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  1. Highly homogeneous and robust PolyProline type I helices from peptoids with non-aromatic α-chiral side chains
    Roy O., Dumonteil G., Faure S., Jouffret L., Kriznik A., Taillefumier C. J. Am. Chem. Soc. 2017, 139, 13533–13540.

  2. 1,2,3-Triazolium-based peptoid oligomers
    Aliouat H., Caumes C., Roy O., Zouikri M., Taillefumier C., Faure S. J. Org. Chem. 2017, 82, 2386–2398.

  3. Antioxidant Activities of Peptoid-Grafted Chitosan Films
    Elchinger P-H., Delattre C., Faure S., Roy O., Badel S., Bernardi T., Michaud P., Taillefumier C. Appl. Biochem. Biotechnol. 2017, 181, 283-293.

  4. Selective complexation of divalent cations by a cyclic α,β-peptoid hexamer: a spectroscopic and computational study
    De Santis E., Edwards A. A., Alexander B. D., Holder S. J., Biesse-Martin A.-S., Nielsen B. V., Mistry D., Waters L., Siligardi G., Hussain R., Faure S., Taillefumier C. Org. Biomol. Chem 2016, 17, 11371-11380.

  5. Weak backbone CH⋯O=C and side chain tBu⋯tBu London interactions help promote helix folding of achiral NtBu peptoids _ Angelici G., Bhattacharjee N., Roy O., Faure S., Didierjean C., Jouffret L., Jolibois F., Perrin L., Taillefumier C. Chem. Commun. 2016, 52, 4573-4576.

  6. Multivalent thioglycopeptoids via photoclick chemistry: potent affinities towards LecA and BC2L-A lectins
    Caumes C., Gillon E., Legeret B., Taillefumier C., Imberty A., Faure S. Chem. Commun. 2015, 51, 12301-12304.

  7. Immobilization of proteases on chitosan for the development of films with antibiofilm properties.
    Elchinger P.-H., Delattre C., Faure S., Roy O., Badel S., Bernardi T., Taillefumier C., Michaud P. International Journal of Biological Macromolecules 2015, 72, 1063-1068.

  8. Effect of proteases against biofilms of Staphylococcus aureus and Staphylococcus epidermidis.
    Elchinger P.-H., Delattre C., Faure S., Roy O., Badel S., Bernardi T., Taillefumier C., Michaud P. Letters in Applied Microbiology 2014, 59, 507-513.

  9. Rapid and convenient semi-automated microwave assisted solid-phase synthesis of arylopeptoids.
    Rasmussen J. E., Boccia M. M., Nielsen J., Taillefumier C., Faure S. Hjelmgaard T. Tetrahedron Lett. 2014, 55, 5940–5943.

  10. From Glycopeptides to Glycopeptoids.
    Szekely T., Roy O., Faure S., Taillefumier C. Eur. J. Org. Chem. 2014, 5641–5657.

  11. Macrocyclic Arylopeptoids – A Novel Type Of Cyclic N-Alkylated Aromatic Oligoamides Forming Nanotubular Assemblies
    Hjelmgaard T., Roy O., Nauton L., El-Ghozzi M., Avignant D., Didierjean C., Taillefumier C., Faure S. Chem. Commun. 2014, 50, 3564-3567.

  12. Cyclic α,β-Tetrapeptoids: Sequence-Dependent Cyclization And Conformational Preference
    Caumes C., Fernandes C., Roy O., Hjelmgaard T., Wenger E., Didierjean C., Taillefumier C., Faure S. Org. Lett. 2013, 15, 3626-3629.

  13. The Tert-Butyl Side Chain: A Powerful Means To Lock Peptoid Amide Bonds In The Cis Conformation.
    Roy O., Caumes C., Esvan y., Didierjean C., Faure S., Taillefumier C. Org. Lett. 2013, 15, 2246-2249.

  14. Molecular Structures Of The Photodimers Of 5-Phenyluracil And 6-Phenyluracil.
    Vidal A., Paugam R., Guillot R., Faure S., Pereira E., Aitken D. J. Tetrahedron Lett. 2013, 54, 2536-2537.

  15. α-Peptoïdes Et Composés Apparentés : Synthèse Et Contrôle De La Conformation (α-Peptoids And Related Compounds: Synthesis And Control Of The Conformation).
    Szekely T., Caumes C., Roy O., Faure S., Taillefumier C. C. R. Chimie 2012, 16, 318-330.

  16. Synthesis And Binding Affinities For Sst Receptors Of Cyclic Peptoid SRIF-Mimetics
    Caumes C., Hjelmgaard T., Roy O., Reynaud M., Servent D., Taillefumier C., Faure S.Med. Chem. Commun. 2012, 3, 1531-1535.

  17. Pharmacological And Structural Characterization Of Conformationally Restricted (S)-Glutamate Analogues At Ionotropic Glutamate Receptors
    Juknaitė L., Venskutonytė R., Assaf Z., Faure S., Gefflaut T., Aitken D. J., Nielsen B., Gajhede M., Kastrup J.S., Bunch L., Frydenvang K., Pickering D.S. J. Of Structural Biology 2012, 180, 39-46.

  18. Improved solid-phase synthesis and study of arylopeptoids with conformation-directing side chains.
    Hjelmgaard T., Faure S., De Santis E., Staerk D., Alexander B.D., Edwards A. A., Taillefumier C., Nielsen J. Tetrahedron 2012, 68, 4444-4454. (invitation, special issue of Tetrahedron (Symposium in print) on Chemistry of Foldamers).

