{"id":63,"date":"2017-05-23T11:45:43","date_gmt":"2017-05-23T09:45:43","guid":{"rendered":"https:\/\/site.uit.no\/bayerlab\/?page_id=63"},"modified":"2026-04-16T21:13:37","modified_gmt":"2026-04-16T19:13:37","slug":"publications","status":"publish","type":"page","link":"https:\/\/site.uit.no\/bayerlab\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n
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\n66. Langer MK, Bayer A. J. Org. Chem., 2025, 13597. Stereocontrolled and Adaptable Synthesis of (\u2013)-Aspergilone A via the Key Intermediate (+)-Phenol A. Open access! doi: 10.1021\/acs.joc.5c01650\n\n\n\n
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65. Singh M, Boomgaren M, Bakht P, Ihle P, Leiros HKS, Bayer A, Pathania R. J. Med. Chem., 2025<\/strong>, 13421. Design and SAR Analysis of Phenylboronic Acid-Based Inhibitors for Sensitizing KPC-2-Producing Klebsiella pneumoniae to \u03b2-Lactam Antibiotics<\/em>. (IF 6.8) doi: 10.1021\/acs.jmedchem.5c00058<\/a><\/p>\n\n\n\n

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64. Reierth IAN, Guttormsen Y, Andersen JH, Hansen EH, Abdelhady AM, Langer MK, Haug BE, Bayer A, Petit GA. Bioorg. Med. Chem., 2025<\/b>, 118489. <\/span>Investigation of the histone deacetylase inhibitor potential of phorbazole analogues<\/span><\/i>. doi: <\/span>10.1016\/j.bmc.2025.118489<\/a><\/span><\/p>\n

63. Pettersen M, Do CD, Obst MF, Damm R, Putra AE, Manoij S, Gevorgyan A, Pavlovic L, Hopmann KH,\u00a0<\/span>Bayer A<\/span>.<\/span>\u00a0<\/span><\/span>Adv. Synth. Catal.<\/span>, 2024<\/b>, <\/span>2976. <\/span>A<\/i>symmetric boracarboxylation of styrenes using carbon dioxide<\/span><\/i>. Open access!<\/strong><\/span> <\/span><\/i>doi: 10.1002\/adsc.202301285<\/a><\/span><\/p>\n

62. Kondratieva A, Palica K, Fr\u00f8hlich C, Hovd RR, Leiros HKS, Erdelyi M, <\/span>Bayer A. <\/span><\/span>Eu. J. Med. Chem., 2024<\/b>, accepted. <\/span>Fluorinated Captopril Analogues Inhibit Metallo-<\/span>\u00df<\/span>-Lactamases and Facilitate Structure Determination of NDM-1 <\/span>Binding Pose<\/span>. Open access!<\/strong><\/span> doi: 10.1016\/j.ejmech.2024.116140<\/a><\/span><\/span><\/i>\"\"<\/p>\n<\/div>\n

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61. <\/span>Langer MK, Rahman A, Dey H, Andersen T, Haug T, Blencke HM, Stensv\u00e5g K, Str\u00f8m MB, Bayer A. Eu. J. Med. <\/span>Chem., <\/span>2023<\/span><\/b>,<\/span> 115147<\/span>. Investigation of Tetrasubstituted Heterocycles Reveals Hydantoins as a Promising Scaffold for Development of Novel Antimicrobials with Membranolytic Properties<\/i>. Open access!<\/strong><\/span> doi: 10.1016\/j.ejmech.2023.115147<\/span><\/a><\/span><\/p>\n<\/div>\n

60.<\/span>\u00a0Sousa<\/span><\/span>\u00a0<\/span><\/span>A,\u00a0<\/span><\/span>Bor\u00f8y<\/span><\/span> V<\/span><\/span>,\u00a0<\/span><\/span>B\u00e6verud<\/span><\/span> A<\/span><\/span>,\u00a0<\/span><\/span>Julin<\/span><\/span> K<\/span><\/span>,\u00a0<\/span><\/span>Bayer A<\/span><\/span>,\u00a0<\/span><\/span>Str\u00f8m<\/span><\/span> M,\u00a0<\/span><\/span>Johannessen<\/span><\/span> M,\u00a0<\/span><\/span>\u0160kalko-Basnet<\/span><\/span> N, <\/span><\/span>Obuobi S.<\/span><\/span>\u00a0<\/span><\/span> J. Mater. Chem. B<\/span>, 2023<\/b>, <\/span>7972. <\/span>Polymyxin B stabilized DNA micelles for sustained antibacterial and antibiofilm activity against P. aeruginosa<\/span><\/i>. Open access!<\/strong><\/span><\/span><\/i>\u00a0doi: 10.1039\/D3TB00704A<\/a>\u00a0<\/span><\/p>\n<\/div>\n

