Post Docs

Dr. Niklas Henrik Fischer

Dr. Yuxuan Hou

PhD Students

Natasha Videcrantz Faurschou; nvf@chem.ku.dk

Asger Røikjær Koue; asger@chem.ku.dk

Andreas Ketilsø Dam: akd@chem.ku.dk

Arminas Jurys: aj@chem.ku.dk

Niels Guldager: ng@chem.ku.dk

Tzu-Chun Lin: tcl@chem.ku.dk

Master Students

Amy Rose Lowans

Simon Risegaard

Jens Meisler Nielsen

Jonas Thygesen Larsen

Christine Sofie Haukohl J Schalck

Bachelor / Project students

Halfdan Naundrup Jepsen

Visiting Scholars / Temporary Staff

Victor Friis

Alicja Bałuta 

Alumni

Monya Harouel (Project 2012)

Maxime Douarre (Project 2013)

Valentin Rault (Project 2013 / 2016)

Camille Favre (Project 2013)

Guillaume Fanchon (Project 2013)

Elodie Perennes (Project 2014)

Maxime Pulcini (Project 2014)

Pernille S. Bols (Bachelor 2014)

Maria A. Bosi (Project 2015)

Anna G. Lund (Project 2015)

Megha Arya (Visitor 2016)

Eirikur T. Baldursson (Master 2016)

Dasol Hwang (Master 2016)

Hidde Elferink (visitor 2016)

Jun Miyatake Ondozabal (Master 2017 with Haldor Topsøe A/S)

Arminas Jurys (Visitor 2017)

Ignacio Álvarez (Master 2018)

Markus Häner (Visitor 2017-2018)

Muhan Zhao (Visitor 2017-2018)

Bolette Stougaard (Master 2018)

Christian Hammelev (Master 2018)

Julie M. Korsmeyer (Visitor 2018)

Martin Jæger Pedersen (PD 2016-2018)

Daniel Raydan (Master 2018-2019)

Jaime Moyano Villameriel (Master 2018-2019)

Simone Hilt Bartholin (Bachelor 2019)

Thomas Olsen (Bachelor 2019)

Nikolaj Agertoft Lundquist (Bachelor 2019)

Patricja Mala (visiting PhD student 2018/2019)

Kitt E. Østerlid (master student 2019-2020)

Allesandro Pinna (Ph.D. student 2020)

Nikolai B. Akselvoll (bachelor student 2020)

Benedicte Rønne Kristensen (bachelor 2020)

Cecilie Høgfeldt Jessen (bachelor 2020)

Emilie Lundquist Madsen (Project 2020)

Marius Haugstad (Project)

Josephine Fisker (Bachelor 2021)

Søren Peder Christensen (Project)

Thomas Holmstrøm (PhD 2021)

Michael Martin Nielsen (PhD 2021)

Frederik Bjerre (MSc 2021)

Thomas Olsen (MSc 2021)

Nikolaj Agertoft Lundquist (MSc 2021)

Yang Liang (杨 亮) (PhD 2022)

Nienke Julie Dekker (MSc 2022)

Morten Lang Zimmermann (MSc 2022)

Benedicte Rønne Kristensen (MSc 2022)

Andreas Ketils Dam (Bachelor 2022)

Khalid Ileye (Bachelor 2022)

Amy Rose Lowans (Project 2023)

Christine Sofie Haukohl J Schalck (Bachelor 2023)

Jonas Thygesen Larsen (Bachelor 2023)

Jesper Lund Christensen (Bachelor 2023)

Simon Risegaard (Bachelor 2023)

Oliver Blomquist (Bachelor 2023)

Neeraja C. Sajeev (Master 2023)

Vojtech Kunz (Master 2023)

Dr. Xifu Liang (PD 2023)

Dr. Martin Jæger Pedersen (PD 2020-23)

Catalina L. Bigalke (MSc 2024)

Nikolai Bjørn Akselvoll  (MSc 2024)

Daniel M. Feldballe (Bachelor 2024)

Anton K. Lawerentz  (Bachelor 2024)

Sofie I. H. Skov (Bachelor 2024)

Lærke B. Bødtcher (Bachelor 2024)

