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2026
Synthesis of Conjugation-Ready Trisaccharide Repeating Units of Multidrug-Resistant Pathogen Acinetobacter baumannii MG1 and Strain 24
Aishwarya Shelke, Kartikey Singh, Suvarn S. Kulkarni* Org. Lett. 2026, 28, 16, 5207–5211 DOI
Total Synthesis of Conjugation‐Ready Tetrasaccharide Repeating Units of Pseudomonas Aeruginosa (Lányi) O11
Shirsat, A. A.; Chhabra, M.; Kulkarni, S. S. Asian J. 2026, 21 (3), e00950. DOI
Maji, S.; De, A. K.; Kulkarni, S. S. J. Sci. Food Agric. 2026. DOI
2025
Chemical Synthesis of Pseudomonas aeruginosa, Staphylococcus aureus, and Acinetobacter baumannii Capsular Polysaccharide Fragments as Leads for Cross-Protection
Mishra, A. K.; Reuber, E. E.; Rai, D.; Sander, L. E.; Duerr, J.; Graeber, S. Y.; Mall, M. A.; Fries, B. C.; Seeberger, P. H.; Kulkarni, S. S. Angew. Chem. Int. Ed. 2025. DOI
One-Pot Assembly of the Rare Sugar Containing Trisaccharide Repeating Unit of Pseudomonas putida TSh-18
Behera, S.; Patel, N.; Shelke, A.; Kulkarni, S. S. Org. Lett. 2025, 27 (50), 14023–14028. DOI
Toward Glycomimetic Immunomodulators: A Synthetic Dissection of Phocaeicola vulgatus Core Oligosaccharides and Their Recognition by DC-SIGN
Rai, D.; Nieto-Fabregat, F.; Dikshit, R.; Thépaut, M.; Fieschi, F.; Silipo, A.; Kulkarni, S. S. ACS Omega. 2025, 10 (43), 51985–52000. DOI
Examination of Acetylated Monosaccharides as Metabolic Probes in Bacteria
Sophia E. Nigrovic, Ankita Paul, Soumyakanta Maji, Antara Ghosh, Jack Tran, Phuong Luong, William J. Rackear, Elizabeth A. Stemmler, Karen D. Moulton, Suvarn S. Kulkarni*, Danielle H. Dube* ACS Infect. Dis. 2025, 11, 11, 3355–3363 DOI
Assessing O-Naphthylmethyl and O-Anthracenemethyl Glycosides as Metabolic Inhibitors of Bacterial Glycan Biosynthesis
Panhasith Ung, Ankita Paul, Soumyakanta Maji, Pilar Saavedra-Weis, Karen D. Moulton, Suvarn S. Kulkarni*, Danielle H. Dube* ACS Infect. Dis. 2025, ASAP DOI
Total Synthesis of the Conjugation-Ready Tetrasaccharide Repeating Unit of Multidrug-Resistant Pathogen Pseudomonas aeruginosa NCTC 8505 O-Antigen
Aishwarya Shelke, Kartikey Singh, Suvarn S. Kulkarni* Org. Lett. 2025, 27, 37, 10576–10581 DOI
Total synthesis of the trisaccharide repeating unit of the O-polysaccharide of Pragia fontium 97U124
Balasaheb K. Ghotekar , Suvarn S. Kulkarni* Carbohydrate Research 2025, 553, 109494. DOI
2024
Expanding the Scope of a One-Pot Double Displacement Protocol to Access the All-Rare-Sugar-Containing Trisaccharide Unit of Pseudomonas stutzeri OX1
Amar K. Mishra, Balasaheb K. Ghotekar, Chanchal K. Puley, Suvarn S. Kulkarni* Org. Lett. 2024, 26, 46, 9955–9960 DOI
Total synthesis of a structurally complex zwitterionic hexasaccharide repeating unit of polysaccharide B from Bacteroides fragilis via one-pot glycosylation
Krishna Puri, Suvarn S. Kulkarni* Commun. Chem. 2024, 7, 204. DOI
Total Synthesis of the Conjugation-Ready Tetrasaccharide Repeating Unit of Shewanella japonica Type Strain KMM 3299
