Publications
2025
129. "Functional group tolerant iron-catalyzed cyclotrimerization of terminal and internal alkynes" Benedict Klinnert and Bernd Plietker, Communications Chemistry 2025, 8, 410. DOI
128. "Chiral two-dimensional conjugated metal-organic frameworks with high spin polarization" Shiyi Feng, Yang Lu, Chenchen Wang, Morteza Torabi, Xing Huang, Florian Auras, Ran He, Lukas Sporrer, Paul-Alexander Laval-Schmidt, Xizheng Wu, Xia Wang, Li Wan, Dongxu Wang, Bernd Plietker, Mike Hambsch, Markus Löffler, Stefan C. B. Mannsfeld, Claudia Felser and Xinliang Feng, Nature Communications 2025, 16, 9473. DOI
127. "Multiple oestradiol functions inhibit ferroptosis and acute kidney injury" Wulf Tonnus, Francesca Maremonti, Shubhangi Gavali, Marlena Nastassja Schlecht, Florian Gembardt, Alexia Belavgeni, Nadja Leinung, Karolin Flade, Natalie Bethe, Sofia Traikov, Anne Haag, Danny Schilling, Sider Penkov, Melodie Mallais, Christine Gaillet, Claudia Meyer, Melika Katebi, Anushka Ray, Louisa M. S. Gerhardt, Anne Brucker, Jorunn Naila Becker, Mirela Tmava, Lisa Schlicker, Almut Schulze, Nina Himmerkus, Andrej Shevchenko, Mirko Peitzsch, Uladzimir Barayeu, Sonia Nasi, Juliane Putz, Kenneth S. Korach, Joel Neugarten, Ladan Golestaneh, Christian Hugo, Jan Ulrich Becker, Joel M. Weinberg, Svenja Lorenz, Bettina Proneth, Marcus Conrad, Eckhard Wolf, Bernd Plietker, Raphaël Rodriguez, Derek A. Pratt, Tobias P. Dick, Maria Fedorova, Stefan R. Bornstein und Andreas Linkermann, Nature 2025, 645, 1011–1019. DOI
126. "Interfacial Passivation for Enhanced Moisture Stability of Perovskite Solar Cells: Ammonium or Sulfonium?" Oscar Telschow, Angelika Wrzesi´nska-Lashkova, Shivam Singh, Vladimir Shilovskikh, Fulya Koc, Jianan Li, L. Andrés Guerrero-León, Boris Rivkin, Bernd Plietker and Yana Vaynzof, Advanced Materials Interfaces 2025, 12, 2400956. DOI
2024
125. "Reagent- and Ligand-Dependent Mechanistic Trichotomy in Fe-Catalyzed Borylative Cyclizations of Enynes" Fabian Rami, Benedict Klinnert, Jan Nowak, Franziska Ullwer, Min Zheng, Wolfgang Frey, and Bernd Plietker, Organic Letters 2024 26 (30), 6370-6374. DOI
124. "Antimicrobial Evaluation of Two Polycyclic Polyprenylated Acylphloroglucinol Compounds: PPAP23 and PPAP53" Ammanath, Aparna Viswanathan, Miki Matsuo, Huanhuan Wang, Frank Kraus, Anton Bleisch, Philipp Peslalz, Majd Mohammad, Meghshree Deshmukh, Anne Grießhammer, Moushumi Purkayastha, Andreas Vorbach, Boris Macek, Heike Brötz-Oesterhelt, Lisa Maier, Dorothee Kretschmer, Andreas Peschel, Tao Jin, Bernd Plietker and Friedrich Götz, Int. J. Mol. Sci. 2024, 25, 8023. DOI
123. "Chemical Predictive Modelling and Natural Product-based Divergent Synthesis – Design of Type B PPAPs with Nanomolar Activities against MRSA" Philipp Peslalz, Andreas Vorbach, Anton Bleisch, ElisaLiberini, Frank Kraus, Flavia Izzo, Heike Brötz-Oesterhelt, Friedrich Götz, and Bernd Plietker Chem. Eur. J. 2024, e202401955, DOI
122: "Asymmetric Rh Diene Catalysis under Confinement: Isoxazole Ring-Contraction in Mesoporous Solids" Max Marshall, Zarifishan Dilruba, Ann-Katrin Beurer, Kira Bieck, Sebastian Emmerling, Felix Markus, Charlotte Vogler, Felix Ziegler, Marina Fuhrer, Sherri S. Y. Liu, Shravan R. Kousik, Wolfgang Frey, Yvonne Traa, Johanna R. Bruckner,Bernd Plietker, Michael R. Buchmeiser, Sabine Ludwigs,Stefan Naumann, Petia Atanasova, Bettina V. Lotsch, Anna Zens, and Sabine Laschat Eur. J. Org. Chem. 2024, e202400283 DOI