1. “Ring system-based conformational switches and their applications in sensing and liposomal drug delivery” H. Su, C.M. Pedersen SYNTHESIS 2022 (accepted)
2. “Vessel effects in organic chemical reactions; a century-old, overlooked phenomenon” M.M. Nielsen, M. Pedersen* Chem. Sci. 2022, 13, 6181-6196
3. “Catalytic conversion of d-glucose into lactic acid with Ba(OH)2 as a base catalyst:mechanistic insight by NMR techniques” Y. Zhao, R. Liu, M. Pedersen, Z. Zhang, Z. Guo, H. Chang, Y. Qiao, Y. Wang Mol. Liquids 2022, accepted
4. “NMR Diffusion Analysis of Catalytic Conversion Mixtures from Lignocellulose Biomass Using PSYCHE-iDOSY” Q. Zhao, M Pedersen, J. Wang; R. Liu, Y. Zhang, X. Yan, Z. Zhang, X. Hou, Y. Wang Green Energy & Enviroment 2022 (in press, online)
5. “Lupeol and pristimerin do not inhibit activation of the human sperm CatSper Ca(2+)-channel” A. Rehfeld, M. Pedersen F1000Research 2022 (accepted - online)
6. “Slow glycosylations: Activation of trichloroacetimidates under mild conditions using lithium salts and the role of counterions” N. Korber, M. Pedersen* Carbohydr. Res. 2022, (On-line)
7. “Stereoselective O-Glycosylations by Pyrylium Salt Organocatalysis” M.M. Nielsen, T. Holmstrøm, M. Pedersen* Angew. Chem. Int. Ed. 2022 (Accepted – Hot Paper)
8. “Silylated Sugars – Synthesis and Properties” M. Bols, T.G. Frihed, M.J. Pedersen, M. Pedersen* SYNLETT 2022, 33, 415-428
9. “Interactions between PAMAM-NH2 and 6-mercaptopurine: qualitative and quantitative NMR studies” Asian J. 2021, 16, 3658-3663
10. “Self-Promoted Glycosylation for the Synthesis of β-N-Glycosyl Sulfonyl Amides” P. Mala, M. Pedersen* Eur. J. Org. Chem. 2021, 5685-5689
11. “Protecting Carbohydrates with Ethers, Acetals and Orthoesters under Basic Conditions” L. Yang, M. Pedersen* Org. Biol. Chem. 2021, 19, 7598-7601
12. “Characterization of the acidity and basicity of green solvents by NMR techniques” K. Shi, M. Pedersen, H. Chang, J. Shi, Y. Wang, Y. Qiao Mag. Res. Lett. 2021 (https://doi.org/10.1016/j.mrl.2021.100001)
13. "Self-Promoted Stereoselective Glycosylations – Past, Present, Future" N.V. Faurschou,M. Pedersen* The Chem. Rec. , 2021, 21, 3063-3075
14. “d-Glucose Isomerization with PAMAM Dendrimers as Environmentally Friendly Catalysts” Z. Guo, M. Pedersen, P. Wang, M. Ma, Y. Zhao, Y. Qiao, Y. Wang J. Agric. Food Chem. 2021, 69, 17, 5105-5112
15. “Utilizing 3D DOSY NMR in the characterization of organic compounds in coal chemical wastewater” H. Ma, M. Pedersen, Q. Zhao, S. Jia, B. Yuan, X. Hou, Y. Wang Magn. Reson. Lett. 2021 (https://doi.org/10.1016/j.mrl.2021.100021)
16. "Pure shift NMR: Application of 1D PSYCHE and 1D TOCSY-PSYCHE Techniques for Directly Analyzing the Mixtures from Biomass-derived Platform Compound Hydrogenation/hydrogenolysis" Q. Zhao, H: Ma, M. Pedersen, M. Dou, Y. Qiao, X. Hou, Y. Qi, Y. Wang ACS Sus. Chem. Ing. 2021 9, 2456-2464
17. “Reactivity, Selectivity and Synthesis of 4-C-Silylated Glycosyl Donors and 4-Deoxy Analogues” M.J. Pedersen, M. Pedersen* Angew. Chem. Int. Ed. 2021 60 2689-2693
18. “Carbohydrate Derived Metal Chelator-Triggered Lipids for Liposomal Drug Delivery” T. Holmstrøm, M. G. Malle, S. Wu, K.J. Jensen, N.S. Hatzakis, M. Pedersen* Chem. Eur. J. 2021, 27, 6017-6922 (in-side cover)
19. "Easy access to a carbohydrate-based template for stimuli-responsive surfactants" T. Holmstrøm, D Raydan, M. Pedersen* Beilstein J. Org. Chem. 2020 16, 2788-2794
20. “Conformational lock of glycosyl donors using cyclic carbamates.” J.M. Villameriel, M. Pedersen* Eur. JOC 2020, 41, 6459-6467
21. “Synthesis and Glycosylation Properties of C6-silylated Ido- and Gluco-pyranosyl donors” I. Álvarez, M. Pedersen* Eur JOC, 2020, 4621-4634
22. “Enzyme Catalyzed Regioselective Acetylation of Functionalized Glycosides” T. Holmstrøm, M. Pedersen* Eur. JOC 2020, 4612-4615
23. "Chemoselectivity in Self-Promoted Glycosylation: N- versus O-Glycosylation." VIP paper Pinna, C. M. Pedersen* Eur. JOC 2020, 3914-3917
24. “Ternary deep eutectic solvents catalyzed d-glucosamine self-condensation to