Balasaheb K. Ghotekar, Suvarn S. Kulkarni*, Org. Lett., 2024, 26, 20, 4346–4350 DOI
Circumventing aglycon transfer en route to the synthesis of pentasaccharide thioglycoside donor for the chain extension of Plesiomonas shigelloides strain 302-73 (serotype O1) repeating unit
Balasaheb K. Ghotekar, Sayantan Biswas, Suvarn S. Kulkarni*, Carbohydr. Res. 2024, 537, 109073. DOI
Total Synthesis of Vibrio Cholerae O43 Tetrasaccharide Repeating Unit
Kabita Pradhan, Ankita Paul, Diksha Rai, Amar Kumar Mishra, Preeti Balhara, Suvarn S. Kulkarni* J. Org. Chem. 2024, 89, 6, 4019–4030 DOI
Atomic-Level Dissection of DC-SIGN Recognition of Bacteroides vulgatus LPS Epitopes
Ferran Nieto-Fabregat, Qian Zhu, Corinne Vivès, Yunqin Zhang. Angela Marseglia, Fabrizio Chiodo, Michel Thépaut, Diksha Rai, Suvarn S. Kulkarni, Flaviana Di Lorenzo, Antonio Molinaro, Roberta Marchetti, Franck Fieschi, Guozhi Xiao, Biao Yu*, Alba Silipo* JACS Au 2024, 4, 2, 697–712 DOI
Total Synthesis of a Conjugation-Ready Tetrasaccharide Repeating Unit of Vibrio cholerae O:3 O-antigen Polysaccharide
Soumyakanta Maji, Balasaheb K. Ghotekar, Suvarn S. Kulkarni*, Org. Lett. 2024, 26, 3, 745–750 DOI
Total Synthesis of Conjugation-Ready Tetrasaccharide Repeating Units of a Multidrug-Resistant Pathogen Acinetobacter baumannii Strain 34 and O5
Diksha RaiSuvarn S. Kulkarni*, Org. Lett. 2023, 25, 46, 8332–8337 DOI
2023
Total Synthesis of a Linear Tetrasaccharide Repeating Unit of Vibrio vulnificus MO6-24
Antara Ghosh, Suvarn S. Kulkarni*, Org. Lett. 2023, 25, 39, 7242–7246 DOI
Thioglycosides Act as Metabolic Inhibitors of Bacterial Glycan Biosynthesis
Isabella de la Luz Quintana, Ankita Paul, Aniqa Chowdhury, Karen D. Moulton, Suvarn S. Kulkarni*, Danielle H. Dube*, ACS Infect. Dis. 2023, 9, 10, 2025–2035 DOI
Total Synthesis of a Structurally Complex Tetrasaccharide Repeating Unit of Vibrio cholerae O43
Ankita Paul, Diksha Rai, Kabita Pradhan, Preeti Balhara, Amar Kumar Mishra, Suvarn S. Kulkarni*, Org. Lett. 2023, 25, 34, 6413–6418 DOI
Total Synthesis and Structure Confirmation of Fusaroside
Sudhakar S. Nalpe, Santanu Jana, Suvarn S. Kulkarni*, J. Org. Chem. 2023, 88, 13, 8175–8178 DOI
Total Synthesis of the Repeating Units of Proteus penneri 26 and Proteus vulgaris TG155 via a Common Disaccharide
Ankita Paul, Suvarn S. Kulkarni*, Org. Lett. 2023, 25, 23, 4400–4405 DOI
Total Synthesis of Trisaccharide Repeating Unit of Staphylococcus aureus Strain M
Archana A. Shirsat, Diksha Rai, Balasaheb K. Ghotekar, Suvarn S. Kulkarni*, Org. Lett. 2023, 25, 16, 2913–2917 DOI
Total Synthesis of a Trehalose-Containing Lipooligosaccharide Analogue from Mycobacterium linda
Sudhakar S. Nalpe, Santanu Jana, Suvarn S. Kulkarni*, Org. Lett. 2023, 25, 10, 1717–1721 DOI
Total Synthesis of Trisaccharide Repeating Unit of Staphylococcus aureus Type 8 (CP8) Capsular Polysaccharide
Diksha Rai, Suvarn S. Kulkarni*, Org. Lett. 2023, 25, 9, 1509–1513 DOI
2022