121. "Tosylazide as N1-Synthon: Iron-Catalyzed Nitrogenative Dimerization of Indoles to p‑Bisindolopyrazine Derivatives" Jianan Li, Xiaohan Sun, Evgenia Dmitrieva, Noel Israel, Fupeng Wu, Lin Yang, Renxiang Liu, Xinliang Feng, and Bernd Plietker Organic Letters 2024 26 (5), 1046-1050 DOI
120. "A Ru-catalyzed desulfonylative C-arylation of O-tosyl-hydroxamates", Guobao Li, Tilo Lücken, Bernd Plietker, Chem. Commun., 2024 DOI
2023
119. "Key to High Performance Ion Hybrid Capacitor: Weakly Solvated Zinc Cations" Peng Chen, Xiaohan Sun, Bernd Plietker, Michael Ruck, Adv. Sci. 2023, 2305532. DOI
118. "Selective Activation of a TRPC6 Ion Channel Over TRPC3 by Metalated Type-B Polycyclic Polyprenylated Acylphloroglucinols" Philipp Peslalz, Frank Kraus, Flavia Izzo, Anton Bleisch, Yamina El Hamdaoui, Ina Schulz, Andreas M. Kany, Anna K. H. Hirsch, Kristina Friedland, Bernd Plietker, J. Med. Chem. 2023, 66, 22, 15061–15072. DOI
117. "Unnatural Endotype B PPAPs as Novel Compounds with Activity against Mycobacterium tuberculosis" Philipp Peslalz, Mark Grieshober, Frank Kraus, Anton Bleisch, Flavia Izzo, Dajana Lichtenstein, Helen Hammer, Andreas Vorbach, Kyoko Momoi, Ulrich M. Zanger, Heike Brötz-Oesterhelt, Albert Braeuning, Bernd Plietker, Steffen Stenger, J. Med. Chem. 2023, 66, 22, 15073–15083, DOI
2022
116. ´Electrolyte for High-Energy- and Power-Density Zinc Batteries and Ion Capacitors´ Peng Chen, Xiaohan Sun, Tobias Pietsch, Bernd Plietker, Eike Brunner, Michael Ruck, Adv. Mater. 2022, 2207131, DOI
115. "Iron-Catalyzed Cycloisomerization and C−C Bond Activation to Access Non-canonical Tricyclic Cyclobutanes" Frederik Kramm, Franziska Ullwer, Benedict Klinnert, Min Zheng, Bernd Plietker, Angew. Chem. Int. Ed, 2022, e202205169, DOI
2021
114. "Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity" Sebastian T. Emmerling, Felix Ziegler, Felix R. Fischer, Dr. Roland Schloch, Prof. Matthias Bauer, Prof. Bernd Plietker, Prof. Michael R. Buchmeiser, Prof. Bettina V. Lotsch, Chem. Eur. J. 2021, 28, 8, DOI
113. "Ruthenium-Catalyzed Secondary Amine Formation Studied by Density Functional Theory" L. Hückmann, S. Álvarez-Barcia, M. Fuhrer, B. Plietker, J. Kästner, ChemCatChem 2021, 13, 1-7, DOI
2020
112. "Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer and Catalysis Approach" M. Benedikter, J. Musso, M. K. Kesharwani, K. L. Sterz, I. Elser, F. Ziegler, F. Fischer, B. Plietker, W. Frey, J. Kästner, M. Buchmeiser, J. van Slageren, M. Nowakowski, M. Bauer, M. R. Buchmeiser, ACS Catal. 2020, 10, 14810-14823, DOI
111. "Determining the Relative Configuration of Propargyl Cyclo-propanes by Co-Crystallization" F. Krupp, M.-I. Picher, W. Frey, B. Plietker, C. Richert, Synlett 2020, 31, A-D, DOI
110. "Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions", M. Kirchhof, K. Gugeler, F. R. Fischer, M. Nowakowski, A. Bauer, S. Alvarez-Barcia, K. Abitaev, M. Schnierle, Y. Qawasmi, W. Frey, A. Baro, D. P. Estes, . Sottmann, M. R. Ringenberg, B. Plietker, M. Bauer, J. Kästner, S. Laschat, Organometallics 2020, 39, 3131-3145, DOI
109. "Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity", F. Rami, F. Bächtle, B. Plietker, Catal. Sci. Technol. 2020, 10, 1492-1497, DOI
108. "Fe-Catalyzed Selective Cyclopropanation of Enynes under Photochemical or Thermal Conditions", M.-I. Picher, B. Plietker, Org. Lett. 2020, 22, 340-344, DOI
2019
107. "A Bu4N[Fe(CO)3(NO)]-catalyzed Hemetsberger-Knittel-indole synthesis", A. Baykal, B. Plietker, Eur. J. Org. Chem. 2019, 1145-1147, DOI
106. "Mild, selective Ru-catalyzed deuteration using D2O as deuterium source", P. Eisele, F. Ullwer, S. Scholz, B. Plietker, Chem. Eur. J. 2019, 25, 16550-16554, DOI