deoxyfructosazine: NMR study” P. Liu, C.M. Pedersen, J. Zhang, R. Liu, Z. Zhang, X. Hou, Y. Wang Green Energy & Environment, 2020, https://doi.org/10.1016/j.gee.2020.04.010.

25. “Catalytic and Atom Economic Glycosylation using Glycosyl Formates and Cheap Metal Salts.” L. Yang, C.H. Hammelev, M. Pedersen* CHEMSUSCHEM 2020, 13, 3166-3171
26. “Scalable Synthesis of Hydroxymethyl alkylfuranoates as Stable 2,5-Furandicarboxylic acid Precursors” M.J. Pedersen, A. Jurys, M. Pedersen* Green Chem. 2020 22, 2399-2402
27. “Mechanistic study on the conversion of d-fructose into deoxyfructosazine: Insights from NMR and DFT study” L. Jia, Y. Qiao, M. Pedersen, S. Jia, H. Ma, Z. Zhang, Y. Wang, X. Hou Chem. Eng. Sci. 2020, 214, 115444
28. “Development and characterisation of mouse monoclonal antibodies specific for Clostridiodes (Clostridium) difficile lipoteichoic acid” C. Cairns, H. van Faassen, F. St. Michael, A. Aubry, K. Henry , M. Rossotti, S. Logan, G. Hussack, N. Gisch, W. Hogendorf, Pedersen, A. Cox ACS Chemical Biology 2020,15, 1050–1058
29. “Vessel Effect in C–F Bond Activation Prompts Revised Mechanism and Reveals an Autocatalytic Glycosylation” M.M. Nielsen Qiao  Y. Wang  C.M. Pedersen* Eur. J. Org. Chem. 2020, 140-144
30. “a-Selective Glycosylations using Glycosyl N-(ortho-Methoxyphenyl)trifluoroacetimidates” K. Kowalska, M. Pedersen* Org. Biol. Chem. 2020, 18, 1918-1925
31. “Palladium(0)-Catalyzed Rearrangement of Allylic Esters” B.M. Jessen, J.M. Ondozabal, M. Pedersen, A. Sølvhøj, E. Taarning, R. Madsen Chem. Select 2020, 5, 2559-2563
32. “Conformationally Switchable Glycosyl Donors” T. Holmstrøm, M. Pedersen* J. Org. Chem. 2019, 84, 13242-13251
33. “Self-promoted and stereospecific formation of N-glycosides” M. M. Nielsen, P. Mala, E. Baldursson, M. Pedersen* Chem. Sci. 2019, 10, 5299-5307
34. “NMR analysis of the Fischer-Tropsch process water: combination of 1D selective gradient TOCSY, 2D DOSY and qNMR” H. Ma, M. Pedersen, Q. Zhao, Z. Lyu, H. Chang, Y. Qiao, X. Hou, Y. Wang Anal. Chim. Acta 2019, 1066, 21-27
35. “Interaction between environmental contaminant PFOA and PAMAM in water: 19F and 1H NMR studies” C. Ning, H. Ma, M. Pedersen, H. Chang, Y. Wang, Y. Qiao Mol. Liq. 2019, 283, 45-50
36. “Synthesis of a-d-GalpN₃-(1-3)-d-GalpN₃: a- and 3-O-Selectivity Using 3,4-Diol Acceptors” E. Glibstrup, M. Pedersen* Beilstein J. Org. Chem. 2018, 14, 2805-2811
37. “Conformational distortion using a molecular lever: Galactoside derivatives” M. Häner, C. H. Hammelev, M. Pedersen* Eur. J. Org. Chem. 2018, 40, 5532-5537
38. “NMR studies of the tautomer distributions of D-fructose in lower alcohols/DMSO-d6” K. Shi, M. Pedersen, Z. Guo, Y. Li, H. Zheng,Y. Qiao, Y. Wang J. Mol. Liq. 2018 (DOI: 10.1016/j.molliq.2018.09.067)
39. “Catalytic Glycosylation in Oligosaccharide Synthesis” M.M. Nielsen andM. Pedersen* Chem. Rev. 2018, 118, 8285-8358