Polysaccharide corona: The acetyl-rich envelope wraps the extracellular membrane vesicles and the cells of Shewanella vesiculosa providing adhesiveness
Angela Casilloa, Rossella Di Guidaa, Domenico Cavassoa, Antonietta Stellavatob, Diksha Raic, Fumiaki Yokoyamad, Kouhei Kamasakad, Jun Kawamotod, Tatsuo Kuriharad, Chiara Schiraldib, Suvarn Kulkarnic, Luigi Paduanoa, Maria Michela Corsaroa,*, Carbohydrate Polymers , 2022,297, 120036. DOI
Small Carbohydrate Derivatives as Potent Antibiofilm Agents
Kartikey Singh, Suvarn S. Kulkarni*, J. Med. Chem., 2022,65, 13, 8525-8549. DOI
Total Synthesis of the Repeating Units of O-Specific Polysaccharide of Pseudomonas chlororaphis subsp. aureofaciens UCM B-306 via One-Pot Glycosylation
Bhaswati Ghosh, Nabarupa Bhattacharjee, Ananda Rao Podilapu, Krishna Puri, Suvarn S. Kulkarni*, Org. Lett., 2022,24, 20, 3696-3701. DOI
Synthesis and Application of Rare Deoxy Amino L-Sugar Analogs to Probe Glycans in Pathogenic Bacteria.
Phuong Luong1#, Antara Ghosh2#, Karen D. Moulton1, Suvarn S. Kulkarni2*, and Danielle H. Dube1* , ACS Infect. Dis., 2022, 8, 4, 889–900. DOI
2021
Total Synthesis of the Repeating Unit of Streptococcus pneumoniae Zwitterionic Polysaccharide Sp1
Antara Ghosh, Suvarn S. Kulkarni* , J. Org. Chem. 2021, 86, 24, 18292–18299 . DOI
Synthesis of L-Hexoses: An Update
Ankita Paul, Suvarn S Kulkarni* , Chem. Rec., 2021, 21, 1-15. DOI
Total Synthesis of the Phosphorylated Zwitterionic Trisaccharide Repeating Unit of Photorhabdus temperata cinerea 3240.
Krishna Puri, Suvarn S. Kulkarni* , Org. Lett. 2021, 23, 18, 7083–7087. DOI
Total Synthesis of the All-Rare Sugar-Containing Pentasaccharide Repeating Unit of the O-Polysaccharide of Plesiomonas shigelloides Strain 302-73 (Serotype O1)
Sayantan Biswas, Balasaheb K. Ghotekar, Suvarn S. Kulkarni* , Org. Lett. 2021, 23, 15, 6137–6142. DOI
Serendipitous one-pot synthesis of chiral dienes from pyranosidic 2,4-bistriflates
Diksha Rai, Someswara Rao Sanapala, Suvarn S. Kulkarni, Carbohydr. Res. 2021, 505, 108351, 0008-6215. DOI
Total Synthesis of the Repeating Unit of Bacteroides fragilis Zwitterionic Polysaccharide A1
Ennus K. Pathan, Bhaswati Ghosh, Ananda Rao Podilapu, Suvarn S. Kulkarni*, J. Org. Chem. 2021, 86, 9, 6090–6099. DOI
Total Synthesis and Structure Revision of a Fungal Glycolipid Fusaroside
Total Synthesis and Structure Revision of a Fungal Glycolipid Fusaroside
Santanu Jana, Vikram A. Sarpe, Suvarn S. Kulkarni*, Org. Lett. 2021, 23, 5, 1664–1668. DOI
2020
Synthesis of Nonulosonic Acids
Synthesis of Nonulosonic Acids
Kabita Pradhan, Suvarn S. Kulkarni, Eur. J. Org. Chem., 2020,6819-6830.
Recent advances in β-L-rhamnosylation
Recent advances in β-L-rhamnosylation
Rai, D.; Kulkarni, S. S, Org. Biomol. Chem., 2020, 18, 3216-3228.
Metabolic inhibitors of bacterial glycan biosynthesis
Metabolic inhibitors of bacterial glycan biosynthesis
D. A. Williams, K. Pradhan, A. Paul, I. R. Olin, O. T. Tuck, K. D. Moulton, S. S. Kulkarni and D. H. Dube, Chem. Sci., 2020,11, 1761-1774.
