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Department of Chemistry Johannes Gutenberg-University Mainz Duesbergweg 10-14, 55128 Mainz Room 2.223/02-125 Phone (06131) 39-25356 E-mail ferenc[at]uni-mainz.de |
Research interests: | synthetic organic chemistry |
Publications: | Six-Step Gram Scale Synthesis of the HIV Integrase Inhibitor Dolutegravir Sodium J.-P. Dietz, T. Lucas, J. Groß, S. Seitel, J. Brauer, D. Ferenc, B. F. Gupton, T. Opatz, Org. Process Res. Dev. 2021, 25, 1898–1910. Synthesis of 5-Fluorocytosine using 2-Cyano-2-fluoroethenolate as a Key Intermediate Total Synthesis of (−)-Oxycodone via Anodic Aryl–Aryl Coupling A Regio- and Diastereoselective Anodic Aryl-Aryl-Coupling in the Biomimetic Total Synthesis of (–)-Thebaine A Modular Access to (+/-)-Tubocurine and (+/-)-Curine - Formal Total Synthesis of Tubocurarine C. Schlemmer, C. Wiebe, D. Ferenc, D. Kowalczyk, S. Wedepohl, P. Ziegelmüller, J. Dernedde, T. Opatz, Chem. Asian J. 2014, 9, 2119-2125.Simple Two-Step Synthesis of 2,4-Disubstituted Pyrroles and 3,5-Disubstituted Pyrrole-2-carbonitriles from Enones M. Kücükdisli, D. Ferenc, M. Heinz, C. Wiebe, T. Opatz, Beilstein J. Org. Chem. 2014, 10, 466-470.Z-Amino(2-methyl-3-oxoisoindolin-1-ylidene)acetonitrile D. Schollmeyer, D. Ferenc, T. Opatz, Acta Cryst. 2009, E65, o3024.Synthesis of the CDK-Inhibitor Paullone by Cyclization of a Deprotonated α-Aminonitrile T. Opatz, D. Ferenc, Synthesis 2008, 3941-3944. Preparation of indoles from α-aminonitriles: a short synthesis of FGIN-1-27 Ring contracting rearrangements of 3-amino-4-(arylamino)-1H-isochromen-1-ones Facile preparation of 3-amino-4-(arylamino)-1H-isochromen-1-ones by a An unexpected three-component condensation leading to amino-(3-oxo-2,3-dihydro-1H-isoindol-1-ylidene)-acetonitriles |