40. “DESs: green solvents and catalysts for the preparation of pyrazine derivatives by self-condensation of D-glucosamine” Wu, M.; Ma, H.; Ma, Z.; Jin, Y.; Chen, C.; Guo, X.; Qiao, Y.; Pedersen, C.; Hou, X.; Wang, Y. ACS Sus. Chem. Eng. 2018, 6, 9434-9441
41. “Ca²⁺-Assisted DOSYNMR: An Unexpected Tool for Anomeric Identification for d‑Glucopyranose” C. Ning, W. Ge, Z. Lyu, D. Luo, K. Shi, M. Pedersen, M.M. Nielsen, Y. Qiao, Y. Wang ChemistrySelect 2018, 3, 3943-3947
42. “Isomeric distribution of monosaccharides in deep eutectic solvents: NMR study” M. Wu, W. Zhou, M. Pedersen, H. Ma, Y. Qiao, X. Guo, X. Hou, Y. Wang J. Mol. Liq. 2018, 255, 244-249
43. “Combination of DOSY and 1D selective gradient TOCSY: versatile NMR tools for identify the mixtures from glycerol hydrogenolysis reaction” C. Li, J. Shan, X. Yan, D. Xiang, F, Yue, Y.-X. Wang, Z. Lyu, M. Pedersen, Y. Qiao FPT 2018, 171, 117-123
44. “NMR Studies of Stock Process Water and Reaction Pathways in Hydrothermal Carbonization of Furfural Residue” Y. Feng, M. Pedersen, X. Yan, Y. Liu, D. Xiang, C. Ning, Y. Wang, Y. Qiao Green Energy & Environment, 2018, 3, 163-171
45. “Graphene oxide: a novel acid catalyst for the synthesis of 2,5-dimethyl-N-phenyl pyrrole by the Paal-Knorr condensation” C.-Y. Chen, X.-Y. Guo, G.-Q. Lu, M. Pedersen, Y. Qiao, W.-L. Hou Y.-X. Wang New Carbon Mat. 2017, 32, 160-167
46. “Valorization of Furfural Residue by Hydrothermal Carbonization: Processing Optimization, Chemical and Structural Characterization” F. Yue, J. Zhang, M. Pedersen, Y. Wang, T. Zhao, P. Wang, Y. Liu, G. Qian, Y. Qiao ChemistrySelect 2017, 2, 583-590
47. “Product Distribution Control for Glucosamine Condensation: NMR Investigation Substantiated by Density-Functional Calculations” L. Jia, Z. Zhang, Y. Qiao, M. Pedersen, H. Ge, Z. Wei, T. Deng, J. Ren, X. Liu, Y.-X. Wang, X. Hou, Ind. Eng. Chem. Res. 2017, 56, 2925-2934
48. “On the nature of electronic effect of multiple hydroxyl groups in the 6-membered ring – the effects are additive but steric hindrance play a role too” M. Pedersen*, M. Bols, Org. Biomol. Chem. 2017, 15, 1154-1173
49. “Glycosyl Fluorides as Intermediates in the BF₃∙OEt₂ Promoted Glycosylation with Trichloroacetimidates” M.M. Nielsen, B.A. Stougaard, M. Bols, E. Glibstrup, M. Pedersen* Eur. JOC 2017, 1281-1284
50. “Catalytic stereospecific O-glycosylation” K. Kowalska, M. Pedersen* Chem. Commun. 2017, 53, 2040-2043
51. “Silyl protective groups influencing reactivity and selectivity in glycosylations” M. Bols, M. Pedersen* Beilstein JOC 2017, 13, 93-105
52. “Rhamnosylation: The solvent is the Solution” H. Elferink, M. Pedersen* Eur. J. Org. Chem.2017, 53-59
53. “Mechanism of the Self-condensation of GlcNH₂: Insights from in Situ NMR Spectroscopy and DFT Study” L. Jia, X. Liu, Y. Qiao, M. Pedersen, Z. Zhang, H. Ge, Z. Wei, Y. Chen, X. Wen, X. Hou, Y.X. Wang Applied Catalysis B: Environmental 2017, 202, 420-429
54. “Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot” M. Bandara, P. Yasomanee,   N.P. Rath,   C.M. Pedersen,*   M. Bols,* A.V. Demchenko* Org. Biomol. Chem. 2017, 15, 559-563
