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


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


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


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


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


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


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


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


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


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. 


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.


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


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


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


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.


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


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


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


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


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


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


4. „High Pressure Intramolecular Diels-Alder Reactions of Vinylsulfonates and Vinylsulfonamides”, B. Plietker, D. Seng, R. Fröhlich, P. Metz, Tetrahedron 2000, 6, 873. DOI


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