105. "Nucleophilic Iron Complexes in Proton-Transfer Catalysis: An Iron-Catalyzed Dimroth Cyclocondensation", A. Baykal, D. Zhang, J. Knelles, I. T. Alt, B. Plietker, Chem. Asian J. 2019, 14, 3003-3010, DOI
104. "Recent advances in Fe-catalyzed C-H aminations using azides as nitrene precursors", B. Plietker, A. Röske, Catal. Sci. Technol., 2019, 9, 4188-4197, DOI
103. "A Cyanide-Free Synthesis of Acylcyanides through Ru-Catalyzed C(sp3)-H-Oxidation of Benzylic Nitriles", P. Eisele, M. Bauder, S.-F. Hsu, B. Plietker, ChemistryOpen 2019, 8, 689-691, DOI
102. "Scope and limitations of TBA[Fe]-catalyzed carbene transfer to X-H-bonds - Indication for a mechanistic dichotomy", A. Röske, I. Alt, B. Plietker, ChemCatChem 2019, 11, 1-5, DOI
101. "beta-Ketoesters as Mono- or Bisnucleophiles: A Concise Enatioselective Total Synthesis of (-)-Englerin A and B", L. Guo, B. Plietker, Angew. Chem. Int. Ed. 2019, 58, 8346-8350, DOI; Angew. Chem. 2019, 131, 8434-8438, DOI
100. "The Polycyclic Polyprenylated Acylphloroglucinol Antibiotic PPAP 23 Targets the Membrane and Iron Metabolism in Staphylococcus aureus", H. Wang, F. Kraus, P. Popella, A. Baykal, C. Guttroff, P. Francois, P. Sass, B. Plietker, F. Götz, Front. Microbiol., 2019, 10, DOI
2018
99. "Annelated cyclobutanes via Fe-catalyzed cycloisomerization of enyne acetates", F. Kramm, J. Teske, F. Ullwer, W. Frey, B. Plietker, Angew. Chem. Int. Ed. 2018, 57, 13335-13338, DOI
98. "Catalytic Enantioselective Total Synthesis of the Picrotoxane Alkaloids (-)-Dendrobine, (-)-Mubironine B, and (-)-Dendroxine", L. Guo, W. Frey, B. Plietker, Org. Lett. 2018, 20, 4328-4331, DOI
97. "Fe-catalyzed cycloisomerization of Aryl Allenyl Ketones: Access to 3-Arylidene-indan-1-ones", J. Teske, B. Plietker, Org. Lett. 2018, 20, 2257-2260, DOI
2017
96. "Detection and Characterization of Hydride Ligands in Iron Complexes by High-Resolution Hard X-Ray Spectroscopy and Implications for Catalytic Processes" L. Burkhardt, M. Holzwarth, B. Plietker, M. Bauer, Inorg. Chem. 2017, 56, 13300-13310, DOI
95. "Polycyclic polyprenylated acylphloroglucinols - an emerging class of non-peptide-based MRSA- and VRE-active antibiotics" C. Guttroff, A. Baykal, H. Wang, P. Popella, F. Kraus, N. Biber, S. Krauss, F. Götz, B. Plietker, Angew. Chem. Int. Ed. 2017, 56, 15852-15856, DOI
94. "Fe-Catalyzed Cycloisomerizations" J. Teske, B. Plietker, Isr. J. Chem. 2017, 57, DOI
93."Fe-catalyzed Intramolecular Aminations of C(sp3)-H-bonds of alkylarylazides" I. T. Alt, C. Guttroff, B. Plietker, Angew. Chem. Int. Ed. 2017, 56, 10582-10586, DOI; Angew. Chem. 2017, 129, 10718-10722, DOI
2016
92. “A Redox-Neutral Fe-Catalyzed Cycloisomerization of Enyne Acetates” J. Teske, B. Plietker, ACS Catalysis 2016, 6, 7148 DOI
91. “Fe-catalyzed reductive NO-bond cleavage – a route to the diastereoselective 1, 4-aminohydroxylation of 1, 3-dienes” S. Scholz, B. Plietker, Organic Chemistry Frontiers 2016, 3, 1295 DOI
90. “Selectivity Trends in Olefin Epoxidations Catalyzed by (NNNN)Manganese(+II) Complexes using Trifluoroethanol as the Solvent” S. Lorenz, B. Plietker, ChemCatChem 2016, (published online) DOI
89. “Iron‐Catalyzed Michael Addition of Ketones to Polar Olefins” D.H. Zhang, J. Knelles, B. Plietker, Adv. Synth. Cat. 2016, 358, 2469 DOI
88. „Enzyme-Catalyzed Carbonyl Olefination by the E. coli Protein YfeX in the Absence of Phosphines” M. J. Weissenborn, S.A. Löw, N. Borlinghaus, M. Kuhn, S. Kummer, F. Rami, B. Plietker, B. Hauer, ChemCatChem 2016, 8, 1636 DOI
