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Annette Bayer - Publications

Affiliations: 
University of Tromsø – The Arctic University of Norway 
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31 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Ismael A, Skrydstrup T, Bayer A. Carbonylative Suzuki-Miyaura couplings of sterically hindered aryl halides: synthesis of 2-aroylbenzoate derivatives. Organic & Biomolecular Chemistry. PMID 32065204 DOI: 10.1039/D0Ob00044B  0.478
2020 Gevorgyan A, Hopmann KH, Bayer A. Formal C-H Carboxylation of Unactivated Arenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32003869 DOI: 10.1002/Chem.202000515  0.668
2020 Gevorgyan A, Hopmann KH, Bayer A. Exploration of New Biomass-Derived Solvents: Application to Carboxylation Reactions. Chemsuschem. PMID 31909560 DOI: 10.1002/Cssc.201903224  0.738
2020 Obst MF, Gevorgyan A, Bayer A, Hopmann KH. Mechanistic Insights into Copper-Catalyzed Carboxylations Organometallics. 39: 1545-1552. DOI: 10.1021/Acs.Organomet.9B00710  0.658
2020 Ismael A, Gevorgyan A, Skrydstrup T, Bayer A. Renewable Solvents for Palladium-Catalyzed Carbonylation Reactions Organic Process Research & Development. 24: 2665-2675. DOI: 10.1021/Acs.Oprd.0C00325  0.43
2019 Gevorgyan A, Obst MF, Guttormsen Y, Maseras F, Hopmann KH, Bayer A. Caesium fluoride-mediated hydrocarboxylation of alkenes and allenes: scope and mechanistic insights. Chemical Science. 10: 10072-10078. PMID 32055361 DOI: 10.1039/C9Sc02467K  0.731
2019 Vaitla J, Bayer A, Hopmann KH. Vinyl Sulfoxonium Ylide: A New Vinyl Carbenoid Transfer Reagent for the Synthesis of Heterocycles Synlett. 30: 1377-1383. DOI: 10.1055/S-0037-1611771  0.784
2019 Vaitla J, Bayer A. Sulfoxonium Ylide Derived Metal Carbenoids in Organic Synthesis Synthesis. 51: 612-628. DOI: 10.1055/S-0037-1610328  0.772
2018 Vaitla J, Bayer A, Hopmann KH. Iron-Catalyzed Carbenoid-Transfer Reactions of Vinyl Sulfoxonium Ylides: An Experimental and Computational Study. Angewandte Chemie (International Ed. in English). PMID 30318836 DOI: 10.1002/Anie.201810451  0.773
2018 Paulsen MH, Karlsen EA, Ausbacher D, Anderssen T, Bayer A, Ochtrop P, Hedberg C, Haug T, Sollid JUE, Strøm MB. An amphipathic cyclic tetrapeptide scaffold containing halogenated β2,2‐amino acids with activity against multiresistant bacteria Journal of Peptide Science. 24. PMID 30112781 DOI: 10.1002/Psc.3117  0.319
2018 Fairhurst ME, Zeeshan M, Haug BE, Bayer A. Aldol Condensations on a 3-Alkylidene-2,5-diketopiperazine: Synthesis of Two Marine Natural Products Synlett. 29: 1303-1306. DOI: 10.1055/S-0036-1591755  0.36
2018 Pavlovic L, Vaitla J, Bayer A, Hopmann KH. Rhodium-Catalyzed Hydrocarboxylation: Mechanistic Analysis Reveals Unusual Transition State for Carbon–Carbon Bond Formation Organometallics. 37: 941-948. DOI: 10.1021/Acs.Organomet.7B00899  0.755
2017 Vaitla J, Hopmann KH, Bayer A. Rhodium-Catalyzed Synthesis of Sulfur Ylides via in Situ Generated Iodonium Ylides. Organic Letters. PMID 29166023 DOI: 10.1021/Acs.Orglett.7B03413  0.779
2017 Vaitla J, Bayer A, Hopmann KH. Synthesis of Indoles and Pyrroles Utilizing Iridium Carbenes Generated from Sulfoxonium Ylides. Angewandte Chemie (International Ed. in English). PMID 28319303 DOI: 10.1002/Anie.201610520  0.777
2017 Vaitla J, Guttormsen Y, Mannisto JK, Nova A, Repo T, Bayer A, Hopmann KH. Enantioselective Incorporation of CO2: Status and Potential Acs Catalysis. 7: 7231-7244. DOI: 10.1021/Acscatal.7B02306  0.754