59. Hemmingsen LM, Giordani B, Paulsen MH, Vanic Z, Flaten GE, Vitali B, Basnet P, Bayer A, Str\u00f8m MB, Skalko-Basnet N. Biomat. Adv. 2023<\/b>, <\/span>213238<\/span>. \u00a0<\/span>Tailored anti-biofilm activity \u2013 liposomal delivery for mimic of small antimicrobial peptide. Open access!<\/strong><\/span> <\/span><\/span><\/i>doi: 10.1016\/j.bioadv.2022.213238<\/span><\/a><\/span><\/p>\n

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58. <\/span>von Hofsten<\/span> S, Langer M, Korelin K, Magnussen S, <\/span>Ausbacher D, <\/span>Andersen T, Salo T, <\/span>Str\u00f8m MB, <\/span>Bayer A<\/span>, Berge G. <\/span>Front. Pharmacol. 2023<\/b>, <\/span>Amphipathic barbiturates as marine product mimics with cytolytic and immunogenic effects on head and neck squamous cell carcinoma cell lines<\/span><\/i>. Open access!<\/strong><\/span>\u00a0<\/span>doi: <\/span>10.3389\/fphar.2023.1141669<\/span><\/a><\/p>\n<\/div>\n<\/div>\n

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57. von Hofsten S, Paulsen MH, Magnussen SN, Ausbacher D, Kranz M, Bayer A, Str\u00f8m MB, Berge G. Sci. Rep., 2022<\/strong>, 15586. The marine natural product mimic MPM-1 is cytolytic and induces DAMP release from human cancer cell lines<\/em>. Open access!<\/strong><\/span> doi: 10.1038\/s41598-022-19597-4<\/span><\/a><\/p>\n

56. Langer MK, Rahman A, Dey H, Andersen T, Zilioli F, Haug T, Blencke HM, Stensv\u00e5g K, Str\u00f8m MB, Bayer A. Eu. J. Med. Chem., 2022<\/strong>, 114632. A concise SAR-analysis of antimicrobial cationic amphipathic barbiturates for an improved activity-toxicity profile<\/em>. Open access!<\/strong><\/span> doi: 10.1016\/j.ejmech.2022.114632<\/a><\/p>\n

55. Wieske LHE, Bogaerts J, Leding AAM, Wilcox S, Rasmussen AA, Leszczak K, Turunen L, Herrebout WA, Hubert M, Bayer A, Erd\u00e9lyi M. ACS Med. Chem. Lett., 2022<\/strong>, 257-61. NMR Backbone Assignment of VIM-2 and Identification of the Active Enantiomer of a Potential Inhibitor<\/em>. Open access!<\/span><\/strong> doi: 10.1021\/acsmedchemlett.1c00635<\/a><\/p>\n

54. Gevorgyan A, Hopmann HK, Bayer A. Organometallics, 2022<\/strong>, 1777-85. Improved Buchwald\u2013Hartwig Amination by the Use of Lipids and Lipid Impurities<\/em>.\u00a0Open access!<\/strong><\/span> doi: 10.1021\/acs.organomet.1c00517<\/a>.<\/p>\n

53. Gevorgyan A, Hopmann HK, Bayer A. Green Chemistry, 2021<\/strong>, 7219-27. Lipids as Versatile Solvents for Chemical Synthesis. <\/em>UiT\u00b4s open research archive<\/span><\/strong>;<\/em> doi: 10.1039\/D1GC02311J<\/a>.<\/p>\n