87. „The Evolution of Fe-catalyzed Nucleophilic Activation of Acceptor-substituted Vinyl- and Arylcyclopropanes” C.-H. Lin, B. Plietker, Isr. J. Chem. 2016, 56, 409 DOI
86. "Die Eisen-katalysierte intramolekulare C(sp2)-H-Aminierung" I. T. Alt, B. Plietker, Angew. Chem. 2016, 128, 1542 DOI; Angew. Chem. Int. Ed. 2016, 55, 1519 DOI
85. "Iron-Catalyzed C-Allylating Partial Dearomatization of Naphthols" B. Heid and B. Plietker, Synthesis 2016, 48(03), 340 DOI
2015
84. "Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] – the Fe-catalyzed Cloke-Wilson rearrangement of vinyl and arylcyclopropanes" C.-H. Lin, D. Pursley, J. Klein, J. Teske, J. Allen, F. Rami, A. Koehn and B. Plietker, Chem. Sci. 2015, 6, 7034 DOI
83. "General Stereodivergent Enantioselective Total Synthetic Approach toward Macrosphelides A–G and M" C. Häcker, B. Plietker, J. Org. Chem. 2015, 80, 8055 DOI
82. „Dual [Fe+Phosphine] Catalysis: Application in Catalytic Wittig Olefination“, S. Rommel, C. Belger, J.-M. Begouin, B. Plietker, ChemCatChem 2015, 7, 1292 DOI
81. „The Enantioselective Total Synthesis of (+)-Clusianone“, F. Horeischi, C. Guttroff, B. Plietker, Chem. Commun. 2015, 51, 2259 DOI
80. „Total Synthesis and Absolute Configuration Assignment of MRSA Active Garcinol and Isogarcinol“, C. Socolsky, B. Plietker, Chem. Eur. J. 2015, 21, 3053 DOI
2014
79. „Insertion of Imines into Vinylcyclopropanes Catalyzed by Nucleophilic Iron Complexes: A Formal [3+2]-Cycloaddition Strategy for the Synthesis of Substituted Pyrrolidine Derivatives“, D. Pursley, B. Plietker, Synlett 2014, 25, 2316 DOI
78. „Fe-Catalyzed Nucleophilic Activation of C–Si versus Allylic C–O Bonds: Catalytic Trifluoromethylation of Carbonyl Groups versus Tandem Trifluormethylation–Allylation of Olefins“, J. E. M. N. Klein, S. Rommel, B. Plietker, Organometallics 2014, 33, 5802 DOI
77. „Fe or Fe-NO Catalysis? A Quantum Chemical Investigation of the [Fe(CO)3(NO)]−-Catalyzed Cloke–Wilson Rearrangement“, J. E. M. N. Klein, G. Knizia, B. Miehlich, J. Kästner, B. Plietker, Chem. Eur. J. 2014, 20, 7254 DOI
76. „Cooperative Catalysis: Electron-rich Fe-H-complexes and DMAP, a successful "joint-venture" for the ultrafast hydrogen production“, S. Rommel, L. Hettmanczyk, J. E. M. N. Klein, B. Plietker, Chem. Asian J. 2014, 9, 2140 DOI
75. „Eine Ru-Katalyse-basierende wieder aufladbare H2-Batterie“, S.-F. Hsu, S. Rommel, P. Eversfield, K. Muller, E. Klemm, W. R. Thiel, B. Plietker, Angew. Chem. 2014, 126, 7194 DOI
74. „The total syntheses of guttiferone A and 6-epi-guttiferone A“, F. Horeischi, N. Biber, B. Plietker, J. Am. Chem. Soc. 2014, 136, 4026. DOI
73. „Selective transfer hydrogenation and hydrogenation of ketones using a defined monofunctional (P^N(Bn)^N(Bn)^P)Ru(+II)-complex“, S.-F. Hsu, B. Plietker, Chem. Eur. J. 2014, 20, 4242. DOI
72. „The Electronic Ground State of [Fe(CO)3(NO)]−: A Spectroscopic and Theoretical Study“, J. E. M. N. Klein, B. Miehlich, M. S. Holzwarth, M. Bauer, M. Milek, M. M. Khusniyarov, G. Knizia, H.-J. Werner, B. Plietker, Angew. Chem. Int. Ed. 2014, 53, 1790. DOI
71. „Spectroelectrochemical investigation of Bu4N[Fe(CO)3(NO)]: identification of a reversible EC-mechanism“, F. Weisser, J. E. M. N. Klein, B. Sarkar, B. Plietker, Dalton Trans. 2014, 43, 883. DOI
2013
70. „Mild Hydrosulfenylation of Olefins under Neutral Conditions Using a Defined NHC-Ligated Iron–Sulfur Catalyst“, I. Alt, P. Rohse, B. Plietker, ACS Catal. 2013, 3, 3002. DOI