55. "NMR insights into the unexpected interaction of SnCl₄ with D-glucosamine and its effect on 5-HMF preparation in ZnCl₂ molten salt hydrate medium" C. Chen, W. Ge, L. Jia, M. Pedersen, Y. Qiao, S. Jia, X. Guo, Y. Wang, X. Hou ChemistrySelect 2016, 1, 6540-6545
56. “Scalable Synthesis of Anomerically Pure Orthogonal Protected GlcN₃ and GalN₃ from D-Glucosamine” E. Glibstrup, M. Pedersen* Org. Lett. 2016, 18, 4424-4427
57. “Glycosylation Intermediates Studied by Low Temperature ¹H- and ¹⁹F-DOSY NMR: New Insight into the Activation of Trichloroacetimidates.” Y. Qiao, W. Ge, L. Jia, Hou, Y. Wang, C.M. Pedersen* Chem. Commun. 2016, 52, 11418-11421
58. “Mechanism study of Cr(III) immobilization in the process of Cr(VI) removal by Huolinhe lignite” T.-T. Zhao, W.-Z. Ge, F. Yue, Y.-X.Wang, M. Pedersen, F.-G. Zeng, Y. Qiao Fuel Processing Technology 2016, 152, 375-380
59. "NMR study of the hydrolysis and dehydration of inulin in water: Comparison of the catalytic effect of Lewis acid SnCl4 and Brønsted acid HCl" Y. Qiao, M. Pedersen, D. Huang, W. Ge, M. Wu, C. Chen, S. Jia, Y.-X. Wang, W. Hou ACS Sustainable Chemistry & Engineering 2016, 4, 3327-3333
60. “C-H Functionalization of Carbohydrates” T.G. Frihed, M. Bols, M. Pedersen^* Eur. J. Org. Chem. 2016, 16, 2740-2756
61. “DOSY NMR: A Versatile Analytical Chromatographic Tool for Lignocellulosic Biomass Conversion” W. Ge, J.H. Zhang, M. Pedersen, T. Zhao, F. Yue, C. Chen, P. Wang, Y. Wang, Y. Qiao ACS Sustainable Chem. Eng., 2016, 4, 1193-1200
62. “Super Arming of a Glycosyl Donor Using a Molecular Lever” J. I. Olsen, K. Kowalska, M. Pedersen^* and M. Bols^* Tetrahedron Lett. 2016, 57, 35-38
63. “Pyrolysis of chitin biomass: TG-MS analysis and solid char residue characterization” Y. Qiao, S. Chen, Y. Liu, H. Sun, S. Jia, J. Shi, M. Pedersen, Y. Wang, X. Hou Carbohydr. Polymers 2015, 130, 163-170
64. “Glucosamine condensation catalysed by 1-ethyl-3-methylimidazolium acetate: mechanistic insight from NMR spectroscopy” Jia, C.M. Pedersen, Y. Qiao, T. Deng, P. Zuo, W. Ge, Z. Qin, X. Hou, Y. Wang Physical Chemistry Chemical Physics 2015, 17, 23173-23182
65. “β-Mannosylation with 4,6-benzylidene protected mannosyl donors without preactivation” M. Heuckendorff, P. S. Bols, C. Barry, T. G. Frihed, M. Pedersen*, M. Bols^* Chem. Commun. 2015, 51, 13283-13285
66. “A fluorescence study of isofagomine protonation in β-glucosidase” E. Lindback, B.W. Laursen, J.C.N. Poulsen, K. Kilså, M. Pedersen, M. Bols Org. Biomol. Chem. 2015, 13, 6562-6566
67. “Synthesis of l-Hexoses” T. Frihed, Bols, M. Pedersen* Chem. Rev. 2015, 115, 3615-3676
68. “Mechanisms of Glycosylation Reactions Studied by Low Temperature NMR” T. Frihed, M. Bols, M. Pedersen* Chem. Rev. 2015, 115, 4963-5013
69. ”Exploring the relationship between conformation and pKa: Can a pKa value be used to determine the conformational equilibrium?” J. I. Olsen, M. Pedersen^*, M. Bols Org. Biomol. Chem. 2015, 13, 3116-3121