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, Str\u00f8m MB. J. Med. Chem., 2021<\/strong>,11395<\/span>. Amphipathic Barbiturates as Mimics of Antimicrobial Peptides and the Marine Natural Products Eusynstyelamides with Activity Against Multi-Resistant Clinical Isolates<\/em>. Open access! <\/strong> <\/em><\/span>doi: 10.1021\/acs.jmedchem.1c00734<\/a>.<\/p>\n

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\"\"51. Pavlovic L, Pettersen M, Gevorgyan A, Vaitla J, Bayer A, Hopmann HK. Eur. J. Org. Chem., 2021<\/strong>, 663.<\/em> Computational and experimental insights into asymmetric Rh-catalyzed hydrocarboxylation with CO2<\/sub>.<\/em> Open access! <\/strong> <\/em><\/span>doi: 10.1002\/ejoc.202001469.<\/a><\/p>\n

50. Guttormsen Y, Fairhorst M, Pandey SK, Isaksson J, Haug BE, Bayer A. Molecules, 2020<\/strong>, 4848. Total synthesis of Phorbazole B. Open access! <\/strong><\/span> doi: 10.3390\/molecules25204848<\/a>.
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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<\/strong>, 12081. Unequivocal Structure Confirmation of a Breitfussin Analog by Anisotropic NMR Measurements.<\/em> Open access! <\/strong> <\/span>doi: 10.1039\/D0SC03664A<\/a>.<\/p>\n

48. Ismael A, Gevorgyan A, Skrydstrup T, Bayer, A. Org. Process Res. Dev., 2020<\/strong>, 2665<\/span>. Renewable Solvents for Palladium-Catalyzed Carbonylation Reactions<\/em>.\u00a0Open access! <\/strong><\/span> doi: 10.1021\/acs.oprd.0c00325<\/a>.<\/p>\n

47. Muhammad Z, Skagseth S, Akhter S, Fr\u00f6hlich C, Christopheit T, Bayer A, Leiros HKS. Bioorg. Med. Chem., 2020<\/strong>, 115598. Structural studies of<\/em> triazole inhibitors with promising inhibitor effects against antibiotic resistance metallo-<\/em>\u03b2-lactamases. <\/em>Open access!<\/span> <\/strong>doi: 10.1016\/j.bmc.2020.115598<\/a>.
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46. Samuelsen \u00d8, \u00c5strand OAH, Fr\u00f6hlich C, Heikal A, Skagseth S, Carlsen TJO, Leiros HKS, Bayer A, Schnaars C, Kildahl-Andersen G, Lauksund S, Finke S, Huber S, Gj\u00f8en T, Andresen AMS, \u00d8kstad OA, Rongved P. Antimicrob. Chemother. Agents , 2020<\/strong>, e02415.\u00a0ZN148\u2013a modular synthetic metallo-\u03b2-lactamase inhibitor reverses carbapenem-resistance in Gram-negative pathogens in vivo.<\/em>\u00a0Open access!<\/span><\/strong> doi: 10.1128\/AAC.02415-19<\/a>.<\/p>\n

45. Ismael A, Skrydstrup T, Bayer A. Org. Bioorg. Chem., 2020<\/strong>, 1754. Carbonylative Suzuki-Miyaura couplings of sterically hindered aryl halides: Synthesis of 2-aroylbenzoate derivatives<\/em>. UiT\u00b4s open research archive<\/a><\/span><\/strong>; doi: 10.1039\/D0OB00044B<\/a>.<\/p>\n

44. Gevorgyan A, Hopmann HK, Bayer A. Chem. Eur. J. 2020<\/strong>, 6064. Formal C-H carboxylation of unactivated arenes with carbon dioxide.\u00a0<\/em>Open access!<\/span> <\/strong>doi: 10.1002\/chem.202000515<\/a>. Featured in Org. Chem. Highlights 12th oct. 2020: Substituted Benzenes!<\/a><\/span><\/strong><\/p>\n

43. Gevorgyan A, Hopmann HK, Bayer A. ChemSusChem, 2020<\/strong>, 2080. Exploration of New Biomass-Derived Solvents: Application to Carboxylation Reactions. Open access!<\/span><\/strong> doi:10.1002\/cssc.201903224<\/a>.
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42. Obst M, Gevorgyan A, Bayer A, Hopmann HK. Organometallics, 2020<\/strong>, 1545. Mechanistic insights into copper-catalysed carboxylations<\/em>. UiT\u00b4s open research archive<\/span><\/strong>; doi:10.1021\/acs.organomet.9b00710<\/a>.<\/p>\n

