulkarni SS. Recent advances in synthesis of bacterial rare sugar building blocks and their applications. Natural Product Reports. 31: 870-9. PMID 24700208 DOI: 10.1039/C4Np00003J |
0.803 |
|
2014 |
Sanapala SR, Kulkarni SS. Chemical synthesis of asparagine-linked archaeal N-glycan from Methanothermus fervidus. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 3578-83. PMID 24616211 DOI: 10.1002/chem.201304950 |
0.8 |
|
2014 |
Behera A, Emmadi M, Kulkarni SS. Total synthesis of MECA-79 Rsc Advances. 4: 58573-58580. DOI: 10.1039/C4Ra12631A |
0.809 |
|
2014 |
Adak S, Emmadi M, Kulkarni SS. Synthesis of the trisaccharide moiety and a cholesteryl analog of phyteumosides Rsc Advances. 4: 7611-7616. DOI: 10.1039/C3Ra47523A |
0.83 |
|
2013 |
Thota VN, Brahmaiah M, Kulkarni SS. Synthesis of a C-glycoside analogue of β-galactosyl ceramide, a potential HIV-1 entry inhibitor. The Journal of Organic Chemistry. 78: 12082-9. PMID 24199837 DOI: 10.1021/jo402115w |
0.338 |
|
2013 |
Emmadi M, Kulkarni SS. Synthesis of orthogonally protected bacterial, rare-sugar and D-glycosamine building blocks. Nature Protocols. 8: 1870-89. PMID 24008382 DOI: 10.1038/Nprot.2013.113 |
0.8 |
|
2013 |
Sarpe VA, Kulkarni SS. Desymmetrization of trehalose via regioselective DIBAL reductive ring opening of benzylidene and substituted benzylidene acetals. Organic & Biomolecular Chemistry. 11: 6460-5. PMID 23982734 DOI: 10.1039/c3ob41389f |
0.796 |
|
2013 |
Emmadi M, Kulkarni SS. Orthogonally protected D-galactosamine thioglycoside building blocks via highly regioselective, double serial and double parallel inversions of β-D-thiomannoside. Organic & Biomolecular Chemistry. 11: 4825-30. PMID 23774997 DOI: 10.1039/C3Ob40935J |
0.799 |
|
2013 |
Emmadi M, Kulkarni SS. Expeditious synthesis of bacterial, rare sugar building blocks to access the prokaryotic glycome. Organic & Biomolecular Chemistry. 11: 3098-102. PMID 23563627 DOI: 10.1039/C3Ob40615F |
0.821 |
|
2013 |
Yen YF, Kulkarni SS, Chang CW, Luo SY. Concise synthesis of α-galactosyl ceramide from D-galactosyl iodide and D-lyxose. Carbohydrate Research. 368: 35-9. PMID 23333444 DOI: 10.1016/j.carres.2012.11.008 |
0.423 |
|
2013 |
Sarpe VA, Kulkarni SS. ChemInform Abstract: Regioselective Protection and Functionalization of Trehalose Cheminform. 44: no-no. DOI: 10.1002/CHIN.201349240 |
0.297 |
|
2012 |
Thota VN, Gervay-Hague J, Kulkarni SS. Synthesis of β-C-galactosyl D- and L-alanines. Organic & Biomolecular Chemistry. 10: 8132-9. PMID 22961309 DOI: 10.1039/C2Ob26078F |
0.686 |
|
2012 |
Chaube MA, Kulkarni SS. ChemInform Abstract: Stereoselective Construction of 1,1-α,α-Glycosidic Bonds Cheminform. 43: no-no. DOI: 10.1002/CHIN.201241251 |
0.749 |
|
2011 |
Sarpe VA, Kulkarni SS. Synthesis of maradolipid. The Journal of Organic Chemistry. 76: 6866-70. PMID 21739985 DOI: 10.1021/jo200979n |
0.822 |
|
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 |
0.69 |
|
2011 |
Ho LT, Kulkarni SS, Lee JC. Development of sodium-dependent glucose co-transporter 2 inhibitors as potential anti-diabetic therapeutics. Current Topics in Medicinal Chemistry. 11: 1476-512. PMID 21510836 DOI: 10.2174/156802611795860915 |
0.222 |
|
2011 |
Emmadi M, Kulkarni SS. Rapid transformation of D-mannose into orthogonally protected D-glucosamine and D-galactosamine thioglycosides. The Journal of Organic Chemistry. 76: 4703-9. PMID 21510706 DOI: 10.1021/Jo200342V |
0.785 |
|
2010 |
Schombs M, Park FE, Du W, Kulkarni SS, Gervay-Hague J. One-pot syntheses of immunostimulatory glycolipids. The Journal of Organic Chemistry. 75: 4891-8. PMID 20387787 DOI: 10.1021/Jo100366V |
0.807 |
|
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 |
0.751 |
|
2009 |
Kulkarni SS, Gervay-Hague J. ChemInform Abstract: Synthesis of Glycolipid Antigens Cheminform. 40. DOI: 10.1002/CHIN.200935243 |
0.383 |
|
2008 |
Kulkarni SS, Gervay-Hague J. Two-step synthesis of the immunogenic bacterial glycolipid BbGL1. Organic Letters. 10: 4739-42. PMID 18798644 DOI: 10.1021/Ol801780C |
0.711 |
|
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 |
0.742 |
|
2008 |
Kulkarni SS, Gervay-Hague J. Synthesis of glycolipid antigens Acs Symposium Series. 990: 153-166. DOI: 10.1021/bk-2008-0990.ch007 |
0.711 |
|
2008 |
Shoda SI, Kulkarni SS, Gervay-Hague J. Glycoside Synthesis from Anomeric Halides Handbook of Chemical Glycosylation: Advances in Stereoselectivity and Therapeutic Relevance. 29-93. DOI: 10.1002/9783527621644.ch2 |
0.716 |
|
2007 |
Du W, Kulkarni SS, Gervay-Hague J. Efficient, one-pot syntheses of biologically active alpha-linked glycolipids. Chemical Communications (Cambridge, England). 2336-8. PMID 17844738 DOI: 10.1039/B702551C |
0.703 |
|
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 |
0.768 |
|
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 |
0.762 |
|
2006 |
Kulkarni SS, Gervay-Hague J. Efficient synthesis of a C-analogue of the immunogenic bacterial glycolipid BbGL2. Organic Letters. 8: 5765-8. PMID 17134267 DOI: 10.1021/Ol062354M |
0.656 |
|
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 |
0.756 |
|
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 |
0.751 |
|
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 |
0.708 |
|
2005 |
Kulkarni SS, Chi F, Hung S. Biologically Potent L-Hexoses and 6-Deoxy-L-hexoses: Syntheses and Applications Cheminform. 36. DOI: 10.1002/CHIN.200542277 |
0.332 |
|
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 |
0.786 |
|
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 |
0.758 |
|
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 |
0.781 |
|
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 |
0.753 |
|
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 |
0.741 |
|
2004 |
Kulkarni SS, Lee J, Hung S. Recent Advances in the Applications of D- and L-1,6-Anhydrohexopyranoses for the Synthesis of Oligosaccharides and Nature Products Cheminform. 35. DOI: 10.1002/CHIN.200435249 |
0.392 |
|
2004 |
Yang W, Lu X, Kulkarni SS, Hung S. Cu(OTf)2-Catalyzed Et3SiH-Reductive Etherification of Various Carbonyl Compounds with Trimethylsilyl Ethers. Cheminform. 35. DOI: 10.1002/CHIN.200404043 |
0.266 |
|
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 |
0.737 |
|
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 |
0.718 |
|
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