70. “In situ NMR spectroscopy: Inulin biomass conversion in ZnCl₂ molten salt hydrate medium—SnCl₄ addition controls product distribution” Y. Wang, M. Pedersen, Y. Qiao, T. Deng, J. Shi, X. Hou Carbohydr. Polymers 2015, 115, 439-443
71. “NMR Insights on the properties of ZnCl2 Molten Salt Hydrate Medium through its Interaction with SnCl₄ and Fructose” Y. Qiao, M. Pedersen, Y. Wang, X. Hou ACS Sus. Chem. & Eng. 2014, 2, 2576-2581
72. ”Synthesis of All Eight Stereoisomeric 6-Deoxy-L-Hexopyranosyl Donors – Trends in Using Stereoselective Reductions or Mitsunobu Epimerizations” T. G. Frihed, C.M. Pedersen*, Bols* Eur. JOC 2014, 35, 7924
73. ”Synthesis of All Eight L-Glycopyranosyl Donors Using C-H Activation” T.G. Frihed, M. Pedersen*, M. Bols* Angew. Chem. Int. Ed. 2014, 53, 13889
74. “Human L-ficolin recognizes phosphocholine moieties of pneumococcal teichoic acid” E. Stermann, M. Lacroix, E. Gout, E. Lafly, M. Pedersen, L. Martin, A. Amoroso, R.R. Schmidt, U. Zähringer, C. Gaboriaud, A.M. Di Guilmi, N.M. Thielens J. Immunol. 2014, 193, 5699-5708
75. “Total Synthesis of Five Lipoteichoic acids of Clostridium difficile” W.F.J. Hogendorf, N. Gisch, D. Schwudke, H. Heine, M. Bols, M. Pedersen* Chem. Eur. J. 2014, 20, 13511 – 13516
76. “Cyclodextrin-based artificial oxidases with high rate accelerations and selectivity” Y. Zhou, E.A. Lindbäck, M. Pedersen, M. Bols Tetrahedron Lett. 2014, 55, 2304-2307
77. “β-Selective mannosylation with a 4, 6-silylene-tethered thiomannosyl donor” M. Heuckendorff, M. Pedersen*, M. Bols* Org. Lett. 2014, 16, 1116-1119
78. “Synthesis and thermotropic phase behavior of four glycoglycerolipids” W.F.J. Hogendorf, V. Jagalski, T.G. Pomorski, M. Bols, M. Cárdenas, M. Pedersen* Molecules 2013, 18, 13546-13573
79. “Superarming of Glycosyl Donors by Combined Neighboring and Conformational Effects” M. Heuckendorff, H.D. Premathilake, P. Pornsuriyasak, A.Ø. Madsen, M. Pedersen,* M. Bols, A.V. Demchenko Org. Lett. 2013, 15, 4904-4907
80. “Conformationally armed 3, 6-tethered glycosyl donors: synthesis, conformation, reactivity, and selectivity” M. Heuckendorff, M. Pedersen,* M. Bols* J. Org. Chem. 2013, 78, 7234-7248
81. “Direct conversion of chitin biomass to 5-hydroxymethylfurfural in concentrated ZnCl2 aqueous solution” Y. Wang, M. Pedersen, T. Deng, Y. Qiao, X. Hou Bioresour. Technol. 2013, 143, 384-390
82. “Diethyl silane” T. G. Frihed, M. Bols, M. Pedersen* e-EROS Encyclopedia of Reagents for Organic Synthesis (Online, 2013)
83. “Enzyme inhibition by iminosugars: Analysis and insight into the glycosidase–iminosugar dependency of pH” Ó. López, F.L. Qing, M. Pedersen, M. Bols Bio. Org. Med. Chem. 2013 (Online)
84. “Artificial enzyme activity from cyclodextrins with cyanohydrins on the secondary rim” Y. Zhou, M. Pedersen, M. Bols Tetrahedron Lett. 2013, 54, 2458-2461
85. “Influence of O6 in mannosylations using benzylidene protected donors: stereoelectronic or conformational effects?” T.G. Frihed, M.T.C. Walvoort, J.D.C. Codée, G.A. van der Marel, M. Bols, M. Pedersen* J. Org. Chem. 2013, 78, 2191-2205