Synthesis of trehalose glycolipids
Synthesis of trehalose glycolipids
Santanu Jana and Suvarn S. Kulkarni, Org. Biomol. Chem., 2020,18, 2013-2037.
Total Synthesis of the Lipid-Anchor-Attached Core Trisaccharides of Lipoteichoic Acids of Streptococcus pneumoniae and Streptococcus oralis Uo5
Balasaheb K. Ghotekar, Ananda Rao Podilapu, Suvarn S. Kulkarni* , Org. Lett. 2020, 22, 2, 537–541.
Total Syntheses of Conjugation-Ready Trisaccharide Repeating Units of Pseudomonas aeruginosa O11 and Staphylococcus aureus Type 5 Capsular Polysaccharide for Vaccine Development
Archanamayee Behera, Diksha Rai, Suvarn, S. Kulkarni* , J. Am. Chem. Soc. 2020, 142, 1, 456–467.
Advances in Protecting Groups for Oligosaccharide Synthesis
Bhaswati Ghosh and Suvarn S. Kulkarni, Chem. Asian J. 2020, 15, 450.
2018
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
Madhu Emmadi, Suvarn S. Kulkarni*, J. Org. Chem. 2018, 83, 23, 14323–14337. DOI
Total Synthesis of Emmyguyacins A and B, Potential Fusion Inhibitors of Influenza Virus
Santanu Jana, Vikram A. Sarpe, Suvarn S. Kulkarni*, Org. Lett. 2018, 20, 21, 6938–6942. DOI
Total Synthesis of Trisaccharide Repeating Unit of O-Specific Polysaccharide of Pseudomonas fluorescens BIM B-582
Archanamayee Behera, Diksha Rai, Divya Kushwaha, Suvarn S. Kulkarni*, Org. Lett. 2018, 20, 18, 5956–5959. DOI
Chemical Synthesis of Rare, Deoxy-Amino Sugars Containing Bacterial Glycoconjugates as Potential Vaccine Candidates
Archanamayee Behera and Suvarn S. Kulkarni*, Molecules. 2018, 23, 1997. DOI
Expeditious Synthesis of Ieodoglucomides A and B from the Marine-Derived Bacterium Bacillus licheniformis
Ananda Rao Podilapu, Madhu Emmadi, Suvarn S. Kulkarni, Eur.J.Org.Chem. 2018, 3230-3235. DOI
“One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates
Suvarn S. Kulkarni*, Cheng-Chung Wang*, Narayana Murthy Sabbavarapu, Ananda Rao Podilapu, Pin-Hsuan Liao, Shang-Cheng Hung*, Chem. Rev. 2018, 118, 17, 8025–8104. DOI
2017
Total Synthesis of Repeating Unit of O-Polysaccharide of Providencia alcalifaciens O22 via One-Pot Glycosylation
Ananda Rao Podilapu and Suvarn S. Kulkarni*, Org. Lett. 2017, 19, 5466-5469. DOI
Assembling Glycan-Charged Dolichol Phosphates: Chemoenzymatic Synthesis of a Haloferax volcanii N-Glycosylation Pathway Intermediate
Yifat Elharar, Ananda Rao Podilapu, Ziqiang Guan, Suvarn S. Kulkarni*, Jerry Eichler*, Bioconjugate Chem. 2017, 28, 9, 2461–2470. DOI
Chemical Synthesis of Biosurfactant Succinoyl Trehalose Lipids
Santanu Jana, Sumana Mondal, Suvarn S. Kulkarni*, Org. Lett. 2017, 19, 7, 1784–1787. DOI
2016
Development of Rare Bacterial Monosaccharide Analogs for Metabolic Glycan Labeling in Pathogenic Bacteria
Clark, E. L.; Emmadi, M.; Krupp, K. L.; Podilapu, A. R.; Helble, J. D.; Kulkarni, S. S.; Dube, D. H., ACS Chem. Biol. 2016, 11, 3365-3373. DOI
From l-Rhamnose to Rare 6-Deoxy-l-Hexoses
Someswara Rao Sanapala, Suvarn S. Kulkarni*, Org. Lett. 2016, 18, 15, 3790–3793. DOI