  19. The Click Triazolium Peptoid Side Chain: A Strong cis-Amide Inducer Enabling Chemical Diversity.
    Caumes C., Roy O., Faure S., Taillefumier C. J. Am. Chem. Soc. 2012, 134, 9553-9556.

  20. Synthesis of new C-glycosyl aza- β3-amino acids building blocks.
    Andreini M., Felten A.S., Thien H.T.T., Taillefumier C., Pellegrini-Moïse N., Chapleur Y. Tetrahedron Lett. 2012, 53, 2702-2705.

  21. Effect of capping groups at the N- and C-termini on the conformational preference of α,β-peptoids.
    De Santis E., Hjelmgaard T., Caumes C., Faure S., Alexander B.D., Holder S.J., Siligardi G., Taillefumier C., Edwards A.A. Org. Biomol. Chem. 2012, 10, 1108-1122.

  22. Highly Convenient Gram-Scale Solution-Phase Peptoid Synthesis and Orthogonal Side-Chain Post-Modification.
    Caumes C., Hjelmgaard T., Remuson R., Faure S., Taillefumier C. Synthesis 2011, 257-264.

  23. Selectivity among Two Lectins: Probing the Effect of Topology, Multivalency and Flexibility of "Clicked" Multivalent Glycoclusters.
    Cecioni S., Faure S., Darbost U., Bonnamour I., Parrot-Lopez H., Roy O., Taillefumier C., Wimmerova M., Praly J.P., Imberty A., Vidal S. Chem. Eur. J. 2011, 17, 2146-2159.

  24. Cyclic α,β-peptoid octamers with differing side chain patterns: synthesis and conformational investigation.
    De Santis E., Hjelmgaard T., Faure S., Roy O., Didierjean C,. Alexander B.D., Siligardi G., Hussain R., Javorfi T., Edwards A.A., Taillefumier C. Amino Acids 2011, 41, 663-672.

  25. Efficient and versatile COMU-mediated solid-phase submonomer synthesis of arylopeptoids (oligomeric N-substituted aminomethyl benzamides).
    Hjelmgaard T., Faure S., Staerk D., Taillefumier C., Nielsen J. Org. Biomol. Chem. 2011, 9, 6832-6843.

  26. Expedient Solution-Phase Synthesis and NMR Studies of Arylopeptoids.
    Hjelmgaard T., Faure S., Staerk D., Taillefumier C., Nielsen J. Eur. J. Org. Chem. 2011, 4121-4132.

  27. Click glycoconjugation of per-azido- and alkynyl-functionalized β-peptides built from aspartic acid.
    Barra M., Roy O., Traikia M., Taillefumier C. Org. Biomol. Chem. 2010, 8, 2941-2955.

  28. 12-Helix Folding of Cyclobutane β-Amino Acid Oligomers.
    Fernandes C., Faure S., Pereira E., Thery V., Declerck V., Guillot R., Aitken D.J. Org. Lett. 2010, 12, 3606-3609.

  29. Convenient Solution-Phase Synthesis and Conformational Studies of Novel Linear and Cyclic α,β-Alternating Peptoids.
    Hjelmgaard T., Faure S., Caumes C., De Santis E., Edwards A.A., Taillefumier C. Org. Lett. 2009, 11, 4100-4103.

  30. Expedient preparation of all isomers of 2-Aminocyclobutanecarboxylic acid in enantiomerically pure form.
    Fernandes C., Pereira E., Faure S., Aitken D.J. J. Org. Chem. 2009, 74, 3217-3220.

  31. Synthesis and Solution Conformation of Homo-β-peptides Consisting of N-Mannofuranosyl-3-ulosonic acids.
    Andreini M., Taillefumier C., Chretien F., Thery V., Chapleur Y. J. Org. Chem. 2009, 74, 7651-7659.

  32. An Efficient Route to Acyclic C-Nucleosides and Fused-Ring Analogues of Uridine from exo-Glycals.
    Enderlin G., Taillefumier C., Didierjean C., Chapleur Y. J. Org. Chem. 2009, 74, 8388-8391.

  33. Passerini Reaction-Amine Deprotection-Acyl Migration (PADAM) Peptide Assembly: Efficient Formal Synthesis of Cyclotheonamide C.
    Faure S., Hjelmgaard T., Roche S. P., Aitken D. J. Org. Lett. 2009, 11, 1167-1170.

  34. Total Synthesis of Cyclotheonamide C by Use of an α-Keto Cyanophosphorane Methodology for Peptide Assembly.
    Roche S. P., Faure S., El Blidi L., Aitken D. J. Eur. J. Org. Chem. 2008, 5067-5078.

  35. Total Synthesis of Cyclotheonamide C using a Tandem Backbone-Extension-Coupling Methodology.
    Roche S. P., Faure S., Aitken D. J. Angew. Chem. Int. Ed. 2008, 47, 6840-6842.

  36. Synthesis of sugar β-amino acid containing homooligomeric cyclic peptides.
    Andreini M., Taillefumier C., Fernette B., Chapleur Y. Lett. Org. Chem. 2008, 5, 360-364.

  37. Cyclic β-peptoids.
    Roy O., Faure S., Thery V., Didierjean C., Taillefumier C. Org. Lett. 2008, 10, 921-924.

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