Tindall, D. J.; Krause, H.; Fürstner, A. Iron-Catalyzed Cross-Coupling of 1-Alkynylcyclopropyl Tosylates and Related Substrates. Advanced Synthesis & Catalysis2016, 358, 2398–2403.
Casitas, A.; Krause, H.; Goddard, R.; Fürstner, A. Elementary Steps of Iron Catalysis: Exploring the Links between Iron Alkyl and Iron Olefin Complexes for their Relevance in C—H Activation and C—C Bond Formation. Angewandte Chemie International Edition2015, 54, 1521–1526.
Fürstner, A.; Martin, R.; Krause, H.; Seidel, G.; Goddard, R.; Lehmann, C. W. Preparation, Structure, and Reactivity of Nonstabilized Organoiron Compounds. Implications for Iron-Catalyzed Cross Coupling Reactions. Journal of the American Chemical Society2008, 130, 8773–8787.
Fürstner, A.; Majima, K.; Martín, R.; Krause, H.; Kattnig, E.; Goddard, R.; Lehmann, C. W. A Cheap Metal for a "Noble" Task: Preparative and Mechanistic Aspects of Cycloisomerization and Cycloaddition Reactions Catalyzed by Low-Valent Iron Complexes. Journal of the American Chemical Society2008, 130, 1992–2004.
Fürstner, A.; Alcarazo, M.; César, V.; Krause, H. Preparation of a Non-Symmetrical Imidazolium Salts: 1-Adamantyl-3-mesityl-4,5-dimethylimidazolium Tetrafluoroborate. Organic Syntheses2008, 85, 34–44.
Fürstner, A.; Alcarazo, M.; Krause, H.; Lehmann, C. W. Effective Modulation of the Donor Properties of N-Heterocyclic Carbene Ligands by "Through-Space" Communication within a Planar Chiral Scaffold. Journal of the American Chemical Society2007, 129, 12676–12677.
Fürstner, A.; Krause, H.; Lehmann, C. W. Unusual Structure and Reactivity of a Homoleptic "Super-Ate" Complex of Iron: Implications for Grignard Additions, Cross-Coupling Reactions, and the Kharasch Deconjugation. Angewandte Chemie International Edition2006, 45, 440–444.
Mamane, V.; Gress, T.; Krause, H.; Fürstner, A. Platinum- and Gold-Catalyzed Cycloisomerization Reactions of Hydroxylated Enynes. Journal of the American Chemical Society2004, 126, 8654–8655.
Scheiper, B.; Bonnekessel, M.; Krause, H.; Fürstner, A. Selective Iron-Catalyzed Cross-Coupling Reactions of Grignard Reagents with Enol Triflates, Acid Chlorides, and Dichloroarenes. The Journal of Organic Chemistry2004, 69, 3943–3949.
Fürstner, A.; Krause, H.; Thiel, O. R. Efficient relay syntheses and assessment of the DNA-cleaving properties of the pyrrole alkaloid derivatives permethyl storniamide A, lycogalic acid A dimethyl ester, and the halitulin core. Tetrahedron2002, 58, 6373–6380.
Fürstner, A.; Stelzer, F.; Rumbo, A.; Krause, H. Total synthesis of the turrianes and evaluation of their DNA- cleaving properties. Chemistry-A European Journal2002, 8, 1856–1871.
Fürstner, A.; Krause, H.; Lehmann, C. W. Preparation, structure and catalytic properties of a binuclear Pd(0) complex with bridging silylene ligands. Chemical Communications2001, 2001, 2372–2373.
Fürstner, A.; Krause, H. Practical Method for the Rhodium-Catalyzed Addition of Aryl- and Alkenylboronic Acids to Aldehydes. Advanced Synthesis & Catalysis2001, 343, 343–350.
Fürstner, A.; Krause, H. Flexible Synthesis of Metacycloprodigiosin and Functional Derivatives Thereofn. The Journal of Organic Chemistry1999, 64, 8281–8286.
Fürstner, A.; Alcarazo, M.; Krause, H. TETRAKIS(DIMETHYLAMINO)ALLENE; Ragan, J. A., Hrsg.; Ragan, J. A., Hrsg.; Organic Synthesis, Vol.86; John Wiley & Sons: Hoboken, NJ, 2009; Bd. 86, S 298–307.
TU Dortmund und Pantazis-Gruppe weisen in Kollaborationsprojekt eine neue Klasse von organischer Verbindung mit neutralem, einfach gebundenen Kohlenstoffatom nach
Dr. Dimitrios Pantazis, Gruppenleiter am MPI für Kohlenforschung in der Abteilung für molekulare Theorie und Spektroskopie, ist zum Vizepräsidenten der QBIC Society gewählt worden.
Mit Hilfe von Multiskalen-Simulationsmethoden und modernsten quantenchemischen Berechnungen untersuchten Dr. Dimitrios Pantazis und seine Gruppe, wie die Energie des Sonnenlichts in den Elektronenfluss umgewandelt wird, der chemische Reaktionen antreibt.