62. Kondratieva A, Palica K, Frøhlich C, Hovd RR, Leiros HKS, Erdelyi M, Bayer A. Eu. J. Med. Chem., 2024, accepted. Fluorinated Captopril Analogues Inhibit Metallo-ß-Lactamases and Facilitate Structure Determination of NDM-1 Binding Pose. Open access! doi: 10.1016/j.ejmech.2024.116140

61. Langer MK, Rahman A, Dey H, Andersen T, Haug T, Blencke HM, Stensvåg K, Strøm MB, Bayer A. Eu. J. Med. Chem., 2023, 115147. Investigation of Tetrasubstituted Heterocycles Reveals Hydantoins as a Promising Scaffold for Development of Novel Antimicrobials with Membranolytic Properties. Open access! doi: 10.1016/j.ejmech.2023.115147

60. Sousa A, Borøy V, Bæverud A, Julin K, Bayer A, Strøm M, Johannessen M, Škalko-Basnet N, Obuobi S.  J. Mater. Chem. B, 2023, 7972. Polymyxin B stabilized DNA micelles for sustained antibacterial and antibiofilm activity against P. aeruginosa. Open access! doi: 10.1039/D3TB00704A 

59. Hemmingsen LM, Giordani B, Paulsen MH, Vanic Z, Flaten GE, Vitali B, Basnet P, Bayer A, Strøm MB, Skalko-Basnet N. Biomat. Adv. 2023, 213238.  Tailored anti-biofilm activity – liposomal delivery for mimic of small antimicrobial peptide. Open access! doi: 10.1016/j.bioadv.2022.213238

58. von Hofsten S, Langer M, Korelin K, Magnussen S, Ausbacher D, Andersen T, Salo T, Strøm MB, Bayer A, Berge G. Front. Pharmacol. 2023, Amphipathic barbiturates as marine product mimics with cytolytic and immunogenic effects on head and neck squamous cell carcinoma cell lines. Open access! doi: 10.3389/fphar.2023.1141669

57. von Hofsten S, Paulsen MH, Magnussen SN, Ausbacher D, Kranz M, Bayer A, Strøm MB, Berge G. Sci. Rep., 2022, 15586. The marine natural product mimic MPM-1 is cytolytic and induces DAMP release from human cancer cell lines. Open access! doi: 10.1038/s41598-022-19597-4

56. Langer MK, Rahman A, Dey H, Andersen T, Zilioli F, Haug T, Blencke HM, Stensvåg K, Strøm MB, Bayer A. Eu. J. Med. Chem., 2022, 114632. A concise SAR-analysis of antimicrobial cationic amphipathic barbiturates for an improved activity-toxicity profile. Open access! doi: 10.1016/j.ejmech.2022.114632

55. Wieske LHE, Bogaerts J, Leding AAM, Wilcox S, Rasmussen AA, Leszczak K, Turunen L, Herrebout WA, Hubert M, Bayer A, Erdélyi M. ACS Med. Chem. Lett., 2022, 257-61. NMR Backbone Assignment of VIM-2 and Identification of the Active Enantiomer of a Potential Inhibitor. Open access! doi: 10.1021/acsmedchemlett.1c00635

54. Gevorgyan A, Hopmann HK, Bayer A. Organometallics, 2022, 1777-85. Improved Buchwald–Hartwig Amination by the Use of Lipids and Lipid ImpuritiesOpen access! doi: 10.1021/acs.organomet.1c00517.

53. Gevorgyan A, Hopmann HK, Bayer A. Green Chemistry, 2021, 7219-27. Lipids as Versatile Solvents for Chemical Synthesis. UiT´s open research archive; doi: 10.1039/D1GC02311J.

52. Paulsen MH, Engqvist M, Ausbacher D, Andersen T, Langer MK, Haug T, Morello GR, Liikanen LE, Blencke HM, Isaksson J, Juskewitz E, Bayer A, Strøm MB. J. Med. Chem., 2021,11395. Amphipathic Barbiturates as Mimics of Antimicrobial Peptides and the Marine Natural Products Eusynstyelamides with Activity Against Multi-Resistant Clinical Isolates. Open access! doi: 10.1021/acs.jmedchem.1c00734.