41.\u00a0Hansen K, Andersen J, Bayer A, Pandey S, Lorentzen M, J\u00f8rgensen K, Sydnes M, Guttormsen Y, Baumann M, Klebl B, Eickhoff J, Haug B, Isaksson J, Hansen E.\u00a0J. Med. Chem. 2019<\/strong>, 10167<\/span>.\u00a0Kinase Chemodiversity from the Arctic: The Breitfussins.\u00a0<\/em>UiT\u00b4s open research archive<\/a><\/strong><\/span>; doi: 10.1021\/acs.jmedchem.9b01006<\/a>.<\/em><\/p>\n

40. Gevorgyan A, Obst M, Maseras F, Hopmann HK, Bayer A. Chem. Sci. 2019<\/strong>, 10072. Caesium-Fluoride Mediated Hydrocarboxylation of Alkenes and Allenes: Scope and Mechanistic Insight. Open access!<\/span><\/strong> doi: 10.1039\/c9sc02467k<\/a>.
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39. Paulsen MH, Ausbacher D, Bayer A, Engqvist M, Hansen T, Haug T, Anderssen T, Anderssen JH, Sollid JUE, Str\u00f8m MB. Eur. J. Med.\u00a0Chem. 2019<\/strong>, 111671. Antimicrobial activity of amphipathic \u03b1,\u03b1-disubstituted \u03b2-amino amide derivatives against ESBL \u2013 CARBA producing multi-resistant bacteria; effect of halogenation, lipophilicity and cationic character. Open access!<\/span> <\/strong>doi: 10.1016\/j.ejmech.2019.111671<\/a>.
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38. Vaitla J, Bayer A, Hopmann KH. Synlett. 2019<\/strong>, 1377. Vinyl Sulfoxonium Ylide: A New Vinyl Carbenoid Transfer Reagent for the Synthesis of Heterocycles. UiT\u00b4s open research archive<\/span><\/strong>;<\/em> doi: 10.1055\/s-0037-1611771<\/a>.<\/p>\n

37. Vaitla J, Bayer A. Synthesis 2019<\/strong>, 612. Sulfoxonium ylide derived metal carbenoids in organic synthesis.\u00a0UiT\u00b4s open research archive<\/a><\/span><\/strong>;<\/em> doi: 10.1055\/s-0037-1610328.<\/a><\/p>\n

36. Vaitla J, Bayer A, Hopmann KH. Ang. Chem. Int. Ed. 2018<\/strong>, 16180. Iron\u2010Catalyzed Carbenoid Transfer Reactions of Vinyl Sulfoxonium Ylides: An Experimental and Computational Study.\u00a0<\/em>UiT\u00b4s open research archive<\/span><\/strong><\/a>;<\/em> doi: 10.1002\/anie.201810451<\/a>.<\/p>\n

35. Paulsen MH, Karlsen EA, Ausbacher D, Andersen T, Bayer A, Ochtrop P, Hedberg C, Haug T, Sollid JUE, Str\u00f8m MB. J. Pep. Sci. 2018<\/strong>, 24<\/span>:e3117. An amphipathic cyclic tetrapeptide scaffold containing halogenated \u03b2 2,2<\/sup>-amino acids with activity against multi-resistant bacteria<\/em>. doi: 10.1002\/psc.3117<\/a>.<\/p>\n

34. Pavlovic L, Vaitla J, Bayer A, Hopmann KH. Organometallics 2018<\/strong>, 941. Rhodium-Catalyzed Hydrocarboxylation: Mechanistic Analysis Reveals Unusual Transition State for Carbon-Carbon Bond Formation<\/em>. UiT\u00b4s open research archive<\/span><\/strong><\/span><\/a>; doi: 10.1021\/acs.organomet.7b00899<\/a>.<\/p>\n