69. „The bidirectional total synthesis of sampsonione P and hyperibone I“, K. Lindermayr, B. Plietker, Angew. Chem. 2013, 52, 12183. DOI
68. „Redoxactive triazolium-derived ligands in nucleophilic Fe-catalysis – reactivity profile and development of a regioselective O-allylation“, J. E. M. N. Klein, M. S. Holzwarth, S. Hohloch, B. Sarkar, B. Plietker, Eur. J. Org. Chem. 2013, 2013, 6310. DOI
67. „A Mild Chemoselective Ru-Catalyzed Reduction of Alkynes, Ketones, and Nitro Compounds“, T. Schabel, C. Belger, B. Plietker, Org. Lett. 2013, 15, 2858. DOI
66. „Carbonylation of Alkyl Halides with [Fe(CO)3(NO)]-: In Silico Identification of a Common Intermediate“, J. E. M. N. Klein, B. Miehlich, J. Kästner, B. Plietker, Dalton Trans. 2013, 42, 7519. DOI
65. „Microwave Accelerated Ru-catalyzed Hydrovinylation of Alkynes and Enynes – A straightforward approach toward 1,3-Dienes and 1,3,5-Trienes“, T. Schabel, B. Plietker, Chem. Eur. J. 2013, 19, 6938. DOI
64. „The Ru-catalyzed alkylative dearyloxylation of lignin-type 2-aryloxyethanols“, D. Weickmann, B. Plietker, ChemCatChem 2013, 5, 2170. DOI
63. „Iron-catalysed carbon-carbon single bond activation“, J. E. M. N. Klein, B. Plietker, Org. Biomol. Chem. 2013, 11, 1271. DOI
62. „The Fe-catalyzed phosphono allylation of activated olefins“, S. Rommel, A. P. Dieskau, B. Plietker, Eur. J. Org. Chem. 2013, 2013, 1790. DOI
61. „Synchronizing steric and electronic effects in (NNNN,P)Ru(II)-complexes - the catalytic dehydrative alkylation of anilines using alcohols as a case study“, D. Weickmann, W. Frey B. Plietker, Chem. Eur. J. 2013, 19, 2741. DOI
60. „Biorelevant Metals in Sustainable Metal Catalysis - A Survey“, M. S. Holzwarth, B. Plietker, ChemCatChem 2013, 5, 1650. DOI
59. „PNNP-ligated Ru(II)-complexes are efficient catalysts for the mild benzylic C-H oxidation“, S.-F. Hsu, B. Plietker, ChemCatChem 2013, 5, 126. DOI
58. „Selective Catalytic Oxidation of C-H bond with Molecular Oxygen“, S. Laschat, E. Roduner, W. Kaim, B. Sarkar, V. B. Urlacher, J. Pleiss, R. Gläser, W.-D. Einicke, G. A. Sprenger, U. Beifuß, E. Klemm, C. Liebner, H. Hieronymus, S.-F. Hsu, B. Plietker, ChemCatChem 2013, 5, 82. DOI
2012
57. „Iron-Catalyzed Allylic Substitutions“, M. Jegelka, B. Plietker, in "Asymmetric Synthesis II - More Methods and Applications" (Ed. M. Christmann, S. Bräse), Wiley-VCH, Weinheim, 2012.
56. „Aryl-Aryl Interactions as Directing Motifs in the Stereodivergent Iron-catalyzed Hydrosilylation of Diarylalkynes“, C. Belger, B. Plietker, Chem. Comm. 2012, 48, 5419. DOI
55. „Katalytische Aktivierung von Diazoverbindungen mit elektronenreichen, definierten Eisen-Komplexen für Carben-Transfer-Reaktionen“, M. S. Holzwarth, I. Alt, B. Plietker, Angew. Chem. 2012, 124, 5447. DOI
54. „Fe-catalyzed Allylic C-C-bond Activation – Vinylcyclopropanes as versatile a1,a3,d5-Synthons in Traceless Allylic Substitutions and [3+2]-Cycloadditions“, A. P. Dieskau, M. S. Holzwarth, B. Plietker, J. Am. Chem. Soc. 2012, 134, 5048. DOI
53. „Dual Catalysis: Vinyl Sulfones through Tandem Iron-catalyzed Allylic Sulfonation Amine-catalyzed Isomerization“, M. Jegelka, B. Plietker, ChemCatChem 2012, 4, 329. DOI
52. „Fe-catalyzed multi-component reactions: The regioselective alkoxy allylation of activated olefins and its application in sequential Fe-catalysis“, A. P. Dieskau, M. S. Holzwarth, B. Plietker, Chem. Eur. J. 2012, 18, 2423. DOI
51. „Allylic Substitutions Catalyzed by Miscellaneous Metals“, J.-M. Begouin, J. E. M. N. Klein, D. Weickmann, B. Plietker, Top. Organomet. Chem. 2012, 38, 269.
