Dirk Menche

Affiliations: 
2005-2008 Helmholtz Centre for Infection Research 
 2008-2011 Organisch-Chemisches Institut Ruprecht-Karls-Universität Heidelberg, Heidelberg, Baden-Württemberg, Germany 
 2011- Kekulé-Institut für Organische Chemie und Biochemie Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Nordrhein-Westfalen, Germany 
Website:
https://www.menche.uni-bonn.de/
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Publications

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Babczyk A, Menche D. (2023) Total Synthesis of Pentamycin by a Conformationally Biased Double Stille Ring Closure with a Trienyl-bis-stannane. Journal of the American Chemical Society. 145: 10974-10979
Gao X, Menche D. (2022) Sequential Methods for Di- and Tetrahydro-Pyranone Synthesis Enable Concise Access to Tuscolid δ-Lactone. Chemistry, An Asian Journal
Estévez-Gallego J, Álvarez-Bernad B, Pera B, et al. (2022) Chemical modulation of microtubule structure through the laulimalide/peloruside site. Structure (London, England : 1993)
Meringdal JW, Kilian A, Li WC, et al. (2022) Modular Synthesis of Halogenated Xanthones by a Divergent Coupling Strategy. The Journal of Organic Chemistry
Scheeff S, Rivière S, Ruiz J, et al. (2021) Modular Total Synthesis of -Archazolids and Archazologs. The Journal of Organic Chemistry
Scheeff S, Rivière S, Ruiz J, et al. (2021) Modular Total Synthesis of -Archazolids and Archazologs. The Journal of Organic Chemistry
Wollnitzke P, Essig S, Gölz JP, et al. (2020) Total Synthesis of Ajudazol A by a Modular Oxazole Diversification Strategy. Organic Letters. 22: 6344-6348
Wosniok PR, Knopf C, Dreisigacker S, et al. (2020) SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs. Chemistry (Weinheim An Der Bergstrasse, Germany)
Wingen L, Rausch M, Schneider T, et al. (2020) Modular Total Synthesis of Farnesyl Analogs of Cell Wall Precursors Lipid I and II, Containing the S. aureus Pentaglycine Bridge Modification. The Journal of Organic Chemistry
Wingen LM, Rausch M, Schneider T, et al. (2020) Synthesis of Tetramic Acid Fragments Derived from Vancoresmycin Showing Inhibitory Effects Towards S. aureus. Chemmedchem
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