2016 Paulsen MH, Engqvist M, Ausbacher D, Strøm MB, Bayer A. Efficient and scalable synthesis of α,α-disubstituted β-amino amides. Organic & Biomolecular Chemistry. 14: 7570-8. PMID 27439743 DOI: 10.1039/C6Ob01219A  0.41
2015 Pandey SK, Guttormsen Y, Haug BE, Hedberg C, Bayer A. A Concise Total Synthesis of Breitfussin A and B Organic Letters. 17: 122-125. PMID 25514017 DOI: 10.1021/Ol503348N  0.317
2015 Lorentzen M, Bayer A, Sydnes MO, Jørgensen KB. Total synthesis of tubastrine and 3-dehydroxy tubastrine by microwave-assisted cross-coupling reactions Tetrahedron. 71: 8278-8284. DOI: 10.1016/J.Tet.2015.09.003  0.358
2015 Hopmann KH, Bayer A. ChemInform Abstract: Enantioselective Imine Hydrogenation with Iridium-Catalysts: Reactions, Mechanisms and Stereocontrol Cheminform. 46: no-no. DOI: 10.1002/CHIN.201524266  0.678
2014 Hopmann KH, Frediani L, Bayer A. Iridium-PHOX-mediated alkene hydrogenation: Isomerization influences the stereochemical outcome Organometallics. 33: 2790-2797. DOI: 10.1021/Om5002843  0.648
2014 Hopmann KH, Bayer A. Enantioselective imine hydrogenation with iridium-catalysts: Reactions, mechanisms and stereocontrol Coordination Chemistry Reviews. 268: 59-82. DOI: 10.1016/J.Ccr.2014.01.023  0.71
2013 Melnes S, Bayer A, Gautun OR. Aryl N-methyliminodiacetic acid (MIDA) boronates from cyclotrimerization of ethynyl MIDA boronate with diynes Tetrahedron. 69: 7910-7915. DOI: 10.1016/J.Tet.2013.07.027  0.484
2013 Kostenko N, Ericsson C, Engqvist M, Gonzalez SV, Bayer A. Palladium(0)-catalyzed cross-couplings of 2-bromophosphinine European Journal of Organic Chemistry. 4756-4759. DOI: 10.1002/Ejoc.201300710  0.339
2012 Melnes S, Bayer A, Gautun OR. Cyclotrimerization of unsymmetrically bromo-substituted diynes: toward the synthesis of potential selective inhibitors of tyrosine kinase 2 Tetrahedron. 68: 8463-8471. DOI: 10.1016/J.Tet.2012.07.087  0.453
2011 Hopmann KH, Bayer A. On the Mechanism of Iridium-Catalyzed Asymmetric Hydrogenation of Imines and Alkenes: A Theoretical Study Organometallics. 30: 2483-2497. DOI: 10.1021/Om1009507  0.685
2006 Endeshaw MM, Bayer A, Hansen LK, Gautun OR. Catalytic Asymmetric Hetero Diels–Alder Reactions of N‐Sulfinyl Dienophiles with Chiral Bis(oxazoline)copper(II) and ‐zinc(II) Triflates European Journal of Organic Chemistry. 2006: 5249-5259. DOI: 10.1002/Ejoc.200600083  0.447
2004 Bayer A, Endeshaw MM, Gautun OR. Asymmetric hetero-Diels-Alder reactions of N-sulfinyl dienophiles using chiral bis(oxazoline)-copper(II) and -zinc(II) triflates. Journal of Organic Chemistry. 69: 7198-7205. PMID 15471469 DOI: 10.1021/Jo0490245  0.519
2002 Bayer A, Hansen LK, Gautun OR. Asymmetric Diels–Alder reactions of N-sulfinyl dienophiles using chiral Ti(IV) Lewis acids Tetrahedron-Asymmetry. 13: 2407-2415. DOI: 10.1016/S0957-4166(02)00661-4  0.456
2001 Bayer A, Gautun OR. Highly enantioselective hetero Diels–Alder reactions of N-sulfinyl dienophiles promoted by copper(II)- and zinc(II)-chiral bis(oxazoline) complexes Tetrahedron-Asymmetry. 12: 2937-2939. DOI: 10.1016/S0957-4166(01)00525-0  0.374
2001 Bayer A, Svendsen JS. Substrate Binding in the Asymmetric Dihydroxylation Reaction − Investigation of the Stereoselectivity in the Dihydroxylation ofCs-Symmetric Divinylcarbinol Derivatives European Journal of Organic Chemistry. 2001: 1769-1780. DOI: 10.1002/1099-0690(200105)2001:9<1769::Aid-Ejoc1769>3.0.Co;2-D  0.445
2000 Bayer A, Gautun OR. Asymmetric N-sulfinyl dienophile Diels–Alder cycloadditions using chiral Ti(IV)-based Lewis acids Tetrahedron Letters. 41: 3743-3746. DOI: 10.1016/S0040-4039(00)00480-9  0.385
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