Expedient Route To Access Rare Deoxy Amino l-Sugar Building Blocks for the Assembly of Bacterial Glycoconjugates
Someswara Rao Sanapala, Suvarn S. Kulkarni*, J. Am. Chem. Soc. 2016, 138, 14, 4938–4947. DOI
Synthesis of Mycobacterium tuberculosis Sulfolipid-3 Analogues and Total Synthesis of the Tetraacylated Trehaloglycolipid of Mycobacterium paraffinicum
Vikram A. Sarpe, Santanu Jana, Suvarn S. Kulkarni*, Org. Lett. 2016, 18, 1, 76–79 DOI
First total synthesis of trehalose containing tetrasaccharides from Mycobacterium smegmatis
Manishkumar A. Chaube, Vikram A. Sarpe, Santanu Janaa and Suvarn S. Kulkarni*, Org. Biomol. Chem., 2016,14, 5595-5598. DOI
2015
First Total Synthesis of Trehalose-Containing Branched Oligosaccharide OSE-1 of Mycobacterium gordonae (Strain 990)
Manishkumar A. Chaube and Suvarn S. Kulkarni*, Chemistry – A European Journal. 2015, 21 (39) 13465-13819. DOI
First Synthesis of the α-L-Serine Linked Consensus Disaccharide of Neisseria gonorrhoeae and Neisseria meningitidis
Santanu Jana, Madhu Emmadi, Suvarn S. Kulkarni, Israel Journal of Chemistry. 2015, 55 (3‐4), 398-402. DOI
One-pot synthesis of bicyclic sugar oxazolidinone from D-glucosamine
Sanapala, S. R.; Kulkarni, S. S. RSC Adv. 2015, 5 (29), 22426–22430. DOI
2014
Total synthesis of the bacillosamine containing α-l-serine linked trisaccharide of Neisseria meningitidis
Emmadi, M.; Kulkarni, S. S. Carbohydr. Res. 2014, 399, 57–63. DOI
Expeditious Synthesis of Mycobacterium tuberculosis Sulfolipids SL-1 and Ac2SGL Analogues
Sarpe, V. A.; Kulkarni, S. S. Org. Lett. 2014, 16 (21), 5732–5735. DOI
First Synthesis of Bacillus cereus Ch HF-PS Cell Wall Trisaccharide Repeating Unit
Podilapu, A. R.; Kulkarni, S. S. Org. Lett. 2014, 16 (16), 4336–4339. DOI
Chemical Synthesis of Asparagine‐Linked Archaeal N‐Glycan from Methanothermus fervidus
Sanapala, S. R.; Kulkarni, S. S. Chem. Eur. J. 2014, 20, 3578–3583. DOI
Total synthesis of MECA-79
Behera, A.; Emmadi, M.; Kulkarni, S. S. RSC Adv. 2014, 4 (102), 58573–58580. DOI
Synthesis of the trisaccharide moiety and a cholesteryl analog of phyteumosides
Adak, S.; Emmadi, M.; Kulkarni, S. S. RSC Adv. 2014, 4 (15), 7611–7616. DOI
Recent advances in synthesis of bacterial rare sugar building blocks and their applications
Emmadi, M.; Kulkarni, S. S. Nat. Prod. Rep. 2014, 31 (7), 870–879. DOI
2013
Synthesis of a C-Glycoside Analogue of β-Galactosyl Ceramide, a Potential HIV-1 Entry Inhibitor
Thota, V. N.; Brahmaiah, M.; Kulkarni, S. S. J. Org. Chem. 2013, 78 (23), 12082–12089. DOI
Synthesis of orthogonally protected bacterial, rare-sugar and D-glycosamine building blocks
Emmadi, M.; Kulkarni, S. S. Nat. Protoc. 2013, 8, 1870–1889. DOI
Concise synthesis of α-galactosyl ceramide from d-galactosyl iodide and d-lyxose
Yen, Y. F.; Kulkarni, S. S.; Chang, C. W.; Luo, S. Y. Carbohydr. Res. 2013, 368, 35–39. DOI
Desymmetrization of trehalose via regioselective DIBAL reductive ring opening of benzylidene and substituted benzylidene acetals