86. “Total synthesis of biologically active lipoteichoic acids” M. Pedersen*, M. Bols, Y. Qiao ARKIVOC 2013, 2, 249-275
87. ”Easy Access to L‐Mannosides and L‐Galactosides by Using C-H Activation of the Corresponding 6‐Deoxysugars” T.G. Frihed, M. Heuckendorff, M. Pedersen*, M. Bols* Angew. Chem. Int. Ed. 2012, 51, 12285-12288
88. “Synthesis of Tin‐Containing Cyclodextrins as Potential Enzyme Models” Y. Zhou, L. Marinescu, M. Pedersen, M. Bols Eur. J. Org. Chem. 2012, 32, 6383-6389
89. “Molecular and functional characterization of the interaction of L-ficolin with Streptococcus pneumoniae” E. Stermann, M. Lacroix, E. Gout, E. Laffly, M. Pedersen, R. R. Schmidt, T. Vernet, C. Gaboriaud, A.-M. Di Guilmi, N.M. Thielens Immunobiology 2012, 217, 1188-1189
90. “Synthesis of cyclodextrins with carboxylic acids at the secondary rim and an evaluation of their properties as chemzymes for glycoside hydrolysis” Y. Zhou, E. Lindbaeck, L.G. Marinecsu, M. Pedersen, M. Bols Eur. J. Org. Chem. 2012, 27, 4063-4070
91. “Artificial enzymes based on cyclodextrin with phenol as the catalytic group” E. Lindbäck, Y. Zhou, M. Pedersen*, M. Bols* Tetrahedron Letters 2012, 53, 5023-5026
92. ”Two diastereomeric artificial enzymes with different catalytic activity” E. Lindbäck, M. Pedersen, M. Bols Eur. J. Org. Chem. 2012, 27, 5366-5372
93. “Rhamnosylation: diastereoselectivity of conformationally armed donors” M. Heuckendorff, M. Pedersen*, M. Bols J. Org. Chem. 2012, 77, 5559-5568
94. “A uronic acid analogue of isofagomine lactam as a nanomolar glucuronidase inhibitor” E. Lindback, Y. Zhou, Ó. López, J. G. Fernández-Bolaños, M. Pedersen, M. Bols Tetrahedron Letters 2012, 53, 2045-2047
95. ”Conversion of d-glucose into 5-hydroxymethylfurfural (HMF) using zeolite in [Bmim]Cl or tetrabutylammonium chloride (TBAC)/CrCl₂” H. Jadhav, E. Taarning, M. Pedersen, M. Bols Tetrahedron Letters 2012, 53, 983-985
96. ”Synthesis of the repeating unit of the lipoteichoic acid of Streptococcus pneumoniae” M. Pedersen*, I. Figueroa-Perez, A.J. Ulmer, U. Zähringer R.R. Schmidt Tetrahedron 2012, 68, 1052-1061
97. “The influence of neighboring group participation on the hydrolysis of 2-O-substituted methyl glucopyranosides” M. Heuckendorff, M. Pedersen*, M. Bols Organic Letters 2011, 13, 5956-5959
98. “3‐Deoxy‐glucosone is an Intermediate in the Formation of Furfurals from D‐” H. Jadhav, C.M. Pedersen, T. Sølling, M. Bols ChemSusChem 2011, 4, 1049-1051
99. “A study of anhydrocelluloses–Is a cellulose structure with residues in a 1 C 4-conformation more prone to hydrolysis?” V. Jadhav, M. Pedersen*, M. Bols Org. Biol. Chem. 2011, 9, 7525-7534
100. “Recognition of Peptides by Cyclodextrin Trimers” H.S. Christensen, B.W. Sigurskjold, T.G. Frihed, L. Marinescu, M. Pedersen, M. Bols Eur. J. Org. Chem. 2011, 27, 5279-5290
101. “Quantifying the Electronic Effects of Carbohydrate Hydroxy Groups by Using Aminosugar Models” M. Pedersen*, J. I. Olsen, A. Brka, M. Bols* Chem. Eur. J. 2011, 17, 7080-7086