51. Pavlovic L, Pettersen M, Gevorgyan A, Vaitla J, Bayer A, Hopmann HK. Eur. J. Org. Chem., 2021, 663. Computational and experimental insights into asymmetric Rh-catalyzed hydrocarboxylation with CO2. Open access! doi: 10.1002/ejoc.202001469.

50. Guttormsen Y, Fairhorst M, Pandey SK, Isaksson J, Haug BE, Bayer A. Molecules, 2020, 4848. Total synthesis of Phorbazole B. Open access! doi: 10.3390/molecules25204848.

49. Ikenna E. Ndukwe IE, Lam Y-H, Pandey SK, Haug BE, Bayer A, Sherer EC, Blinov KA, Williamson RT, Isaksson J, Reibarkh M, Liu Y, Martin GE. Chem. Sci., 2020, 12081. Unequivocal Structure Confirmation of a Breitfussin Analog by Anisotropic NMR Measurements. Open access! doi: 10.1039/D0SC03664A.

48. Ismael A, Gevorgyan A, Skrydstrup T, Bayer, A. Org. Process Res. Dev., 2020, 2665. Renewable Solvents for Palladium-Catalyzed Carbonylation ReactionsOpen access! doi: 10.1021/acs.oprd.0c00325.

47. Muhammad Z, Skagseth S, Akhter S, Fröhlich C, Christopheit T, Bayer A, Leiros HKS. Bioorg. Med. Chem., 2020, 115598. Structural studies of triazole inhibitors with promising inhibitor effects against antibiotic resistance metallo-β-lactamases. Open access! doi: 10.1016/j.bmc.2020.115598.

46. Samuelsen Ø, Åstrand OAH, Fröhlich C, Heikal A, Skagseth S, Carlsen TJO, Leiros HKS, Bayer A, Schnaars C, Kildahl-Andersen G, Lauksund S, Finke S, Huber S, Gjøen T, Andresen AMS, Økstad OA, Rongved P. Antimicrob. Chemother. Agents , 2020, e02415. ZN148–a modular synthetic metallo-β-lactamase inhibitor reverses carbapenem-resistance in Gram-negative pathogens in vivo. Open access! doi: 10.1128/AAC.02415-19.

45. Ismael A, Skrydstrup T, Bayer A. Org. Bioorg. Chem., 2020, 1754. Carbonylative Suzuki-Miyaura couplings of sterically hindered aryl halides: Synthesis of 2-aroylbenzoate derivatives. UiT´s open research archive; doi: 10.1039/D0OB00044B.

44. Gevorgyan A, Hopmann HK, Bayer A. Chem. Eur. J. 2020, 6064. Formal C-H carboxylation of unactivated arenes with carbon dioxide. Open access! doi: 10.1002/chem.202000515. Featured in Org. Chem. Highlights 12th oct. 2020: Substituted Benzenes!

43. Gevorgyan A, Hopmann HK, Bayer A. ChemSusChem, 2020, 2080. Exploration of New Biomass-Derived Solvents: Application to Carboxylation Reactions. Open access! doi:10.1002/cssc.201903224.

42. Obst M, Gevorgyan A, Bayer A, Hopmann HK. Organometallics, 2020, 1545. Mechanistic insights into copper-catalysed carboxylations. UiT´s open research archive; doi:10.1021/acs.organomet.9b00710.

41. Hansen K, Andersen J, Bayer A, Pandey S, Lorentzen M, Jørgensen K, Sydnes M, Guttormsen Y, Baumann M, Klebl B, Eickhoff J, Haug B, Isaksson J, Hansen E. J. Med. Chem. 2019, 10167Kinase Chemodiversity from the Arctic: The Breitfussins. UiT´s open research archive; doi: 10.1021/acs.jmedchem.9b01006.