33. Fairhurst M, Zeeshan M, Haug BE, Bayer A. Synlett 2018<\/strong>, 1303. Aldol condensations on a 3-alkylidene-2,5-diketopiperazine –\u00a0 synthesis of two marine natural products. <\/em>UiT\u00b4s open research archive<\/span><\/strong><\/a><\/span>;\u00a0doi: 10.1055\/s-0036-1591755<\/a><\/p>\n

32. Akhter S, Lund BA, Ismael A, Lange M, Christopeit T, Leiros HKS, Bayer A. Eur. J. Med. Chem. 2018<\/strong>, 634. A focused fragment library targeting the antibiotic resistance enzyme – Oxacillinase-48: synthesis, structural evaluation and inhibitor design. <\/em>UiT\u00b4s open research archive<\/span><\/strong><\/span><\/a>; doi: 10.1016\/j.ejmech.2017.12.085<\/a><\/p>\n

31.\u00a0Hansen K, Isaksson J, Bayer A, Johansen J, Andersen JH, Hansen E. J. Nat. Prod. 2017<\/strong>, 3276. Securamine Derivatives from the Arctic Bryozoan Securiflustra securifrons. doi: 10.1021\/acs.jnatprod.7b00703<\/a><\/em><\/p>\n

30. Vaitla J, Hopmann KH, Bayer A. Org. Lett. 2017<\/strong>, 6688. Rhodium-Catalyzed Synthesis of Sulfur Ylides via in Situ Generated Iodonium Ylides. <\/em>UiT\u00b4s open research arc<\/span>hive<\/span><\/a><\/strong>; doi: 10.1021\/acs.orglett.7b03413<\/a><\/p>\n

29. Vaitla J, Guttormsen Y, Mannisto JK, Nova A, Repo T, Bayer A, Hopmann KH. ACS Catalysis 2017<\/strong>, 7231. Enantioselective Incorporation of CO2<\/sub>: Status and Potential.<\/em> UiT\u00b4s open research archive<\/a><\/span><\/strong>; doi: 10.1021\/acscatal.7b02306<\/a><\/p>\n

28. Skagseth S, Christopeit T, Akhter S, Bayer A, Samuelsen \u00d8, Leiros HKS. Antimicrob. Chemother. Agents 61, 2017<\/strong>, e02602. Structural insights into TMB-1 and the role of residue 119 and 228 in substrate and inhibitor activity. <\/em>UiT\u00b4s open research archive<\/span><\/strong><\/a><\/span>; doi: 10.1128\/AAC.02602-16<\/a><\/p>\n

27. Vaitla J, Bayer A, Hopmann KH. Ang. Chem. Int. Ed. 2017<\/strong>, 4277. Synthesis of Indoles and Pyrroles Utilizing Iridium Carbenes Generated from Sulfoxonium Ylides<\/em>. UiT\u00b4s open research archive<\/a><\/strong><\/span>; doi:10.1002\/anie.201610520<\/a>. Featured in Org. Chem. Highlights 16th Oct 2017: Heterocycle construction!<\/span><\/strong><\/span><\/a><\/span><\/p>\n

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26. Skagseth S, Akhter S, Paulsen MH, Muhammad Z, Samuelsen \u00d8, Leiros HKS, Bayer A. Eur. J. Med.Chem. 135<\/em>, 2017<\/strong>, 159. Metallo-\u03b2-lactamase inhibitors by bioisosteric replacement: preparation, activity and binding. <\/em>UiT\u00b4s open research archive<\/span><\/a><\/strong>; doi: 10.1016\/j.ejmech.2017.04.035<\/a><\/p>\n

25. Paulsen MH, Engqvist M, D. Ausbacher, Str\u00f8m MB, Bayer A. Org. Biomol. Chem. 2016<\/strong>, 7570. Efficient and scalable synthesis of \u03b1,\u03b1-disubstituted \u03b2\u2013amino amides. Open access! <\/span><\/strong><\/em>doi:\u00a0<\/strong>10.1039\/C6OB01219A<\/a><\/p>\n