Sarpe, V. A.; Kulkarni, S. S. Org. Biomol. Chem. 2013, 11, 6460–6465. DOI
Orthogonally protected d-galactosamine thioglycoside building blocks via highly regioselective, double serial and double parallel inversions of β-d-thiomannoside
Emmadi, M.; Kulkarni, S. S. Org. Biomol. Chem. 2013, 11, 4825–4830. DOI
Expeditious synthesis of bacterial, rare sugar building blocks to access the prokaryotic glycome
Emmadi, M.; Kulkarni, S. S. Org. Biomol. Chem. 2013, 11 (19), 3098–3102. DOI
2012
Synthesis of β-C-galactosyl D- and L-alanines
Thota, V. N.; Gervay-Hague, J.; Kulkarni, S. S. Org. Biomol. Chem. 2012, 10, 8132–8139. DOI
2011
Synthesis of β-C-galactosyl D- and L-alanines
Sarpe, V. A.; Kulkarni, S. S. J. Org. Chem. 2011, 76 (16), 6866–6870. DOI
Rapid Transformation of d-Mannose into Orthogonally Protected d-Glucosamine and d-Galactosamine Thioglycosides
Emmadi, M.; Kulkarni, S. S. J. Org. Chem. 2011, 76 (11), 4703–4709. DOI
2010
One-Pot Syntheses of Immunostimulatory Glycolipids
Schombs, M.; Park, F. E.; Du, W.; Kulkarni, S. S.; Gervay-Hague, J. J. Org. Chem. 2010, 75 (15), 4891–4898. DOI
2009
Synthesis of Alginate Oligosaccharides Containing L-Guluronic Acids
Chi, F.-C.; Kulkarni, S. S.; Zulueta, M.; Hung, S.-C. Chem. Asian J. 2009, 4, 386–390. DOI
2008
Two-Step Synthesis of the Immunogenic Bacterial Glycolipid BbGL1
Kulkarni, S. S.; Gervay-Hague, J. Org. Lett. 2008, 10 (21), 4739–4742. DOI
Regioselective one-pot protection of glucose
Wang, C.-C.; Kulkarni, S. S.; Lee, J.-C.; Luo, S.-Y.; Hung, S.-C. Nat. Protoc. 2008, 3, 97–113. DOI
2007
Regioselective one-pot protection of carbohydrates
Wang, C.-C.; Lee, J.-C.; Luo, S.-Y.; Kulkarni, S. S.; Huang, Y.-W.; Lee, C.-C.; Chang, K.-L.; Hung, S.-C. Nature 2007, 446, 896–899. DOI
Efficient, one-pot syntheses of biologically active α-linked glycolipids
Du, W.; Kulkarni, S. S.; Gervay-Hague, J. Chem. Commun. 2007, 2336–2338. DOI
Synthesis of 48 Disaccharide Building Blocks for the Assembly of a Heparin and Heparan Sulfate Oligosaccharide Library
Lu, L.-D.; Shie, C.-R.; Kulkarni, S. S.; Pan, G.-R.; Lu, X.-A.; Hung, S.-C. Org. Lett. 2006, 8 (26), 5995–5998. DOI
2006
Efficient Synthesis of a C-Analogue of the Immunogenic Bacterial Glycolipid BbGL2
Kulkarni, S. S.; Gervay-Hague, J. Org. Lett. 2006, 8 (25), 5765–5768. DOI
2-Allyloxyphenyl glycoside as a new and stable type of glycosyl donors
Lee, J.-C.; Pan, G.-R.; Kulkarni, S. S.; Luo, S.-Y.; Liao, C.-C.; Hung, S.-C. Tetrahedron Lett. 2006, 47 (10), 1621–1624. DOI
A Concise Synthesis of Tetrahydroxy-LCB, α-Galactosyl Ceramide, and 1,4-Dideoxy-1,4-imino-l-ribitol via d-Allosamines as Key Building Blocks
Luo, S.-Y.; Kulkarni, S. S.; Chou, C.-H.; Liao, W.-M.; Hung, S.-C. J. Org. Chem. 2006, 71 (3), 1226–1229. DOI
2005
Neighboring Group Participation of 9-Anthracenylmethyl Group in Glycosylation: Preparation of Unusual C-Glycosides