102. ”Chemical synthesis of bacterial lipoteichoic acids: an insight on its biological significance” U. Zähringer, M. Pedersen, Y. Qiao, R.R. Schmidt Org. Biol. Chem. 2011, 9, 2040-2052
103. “Glycosyl donors in “unusual” conformations–influence on reactivity and selectivity” M.Pedersen, L. G. Marinescu, M. Bols Compt. Rend. Chim. 2011, 14, 17-43
104. “Synthesis of 5‐Bromomethylfurfural from Cellulose as a Potential Intermediate for Biofuel” N. Kumar, J. Olsen, M. Pedersen, M. Bols Eur. J. Org Chem.2011, 7, 1266-1270
105. “Quantifying electronic effects of common carbohydrate protecting groups in a piperidine model system” M. Heuckendorff, M. Pedersen*, M. Bols Chem. Eur. J. 2010, 16, 13982-94 (VIP paper)
106. “The Grignard Reaction of Cyclodextrin‐6‐aldehydes Revisited: A Study of the Stereoselectivity Upon Addition of Organometallic Reagents to Aldehydes and Ketones” E. Lindback, Y. Zhou, L.G. Marinescu, M. Pedersen, M. Bols Eur. J. Org. Chem. 2010, 20, 3883-96
107. “Synthesis of the core structure of the lipoteichoic acid of Streptococcus pneumoniae” M. Pedersen, I. Figueroa-Perez, J. Boruwa, B. Lindner, A.J. Ulmer, U. Zähringer R.R. Schmidt Chem. Eur. J. 2010, 16, 12627-41
108. “Total synthesis of lipoteichoic acid of Streptococcus pneumoniae” M. Pedersen, I. Figueroa-Perez, B. Lindner, A.J. Ulmer, U. Zähringer R.R. Schmidt Angew. Chem.Int. Ed. 2010 49, 2585-90 (“Hot Paper”)
109. “An extended study of dimeric phenyl tropanes” S. Nielsen, M. Pedersen, S.G. Hansen, M.D. Petersen, S. Sinning, O. Wiborg, H.H. Jensen, M. Bols Bioorganic & Medicinal Chemistry, 2009, 17, 4900-9
110. “Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions” M. Pedersen, L.G. Marinescu, M. Bols Chem. Commun. 2008, 2465-2467
111. “Going to extremes:“super” armed glycosyl donors in glycosylation chemistry” H.H. Jensen, M. Pedersen, M. Bols, Chem. Eur. J., 2007,  13,  7576-7582
112. ““Super armed” glycosyl donors: conformational arming of thioglycosides by silylation” M. Pedersen, L.-U. Nordstrøm, M. Bols, J. Am. Chem. Soc. 2007,129, 9222-9235
113. “On the use of 3, 5-O-benzylidene and 3, 5-O-(di-tert-butylsilylene)-2-O-benzylarabinothiofuranosides and their sulfoxides as glycosyl donors for the synthesis of β-arabinofuranosides: importance of the activation method” D. Crich, M. Pedersen, A.A. Bowers, Wink, D. J. Org. Chem. 2007, 72, 1553-1565
114. “Stereochemical substituent effects: investigation of the cyano, amide and carboxylate group” M. Pedersen, M. Bols Tetrahedron, 2005, 61, 115-122
115. ”On the electronic effects of OH groups. Synthesis and investigation of tetrahydroxylated azabicycloheptanes” A. Gregersen, M. Pedersen, H. H. Jensen, M. Bols Org. Biomol. Chem. 2005, 3, 1514-1519
116. “Radical substitution with azide: TMSN₃–PhI(OAc)₂ as a substitute of IN₃” M. Pedersen, L.G. Marinescu, M. Bols Org. Biomol. Chem., 2005, 3, 816.
117. “Safe radical azidonation using polystyrene supported diazidoiodate (I)” L.G. Marinescu, M. Pedersen, M. Bols Tetrahedron, 2005, 61, 123-127.