24. Lund BA, Guttormsen Y, Christopeit T, Bayer A, Leiros HKS. J. Med. Chem. 2016<\/strong>, 5542. Screening and Design of Inhibitor Scaffolds for the Antibiotic Resistance Oxacillinase-48 (OXA-48) through Surface Plasmon Resonance Screening.<\/em> UiT\u00b4s open research archive<\/a><\/strong><\/span>; doi: 10.1021\/acs.jmedchem.6b00660<\/a>.<\/em><\/p>\n

23. Lorentsen M, Bayer A, Sydnes MO, J\u00f8rgensen KB. Tetrahedron 2015<\/strong>, 8278. Total synthesis of tubastrine and 3-dehydroxy tubastrine by microwave-assisted cross-coupling reactions.\u00a0<\/em> doi:\u00a010.1016\/j.tet.2015.09.003<\/a><\/em>\u00a0UiT\u00b4s open research arch<\/span><\/strong><\/span><\/a><\/span>ive<\/span><\/strong><\/p>\n

22. Demissie TB, Kostenko N, Komorovsky S, Repisky M, Isaksson J, Bayer A*, Ruud K. J. Phys. Org. Chem. 2015<\/strong>, 723. Experimental and Four-Component Relativistic DFT Studies of Tungsten Carbonyl Complexes. <\/em>Article highlighted on the cover page. \u00a0UiT\u00b4s open research arch<\/span><\/strong><\/span><\/a>iv<\/span>e<\/strong><\/span>
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21. Pandey S, Guttormsen Y, Haug BE, Hedberg C, Bayer A*. Org. Lett. 2015<\/strong>, 122. A Concise Total Synthesis of Breitfussin A and B. Open access!<\/span><\/strong> doi:\u00a010.1021\/ol503348n<\/a><\/em><\/p>\n

20. Hopmann KH, Frediani L, Bayer A. Organometallics 2014<\/strong>, 2790. Iridium-PHOX-mediated alkene hydrogenation: Isomerisation influences the stereochemical outcome<\/em>. doi:\u00a010.1021\/om5002843<\/a>\u00a0UiT\u00b4s fulltext arch<\/span><\/strong><\/a>ive<\/span><\/strong><\/p>\n

19. Hopmann KH, Bayer A*. Coord. Chem. Rev. 2014<\/strong>, 59. Enantioselective Imine Hydrogenation with Iridium-Catalysts: Reactions, Mechanisms, and Stereocontrol<\/em>.<\/p>\n

18. Lind KF, Hansen E, \u00d8sterud B, Eilertsen KE, Bayer A, Engqvist M, Leszczak K, J\u00f8rgensen T\u00d8, Jeanette H. Andersen JH. Marine Drugs. 2013<\/strong>, 2655. Antioxidant and anti-inflammatory activities of barettin. Open access!<\/span><\/strong> doi:\u00a010.3390\/md11072655<\/a><\/em><\/p>\n

17. Kostenko N, Ericsson C, Engqvist M, Villa Gonzalez S, Bayer A*. Eur. J. Org. Chem. 2013<\/strong>, 4756. Palladium(0)-Catalysed Cross-Couplings of 2-Bromophosphinine. <\/em>UiT\u00b4s fulltext archive<\/span><\/strong><\/a><\/span>
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16. Melnes, S, Bayer A, Gautun OR. Tetrahedron 2013<\/strong>, 7910. Aryl MIDA boronates from cyclotrimerization of ethynyl MIDA boronate with diynes.<\/p>\n

15. Melnes, S, Bayer A, Gautun OR. Tetrahedron 2012<\/strong>, 8463. Cyclotrimerization of unsymmetrically bromo-substituted diynes: Towards the synthesis of potential selective inhibitors of tyrosine kinase 2<\/em>.<\/p>\n

14. Hopmann KH, Bayer A. Organometallics 2011<\/strong>, 2483 On the Mechanism of Iridium-Catalyzed Asymmetric Hydrogenation of Imines and Alkenes: A Theoretical Study<\/p>\n

13. Endeshaw MM, Bayer A, Hansen LK, Gautun OR. Eur. J. Org. Chem. 2006<\/strong>, 5249\u20135259. Catalytic Asymmetric Hetero Diels-Alder Reactions of N-Sulfinyl Dienophiles with Chiral Bis(oxazoline)copper(II) and -zinc(II) Triflates.<\/em><\/p>\n