2011
50. „A Mild Ligand-free Iron-catalyzed Liberation of Alcohols from Allylcarbonates“, A. P. Dieskau, B. Plietker, Org. Lett. 2011, 13, 5544. DOI
49. „The Total Synthesis of Hyperpapuanone, Hyperibone L, epi-Clusianone and Oblongifolin A“, N. Biber, K. Möws, B. Plietker, Nature Chemistry 2011, 3, 938. DOI
48. „Binuclear Fe-Complexes as Catalyst for the Ligand-free Regioselective Allylic Sulfenylation“, M. S. Holzwarth, W. Frey, B. Plietker, Chem. Comm. 2011, 47, 11113. DOI
47. „α-Sulfonyl Succinimides: Versatile Sulfinate Donors in Fe-Catalyzed, Salt-Free, Neutral Allylic Substitution“, M. Jegelka, B. Plietker, Chem. Eur. J. 2011, 17, 10417. DOI
46. „Fe-Catalyzed Thioesterification of Carboxylic Esters“, S. Magens, B. Plietker, Chem. Eur. J. 2011, 17, 8807. DOI
45. „Bu4N[Fe(CO)3(NO)]-Catalyzed Hydrosilylation of Aldehydes and Ketones”, A. P. Dieskau, J.-M. Begouin, B. Plietker, Eur. J. Org. Chem. 2011, 5291. DOI
44. „Advances in Sustainable Metal Catalysis: Iron Catalysis (Topics in Organometallic Chemistry)“ (Ed.: B. Plietker), Springer-Verlag, Heidelberg, 2011.
43. „Catalysis by Means of Complex Ferrates“, M. Jegelka, B. Plietker, Top. Organomet. Chem. 2011, 33, 177.
2010
42. „A Selective Ru-Catalyzed Semireduction of Alkynes to Z Olefins under Transfer-Hydrogenation Conditions“, C. Belger, N. M. Neisius, B. Plietker, Chem. Eur. J. 2010, 16, 12214. DOI
41. „Sustainability in Catalysis - Concept or Contradiction“, B. Plietker, Synlett 2010, 14, 2049.
40. „Nucleophilic Iron Catalysis in Transesterifications - Scope and Limitations“ S. Magens, B. Plietker, J. Org. Chem. 2010, 75, 3715. DOI
2009
39. „7,7-Dimethyl-4a-(3-methylbut-2-enyl)-2-oxo-4a,5,6,7-tetrahydro-2H-chromen-4-yl benzoate“, K. Möws, M. Schürmann, H. Preut, B. Plietker, Acta Cryst. 2009, E65, o2139. DOI
38. „7,7-Dimethyl-3,3,4a-tris(3-methylbut-2-enyl)-4a,5,6,7-tetrahydro-2H-chromene-2,4(3H)-dione“, K. Möws, M. Schürmann, H. Preut, B. Plietker, Acta Cryst. 2009, E65, o1751. DOI
37. „Präformierte π-allyl-Eisen-Komplexe als potente, definierte Katalysatoren für die allylische Substitution“, M. Holzwarth, A. Dieskau, M. Tabassam, B. Plietker, Angew. Chem. 2009, 121, 7387; Angew. Chem. Int. Ed. 2009, 48, 7251. DOI
36. „Selective C−S Bond Formation via Fe-Catalyzed Allylic Substitution“, M. Jegelka, B. Plietker, Org. Lett. 2009, 11, 3462. DOI
35. „Die Ruthenium-katalysierte Hydrovinylierung interner Alkine – ein atomökonomischer Zugang zu hochsubstituierten 1,3-Dienen“, M. Neisius, B. Plietker, Angew. Chem. 2009, 121, 5863; Angew. Chem. Int. Ed. 2009, 48, 5752. DOI
34. „The reincarnation of the Hieber anion [Fe(CO)3(NO)]– - a new venue in nucleophilic metal catalysis“, B. Plietker, A. Dieskau, Eur. J. Org. Chem. 2009, 775. DOI
2008
33. „Iron-catalysis in Organic Synthesis” (Hrsg.: B. Plietker), Wiley-VCH, Weinheim, 2008.