40. Gevorgyan A, Obst M, Maseras F, Hopmann HK, Bayer A. Chem. Sci. 2019, 10072. Caesium-Fluoride Mediated Hydrocarboxylation of Alkenes and Allenes: Scope and Mechanistic Insight. Open access! doi: 10.1039/c9sc02467k.

39. Paulsen MH, Ausbacher D, Bayer A, Engqvist M, Hansen T, Haug T, Anderssen T, Anderssen JH, Sollid JUE, Strøm MB. Eur. J. Med. Chem. 2019, 111671. Antimicrobial activity of amphipathic α,α-disubstituted β-amino amide derivatives against ESBL – CARBA producing multi-resistant bacteria; effect of halogenation, lipophilicity and cationic character. Open access! doi: 10.1016/j.ejmech.2019.111671.

38. Vaitla J, Bayer A, Hopmann KH. Synlett. 2019, 1377. Vinyl Sulfoxonium Ylide: A New Vinyl Carbenoid Transfer Reagent for the Synthesis of Heterocycles. UiT´s open research archive; doi: 10.1055/s-0037-1611771.

37. Vaitla J, Bayer A. Synthesis 2019, 612. Sulfoxonium ylide derived metal carbenoids in organic synthesis. UiT´s open research archive; doi: 10.1055/s-0037-1610328.

36. Vaitla J, Bayer A, Hopmann KH. Ang. Chem. Int. Ed. 2018, 16180. Iron‐Catalyzed Carbenoid Transfer Reactions of Vinyl Sulfoxonium Ylides: An Experimental and Computational Study. UiT´s open research archive; doi: 10.1002/anie.201810451.

35. Paulsen MH, Karlsen EA, Ausbacher D, Andersen T, Bayer A, Ochtrop P, Hedberg C, Haug T, Sollid JUE, Strøm MB. J. Pep. Sci. 2018, 24:e3117. An amphipathic cyclic tetrapeptide scaffold containing halogenated β 2,2-amino acids with activity against multi-resistant bacteria. doi: 10.1002/psc.3117.

34. Pavlovic L, Vaitla J, Bayer A, Hopmann KH. Organometallics 2018, 941. Rhodium-Catalyzed Hydrocarboxylation: Mechanistic Analysis Reveals Unusual Transition State for Carbon-Carbon Bond Formation. UiT´s open research archive; doi: 10.1021/acs.organomet.7b00899.

33. Fairhurst M, Zeeshan M, Haug BE, Bayer A. Synlett 2018, 1303. Aldol condensations on a 3-alkylidene-2,5-diketopiperazine –  synthesis of two marine natural products. UiT´s open research archivedoi: 10.1055/s-0036-1591755

32. Akhter S, Lund BA, Ismael A, Lange M, Christopeit T, Leiros HKS, Bayer A. Eur. J. Med. Chem. 2018, 634. A focused fragment library targeting the antibiotic resistance enzyme – Oxacillinase-48: synthesis, structural evaluation and inhibitor design. UiT´s open research archive; doi: 10.1016/j.ejmech.2017.12.085

31. Hansen K, Isaksson J, Bayer A, Johansen J, Andersen JH, Hansen E. J. Nat. Prod. 2017, 3276. Securamine Derivatives from the Arctic Bryozoan Securiflustra securifrons. doi: 10.1021/acs.jnatprod.7b00703

30. Vaitla J, Hopmann KH, Bayer A. Org. Lett. 2017, 6688. Rhodium-Catalyzed Synthesis of Sulfur Ylides via in Situ Generated Iodonium Ylides. UiT´s open research archive; doi: 10.1021/acs.orglett.7b03413

29. Vaitla J, Guttormsen Y, Mannisto JK, Nova A, Repo T, Bayer A, Hopmann KH. ACS Catalysis 2017, 7231. Enantioselective Incorporation of CO2: Status and Potential. UiT´s open research archive; doi: 10.1021/acscatal.7b02306

