Synthesis of polyketide peptide conjugates

  • L. Karmann, K. Schulz, J. Herrmann, R. Müller, U. Kazmaier, "Total Syntheses and Biological Evaluation of Miuraenamides", Angew. Chem. 2015, 127, 4585–4590; Angew. Chem. Int. Ed. 2015, 54, 4502–4507.
  • D. Becker, U. Kazmaier, "Synthesis of Simplified Halogenated Chondramide Derivatives as new Actin-binding Agents", Eur. J. Org. Chem. 2015, 2591–2602.
  • D. Becker, U. Kazmaier, "Synthesis and Biological Evaluation of Dichlorinated Chondramide Derivatives", Eur. J. Org. Chem. 2015, 4198–4213.
  • F. A. Gegenfurtner, T. Zisis, N. Al Danaf, W. Schrimpf, Z. Kliesmete, C. Ziegenhain, W. Enard, U. Kazmaier, D. C. Lamb, A. M. Vollmar, S. Zahler, "Transcriptional effects of actin binding compounds: the cytoplasm sets the tone", Cell. Mol. Life Sci. 2018, 75, 4539–4555.
  • S. Kappler, L. Karmann, C. Prudel, J. Herrmann, G. Caddeu, R. Müller, A. M. Vollmar, S. Zahler, U. Kazmaier, "Synthesis and biological evaluation of (modified) miuraenamides", Eur. J.Org. Chem. 2018, 6952–6965.
  • J. Gorges, U. Kazmaier, "Matteson Homologation-based Total Synthesis of Lagunamide A", Org. Lett. 2018, 20, 2033−2036.
  • P. Servatius, T. Stach, U. Kazmaier, "Total synthesis of luminmycin A, a cryptic natural product from Photorhabdus luminescens", Eur. J. Org. Chem. 2019, 3163–3168.
  • S. Wang, A. Crevenna, I. Ugur, A. Marion, I. Antes, U. Kazmaier, M. Hoyer, D. Lamb, F. Gegenfurtner, Z. Kliesmete, C. Ziegenhain, W. Enard, A. Vollmar, S. Zahler, "Actin stabilizing compounds show specific biological effects due to their binding mode", Sci. Rep. 2019, 9, 9731.
  • S. Kappler, U. Kazmaier, “Synthesis of modified miuraenamides – the Ugi approach”, Arkivoc 2021, IV, 280–296. DOI: 10.2174/1570179418666210113161550.
  • O. Andler, U. Kazmaier, “A straightforward synthesis of polyketides via ester dienolate Matteson homologation”, Chem. Eur. J.  2021, 27, 949–953. DOI: 10.1002/chem.202004650.
  • O. Andler, U. Kazmaier, “Total Synthesis of Apratoxin A and B using Matteson´s Homologation Approach”, Org. Biomol. Chem.  2021, 19, 4866–4870. DOI: 10.1039/d1ob00713k.
  • M. Tost, O. Andler, U. Kazmaier, “A Matteson homologation-based synthesis of doliculide and derivatives”, Eur. J. Org. Chem. 2021, 6459–6471. DOI: 10.1002/ejoc.202101345.
  • O. Andler, U. Kazmaier, “Stereoselective Synthesis of a Protected Side Chain of Meliponamycin A”, Org. Lett. 2022, 24, 2541−2545. DOI: 10.1021/acs.orglett.2c00701.