32. „A General, Iterative and Modular Approach toward Carbohydrate Libraries Based on Ruthenium-Catalyzed Oxidative Cyclizations“, M. Niggemann, A. Jelonek, N. Biber, M. Wuchrer, B. Plietker, J. Org. Chem. 2008, 73, 7028. DOI
31. „A diastereoselective Ru-catalyzed cross-metathesis dihydroxylation sequence - an efficient approach toward enantiomerically enriched syn-diols", N. Matthias Neisius, B. Plietker, J. Org. Chem. 2008, 73, 3218. DOI
30. „New Approaches Towards Monoamino Polyglycerol Dendrons and Dendritic Triblock Amphiphiles", Monika Wyszogrodzka, Katrin Möws, Stefan Kamlage, Joanna Wodzinska, Bernd Plietker and Rainer Haag, Eur. J. Org. Chem. 2008, 53, 63. DOI
29. „A Nucleophilic Fe-Catalyst for Transesterfications under Neutral Conditions”, S. Magens, M. Ertelt, A. Jatsch, B. Plietker, Org. Lett. 2008, 10, 53. DOI
28. „Ligand dependant mechanistic dichotomy in iron-catalyzed allylic substitutions – σ-allyl- vs. π-allyl-mechanism”, B. Plietker, A. Dieskau, K. Möws, A. Jatsch, Angew. Chem. 2008, 120, 204; Angew. Chem. Int. Ed. 2008, 47, 198. DOI
2007
27. „Umfangreiches Gebiet in bekömmlichen Häppchen“ (Buchbesprechung: Asymmetric Synthesis – The Essentials“, Hrsg.: M. Christmann, S. Bräse, Wiley-VCH, Weinheim, 2007) B. Plietker, Nachrichten aus der Chemie, 2007.
2006
Patent: „Fe(-II)-Katalysatorsysteme“, zum Patent angemeldet (Deutschland: 102007009478.9)
26. „Die regioselektive Eisen-katalysierte allylische Aminierung“, B. Plietker, Angew. Chem. 2006, 118, 6200; Angew. Chem. Int. Ed. 2006, 45, 6053. DOI
25. „Product Class: Aliphatic and Alicyclic Aldehydes: Synthesis of Aldehydes by Hydrolysis”, B. Plietker, Science of Synthesis 2006, 25, 151.
24. „Eine hochregioselektive, salzfreie Eisen-katalysierte allylische Alkylierung“, B. Plietker, Angew. Chem. 2006, 118, 1497; Angew. Chem. Int. Ed. 2006, 45,1469. DOI
23. „Asymmetrische Synthese im Spiegel von Chemie und Biologie“, B. Plietker, Angew. Chem. 2006, 118, 196; Angew. Chem. Int. Ed. 2006, 45, 190. DOI
2005
Patent: „Eisen-katalysierte allylische Alkylierung“, zum Patent angemeldet (Deutschland: 102005040752.8; Europa: 06016610.5-2103; USA: 11/510,546; China: 200610171889.5; Japan: 2006-230984; Indien: 1508/CHE/2006). 2005
22. „Enantioselective Palladium-catalyzed Addition of 1,3-Dicarbonylcompounds to an Allene Derivative“, B. M. Trost, A. Simas, B. Plietker, C. Jäkel, J. Xie, Chem. Eur. J. 2005, 11, 7075. DOI
21. „New Oxidative Pathways for the Synthesis of α-Hydroxy ketones – the α-Hydroxylation and Ketohydroxylation”, B. Plietker, Tetrahedron: Asymmetry 2005, 16, 3453. DOI
20. „Selectivity vs. Reactivity – Recent Advances in RuO4-catalyzed Oxidations”, B. Plietker, Synthesis 2005, 2453. DOI
19. „The RuO4-catalyzed Ketohydroxylation – Part II. A Regio-, Chemo- and Stereoselectivity Study“, B. Plietker, Eur. J. Org. Chem. 2005, 1919. DOI
18. „RuCl3/CeCl3/NaIO4 – A new heterobimetallic oxidation system for the efficient dihydroxylation of unreactive olefins“, B. Plietker, M. Niggemann, J. Org. Chem. 2005, 70, 2402. DOI
2004
17. „The RuO4-catalyzed Ketohydroxylation – Part I. Development, Scope and Limitation”, B. Plietker, J. Org. Chem. 2004, 69, 8287. DOI
16. „The RuO4-catalysed Dihydroxylation, Ketohydroxylation and Mono Oxidation – Novel Oxidation Reactions for the Synthesis of Diols and α-Hydroxy Ketones”, B. Plietker, M. Niggemann, Org. Biomol. Chem. 2004, 2, 2403. DOI
15. „The Acid Accelerated Ruthenium-catalysed Dihydroxylation. Scope and Limitations”, B. Plietker, M. Niggemann, A. Pollrich, Org. Biomol. Chem. 2004, 2, 1116. DOI
14. „Chemiedozententagung 2004 in Dortmund“, B. Plietker, Nachrichten aus der Chemie, 2004, 599.