28. Skagseth S, Christopeit T, Akhter S, Bayer A, Samuelsen Ø, Leiros HKS. Antimicrob. Chemother. Agents 61, 2017, e02602. Structural insights into TMB-1 and the role of residue 119 and 228 in substrate and inhibitor activity. UiT´s open research archive; doi: 10.1128/AAC.02602-16

27. Vaitla J, Bayer A, Hopmann KH. Ang. Chem. Int. Ed. 2017, 4277. Synthesis of Indoles and Pyrroles Utilizing Iridium Carbenes Generated from Sulfoxonium Ylides. UiT´s open research archive; doi:10.1002/anie.201610520. Featured in Org. Chem. Highlights 16th Oct 2017: Heterocycle construction!

26. Skagseth S, Akhter S, Paulsen MH, Muhammad Z, Samuelsen Ø, Leiros HKS, Bayer A. Eur. J. Med.Chem. 135, 2017, 159. Metallo-β-lactamase inhibitors by bioisosteric replacement: preparation, activity and binding. UiT´s open research archive; doi: 10.1016/j.ejmech.2017.04.035

25. Paulsen MH, Engqvist M, D. Ausbacher, Strøm MB, Bayer A. Org. Biomol. Chem. 2016, 7570. Efficient and scalable synthesis of α,α-disubstituted β–amino amides. Open access! doi10.1039/C6OB01219A

24. Lund BA, Guttormsen Y, Christopeit T, Bayer A, Leiros HKS. J. Med. Chem. 2016, 5542. Screening and Design of Inhibitor Scaffolds for the Antibiotic Resistance Oxacillinase-48 (OXA-48) through Surface Plasmon Resonance Screening. UiT´s open research archive; doi: 10.1021/acs.jmedchem.6b00660.

23. Lorentsen M, Bayer A, Sydnes MO, Jørgensen KB. Tetrahedron 2015, 8278. Total synthesis of tubastrine and 3-dehydroxy tubastrine by microwave-assisted cross-coupling reactions.  doi: 10.1016/j.tet.2015.09.003 UiT´s open research archive

22. Demissie TB, Kostenko N, Komorovsky S, Repisky M, Isaksson J, Bayer A*, Ruud K. J. Phys. Org. Chem. 2015, 723. Experimental and Four-Component Relativistic DFT Studies of Tungsten Carbonyl Complexes. Article highlighted on the cover page.  UiT´s open research archive

21. Pandey S, Guttormsen Y, Haug BE, Hedberg C, Bayer A*. Org. Lett. 2015, 122. A Concise Total Synthesis of Breitfussin A and B. Open access! doi: 10.1021/ol503348n

20. Hopmann KH, Frediani L, Bayer A. Organometallics 2014, 2790. Iridium-PHOX-mediated alkene hydrogenation: Isomerisation influences the stereochemical outcome. doi: 10.1021/om5002843 UiT´s fulltext archive

19. Hopmann KH, Bayer A*. Coord. Chem. Rev. 2014, 59. Enantioselective Imine Hydrogenation with Iridium-Catalysts: Reactions, Mechanisms, and Stereocontrol.

18. Lind KF, Hansen E, Østerud B, Eilertsen KE, Bayer A, Engqvist M, Leszczak K, Jørgensen TØ, Jeanette H. Andersen JH. Marine Drugs. 2013, 2655. Antioxidant and anti-inflammatory activities of barettin. Open access! doi: 10.3390/md11072655

17. Kostenko N, Ericsson C, Engqvist M, Villa Gonzalez S, Bayer A*. Eur. J. Org. Chem. 2013, 4756. Palladium(0)-Catalysed Cross-Couplings of 2-Bromophosphinine. UiT´s fulltext archive

16. Melnes, S, Bayer A, Gautun OR. Tetrahedron 2013, 7910. Aryl MIDA boronates from cyclotrimerization of ethynyl MIDA boronate with diynes.