Kulkarni, S. S.; Liu, Y.-H.; Hung, S.-C. J. Org. Chem. 2005, 70 (7), 2808–2811. DOI
Highlights in Organic Chemistry (Metal Trifluoromethanesulfonates as Versatile Catalysts in Carbohydrate Synthesis)
Kulkarni, S. S.; Hung, S.-C. Lett. Org. Chem. 2005, 2 (8), 670–677. DOI
Cu(OTf)2 as an efficient and dual-purpose catalyst in the regioselective reductive ring opening of benzylidene acetals
Shie, C.-R.; Tzeng, Z.-H.; Kulkarni, S. S.; Uang, B.-J.; Hsu, C.-Y.; Hung, S.-C. Angew. Chem. Int. Ed. 2005, 44 (11), 1665–1668. DOI
2004
Biologically Potent L‐Hexoses and 6‐Deoxy‐L‐Hexoses: Their Syntheses and Applications
Kulkarni, S. S.; Chi, F.-C.; Hung, S.-C. J. Chin. Chem. Soc. 2004, 51 (5B), 1193–1200. DOI
Synthesis of Heparin Oligosaccharides
Lee, J.-C.; Lu, X.-A.; Kulkarni, S. S.; Wen, Y.-S.; Hung, S.-C. J. Am. Chem. Soc. 2004, 126 (2), 476–477. DOI
Regioselective Glycosylation of Neamine Core: A Facile Entry to Kanamycin B Related Analogues
Chou, C.-H.; Wu, C.-S.; Chen, C.-H.; Lu, L.-D.; Kulkarni, S. S.; Wong, C.-H.; Hung, S.-C. Org. Lett. 2004, 6 (4), 585–588. DOI
From D-Glucose to Biologically Potent L-Hexose Derivatives: Synthesis of α-L-Iduronidase Fluorogenic Detector and the Disaccharide Moieties of Bleomycin A2 and Heparan Sulfate
Lee, J.-C.; Chang, S.-W.; Liao, C.-C.; Chi, F.-C.; Chen, C.-S.; Wen, Y.-S.; Wang, C.-C.; Kulkarni, S. S.; Puranik, R.; Liu, Y.-H.; Hung, S.-C. Chem. Eur. J. 2004, 10, 399–415. DOI
2003
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
Tai, C.-A.; Kulkarni, S. S.; Hung, S.-C. J. Org. Chem. 2003, 68 (22), 8719–8722. DOI
Cu (OTf) 2-catalyzed Et3SiH-reductive etherification of various carbonyl compounds with trimethylsilyl ethers
Yang, W.-C.; Lu, X.-A.; Kulkarni, S. S.; Hung, S.-C. Tetrahedron Lett. 2003, 44 (42), 7837–7840. DOI
PATENTS
One pot synthesis of unprotected alpha/beta-O-glycolipids, Gervay-Hague J.; Du, W.; Kulkarni, S. S.; Schombs, M. PCT Int. Appl.(2008), WO 2008124729 A1 20081016
Method for preparing hexose derivatives, Hung, S.-C.; Wang, C.-C.; Lee, J.-C.; Luo, S.-Y.; Kulkarni, S. S.; Huang, Y. W.; Lee, C. C.; Chang, K. L., PCT Int. Appl. Publication No. US 7985856 B2 published on 26-Jul-2011 Application No. US 11/874697 filed on 18-Oct-2007.
BOOK CHAPTER
Synthesis of Hemagglutinin-Binding Trisaccharides, Wang, C.-C.; Kulkarni , S. S.; Zulueta, M. M. L.; Hung, S.-C. In 'The Molecular Immunology of Complex Carbohydrates-3, Advances in Experimental Medicine and Biology 705, Springer Science+Business Media, LLC, 2011, Chapter 37, pp 691-726.
Glycosyl chlorides, bromides and iodides, Kulkarni, S.S. and Gervay-Hague, J. Handbook of Chemical Glycosylation: Advances in Stereoselectivity and Therapeutic Relevance, Demchenko, A. V. Eds., Wiley-VCH, 2008, pp59-93.
Synthesis of glycolipid antigens, Kulkarni, S.S, and Gervay-Hague, J. In Chemical Glycobiology, Eds. Chen, X.; Halcomb, R.; Wang, P. G., ACS Symposium series 2008, 990, pp153-166.
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