13. „Neuartige Oxidationskatalysatoren – Die Natur als Vorbild“, B. Plietker, UniReport 2004, 37, 21.
12. „Alkenes as Ketol Surrogates – The Asymmetric Synthesis of Acyloins”, B. Plietker, Org. Lett. 2004, 6, 289. DOI
2003
11. „Modern Organocopper Chemistry“, B. Plietker, Nachrichten aus der Chemie, 2003, 197.
10. „New Chiral Diamide Ligands Containing Redox-Active Hydroquinone Groups. Synthesis and Results in the Palladium(II)-Catalyzed 1,4-Diacetoxylation of 1,3-Dienes“, R. C. Verboom, B. J. Plietker, J.-E. Bäckvall, J. Organomet. Chem. 2003, 687, 508. DOI
9. „An Improved Protocol for the RuO4-catalyzed Dihydroxylation of Olefins“, B. Plietker, M. Niggemann, Org. Lett. 2003, 5, 3353. DOI
8. „The RuO4-catalyzed Ketohydroxylation of Olefins”, B. Plietker, J. Org. Chem. 2003, 68, 7123. DOI
7. „Palladium-catalyzed Asymmetric Addition of Pronucleophiles to Allenes”, B. M. Trost, C. Jäkel, B. Plietker, J. Am. Chem. Soc. 2003, 125, 4438. DOI
2002
6. „Kinetic Studies of Acetate Exchange in trans-4-Acetoxy-[η3-(1,2,3)-cyclohexenyl]palladium Complexes. Relevance for Asymmetric 1,4-Oxidation Reactions”, H. K. Cotton, R. C. Verboom, L. Johansson, B. J. Plietker, J.-E. Bäckvall, Organometallics 2002, 21, 3367. DOI
2001
5. „Synthesis of Highly Substituted Methylidene Cyclohexenes Using New Tandem Reactions with Sultones“, B. Plietker, D. Seng, R. Fröhlich, P. Metz, Eur. J. Org. Chem. 2001, 3669. DOI
2000
4. „High Pressure Intramolecular Diels-Alder Reactions of Vinylsulfonates and Vinylsulfonamides”, B. Plietker, D. Seng, R. Fröhlich, P. Metz, Tetrahedron 2000, 6, 873. DOI
1998
3. „New Tandem Reactions with Sultones”, P. Metz, B. Plietker, Tetrahedron Lett. 1998, 39, 7827. DOI
1997
2. „Recent Advances in the Synthetic Elaboration of Sultones”, P. Metz, U. Meiners, D. Seng, B. Plietker, Phosphorus, Sulfur, and Silicon 1997, 120, 345.
1996
1. „Desulfurization of Sultones with Simultaneous Methylenation”, P. Metz, D. Seng, B. Plietker, Tetrahedron Lett. 1996, 37, 3841. DOI
Patents
2024
5. Flavia Izzo; Frank Kraus; Philipp Peslalz; Anton Bleisch; Bernd Plietker: "4-Hydroxybicyclo[3.3.1]non-3-ene-2,9-dione derivatives, and use thereof" World Intellectual Property Organization, (2024), Language: English, WO2024099520A1
4. Philipp Peslalz; Christoph Heichert; Bernd Plietker: "Fluorescent 4-hydroxybicyclo[3.3.1]non-3-ene-2,9-dione derivatives, and their use " World Intellectual Property Organization, (2024), Language: English, WO2024099519A1
3. Frank Kraus; Flavia Izzo; Philipp Peslalz; Anton Bleisch; Bernd Plietker: "Salts and complexes with 3-acetal-4-hydroxybicyclo[3.3.1]non-3-ene-2.9.dione derivatives and use of these salts and complexes" World Intellectual Property Organization, (2024), Language: English, WO2024099518A1
2. Philipp Peslalz; Bernd Plietker: ”Fluorescent salts of 4-hydroxybicyclo[3.3.1]non-3-ene-2,9-dione derivatives, and use thereof” World Intellectual Property Organization, (2024), Language: English, WO2024099517A1
1. Anton Bleisch; Pascal Roßberg; Bernd Plietker: " Cyclized 3-acetal-4-hydroxybicyclo[3.3.1]non-3-ene-2.9.dione derivatives and their use" World Intellectual Property Organization, (2024), Language: English, WO2024099516A1