15. Melnes, S, Bayer A, Gautun OR. Tetrahedron 2012, 8463. Cyclotrimerization of unsymmetrically bromo-substituted diynes: Towards the synthesis of potential selective inhibitors of tyrosine kinase 2.

14. Hopmann KH, Bayer A. Organometallics 2011, 2483 On the Mechanism of Iridium-Catalyzed Asymmetric Hydrogenation of Imines and Alkenes: A Theoretical Study

13. Endeshaw MM, Bayer A, Hansen LK, Gautun OR. Eur. J. Org. Chem. 2006, 5249–5259. Catalytic Asymmetric Hetero Diels-Alder Reactions of N-Sulfinyl Dienophiles with Chiral Bis(oxazoline)copper(II) and -zinc(II) Triflates.

12. Bayer A. Dihydroxylation of Carbon-Carbon Double Bonds. In Comprehensive Asymmetric Catalysis. Supplement 2. 2004 Jacobsen EN, Pfaltz A, Yamamoto H. (Eds), Springer Verlag

11. Bayer A. Aminohydroxylation of Carbon-Carbon Double Bonds. In Comprehensive Asymmetric Catalysis. Supplement 2. 2004 Jacobsen EN, Pfaltz A, Yamamoto H. (Eds), Springer Verlag

10. Källström K, Hedberg C, Brandt P, Bayer A, Andersson PG. J. Am. Chem. Soc. 2004 14308-14309 Rationally Designed Ligands for Asymmetric Iridium Catalyzed Hydrogenation of Olefins.

9. Bayer A, Endeshaw MM, Gautun OR. J. Org. Chem. 2004, 7198-7205. Asymmetric Hetero Diels-Alder Reactions of N-Sulfinyl Dienophiles Using Chiral Bis(oxazoline)–Copper(II) or –Zinc(II) Triflates.

8. Bayer A, Hansen LK, Gautun OR. Tetrahedron: Asymmetry 2002, 13, 2407-2415. Asymmetric Diels-Alder reactions of N-sulfinyl dienophiles using chiral Ti(IV) Lewis acids.

7. Hansen LK, Bayer A, Gautun OR. Acta Cryst. 2002, E58, o198–o199. (1R*,3R*,6S*)-3,6-Dihydro-3,6-dimethyl-2-(toluene-4-sulfonyl)-1λ4,2-thiazine 1-oxide.

6. Hansen LK, Bayer A, Gautun OR. Acta Cryst. 2002, E58, o165–o166. Benzyl (1R*,3S*)-3,6-dihydro-3-methyl-1λ4,2-thiazine-2-carboxylate 1-oxide.

5. Bayer A, Svendsen JS. Eur. J. Org. Chem. 2001, 1769-1780. Substrate Binding in the Asymmetric Dihydroxylation Reaction – Investigation of the Stereoselectivity in the Dihydroxylation of Cs-Symmetric Divinylcarbinol Derivatives.

4. Hansen LK, Bayer A, Gautun OR. Acta Cryst. 2001, E57, o1109-o1110. exo-2-benzoyloxycarbonyl-3,6-dihydro-3-methyl-1λ4,2-thiazine 1-oxide.

3. Bayer A, Gautun OR. Tetrahedron: Asymmetry 2001, 12, 2937-2939. Highly enantioselective hetero Diels-Alder reactions of N-sulfinyl dienophiles promoted by chiral copper(II)- or zinc(II)-bis(oxazoline) complexes.

2. Bayer A, Gautun OR. Tetrahedron Lett. 2000, 41, 3743-3746. Asymmetric N-sulfinyl dienophile Diels-Alder cycloadditions using chiral Ti(IV)-based Lewis Acids.

1. Henderson RJ, Burkow IC, Buzzi M, Bayer A. Biochem. Biophys Acta 1998, 1392, 309-319. Effects of docosahexaenoic (22:6n-3), tetracosapentaenoic (24:5n-3) and tetracosahexaneoic (24:6n-3) acids on the elongation of n-3 polyunsaturated fatty acids in trout liver microsomes.