12. Bayer A. Dihydroxylation of Carbon-Carbon Double Bonds<\/em>. In Comprehensive Asymmetric Catalysis. Supplement 2. 2004<\/strong> Jacobsen EN, Pfaltz A, Yamamoto H. (Eds), Springer Verlag<\/p>\n

11. Bayer A. Aminohydroxylation of Carbon-Carbon Double Bonds.<\/em> In Comprehensive Asymmetric Catalysis. Supplement 2. 2004<\/strong> Jacobsen EN, Pfaltz A, Yamamoto H. (Eds), Springer Verlag<\/p>\n

10. K\u00e4llstr\u00f6m K, Hedberg C, Brandt P, Bayer A, Andersson PG. J. Am. Chem. Soc. 2004<\/strong> 14308-14309 Rationally Designed Ligands for Asymmetric Iridium Catalyzed Hydrogenation of Olefins.<\/em><\/p>\n

9. Bayer A, Endeshaw MM, Gautun OR. J. Org. Chem. 2004<\/strong>, 7198-7205. Asymmetric Hetero Diels-Alder Reactions of N-Sulfinyl Dienophiles Using Chiral Bis(oxazoline)\u2013Copper(II) or \u2013Zinc(II) Triflates.<\/em><\/p>\n

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

7. Hansen LK, Bayer A, Gautun OR. Acta Cryst. 2002<\/strong>, E58<\/em>, o198\u2013o199. (1R*,3R*,6S*)-3,6-Dihydro-3,6-dimethyl-2-(toluene-4-sulfonyl)-1\u03bb<\/em>4<\/sup><\/em>,2-thiazine 1-oxide.<\/em><\/p>\n

6. Hansen LK, Bayer A, Gautun OR. Acta Cryst. 2002<\/strong>, E58<\/em>, o165\u2013o166. Benzyl (1R*,3S*)-3,6-dihydro-3-methyl-1\u03bb4<\/sup>,2-thiazine-2-carboxylate 1-oxide<\/em>.<\/em><\/p>\n

5. Bayer A, Svendsen JS. Eur. J. Org. Chem. 2001<\/strong>, 1769-1780. Substrate Binding in the Asymmetric Dihydroxylation Reaction \u2013 Investigation of the Stereoselectivity in the Dihydroxylation of Cs<\/sub>-Symmetric Divinylcarbinol Derivatives.<\/em><\/p>\n

4. Hansen LK, Bayer A, Gautun OR. Acta Cryst. 2001<\/strong>, E57<\/em>, o1109-o1110. exo-2-benzoyloxycarbonyl-3,6-dihydro-3-methyl-1\u03bb4<\/sup>,2-thiazine 1-oxide<\/em>.<\/p>\n

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

2. Bayer A, Gautun OR. Tetrahedron Lett. 2000<\/strong>, 41<\/em>, 3743-3746. Asymmetric N-sulfinyl dienophile Diels-Alder cycloadditions using chiral Ti(IV)-based Lewis Acids.<\/em><\/p>\n

1. Henderson RJ, Burkow IC, Buzzi M, Bayer A. Biochem. Biophys Acta 1998<\/strong>, 1392<\/em>, 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<\/em>.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n

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66. Langer MK, Bayer A. J. Org. Chem., 2025, 13597. Stereocontrolled and Adaptable Synthesis of (\u2013)-Aspergilone A via the Key Intermediate (+)-Phenol A. Open access! doi: 10.1021\/acs.joc.5c01650 65. Singh M, Boomgaren M, Bakht P, Ihle P, Leiros HKS, Bayer A, … Continue reading →<\/span><\/a><\/p>\n","protected":false},"author":826,"featured_media":221,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-63","page","type-page","status-publish","has-post-thumbnail","hentry"],"_links":{"self":[{"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/pages\/63","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/users\/826"}],"replies":[{"embeddable":true,"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/comments?post=63"}],"version-history":[{"count":4,"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/pages\/63\/revisions"}],"predecessor-version":[{"id":759,"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/pages\/63\/revisions\/759"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/media\/221"}],"wp:attachment":[{"href":"https:\/\/site.uit.no\/bayerlab\/wp-json\/wp\/v2\/media?parent=63"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}