Alexander Ripp

Projekt

Synthesis and Integration of Light-Responsive Molecules in Polymers
Zu Beginn meines Projekts synthetisiere und charakterisiere ich auf Licht reagierende Nukleoside. Später werde ich diese Nukleoside in Polymere, wie zum Beispiel DNA, einbauen. Das resultierende Material wird in der Lage sein, seine Eigenschaften als Reaktion auf Lichtstimulationen verschiedener Wellenlängen zu verändern.

Erstbetreuer

Prof. Dr. Henning Jessen

Publikationen in livMatS

• The aryne phosphate reaction*
  Haas, T., Wiesler, S., Dürr-Mayer, T., Ripp, A., Fouka, P., Qiu, D., & Jessen, H. (2021). The Aryne Phosphate Reaction. Angewandte Chemie. doi: 10.1002/ange.202113231
• Lost in Condensation: Poly-, Cyclo-, and Ultraphosphates*
  Jessen, H. J., Dürr-Mayer, T., Haas, T. M., Ripp, A., & Cummins, C. C. (2021). Lost in Condensation: Poly-, Cyclo-, and Ultraphosphates. Accounts of Chemical Research. doi: 10.1021/acs.accounts.1c00370
• The Aryne Phosphate Reaction*
  Haas, T., Wiesler, S., Dürr-Mayer, T., Ripp, A., Fouka, P., Qiu, D., & Jessen, H. (2021). The Aryne Phosphate Reaction. ChemRxiv. doi: 10.33774/chemrxiv-2021-3mfj8
• Thiocoumarin Caged Nucleotides: Synthetic Access and Their Photophysical Properties*
  Ma, J., Ripp, A., Wassy, D., Dürr, T.,Qiu, D., Häner, M., Haas, T., Popp, C., Bezold, D., Richert, S., Esser, B., Jessen, H. J. (2020). Thiocoumarin Caged Nucleotides: Synthetic Access and Their Photophysical Properties. Molecules, 25(22), 5325. doi: 10.3390/molecules25225325
• Rapid Synthesis of Nucleoside Triphosphates and Analogues*
  Ripp, A., Singh, J., & Jessen, H. (2020). Rapid Synthesis of Nucleoside Triphosphates and Analogues. Current Protocols in Nucleic Acid Chemistry, 81(1), e108. doi: 10.1002/cpnc.108
• Synthesis of Modified Nucleoside Oligophosphates Simplified: Fast, Pure, and Protecting Group Free*
  Singh, J., Ripp, A., Haas, T. M., Qiu, D., Keller, M., Wender, P. A., Siegel, J. S., Baldridge, K. K., & Jessen, H. J. (2019). Synthesis of modified nucleoside oligophosphates simplified: Fast, pure, and protecting group free. Journal of the American Chemical Society, 141(38), 15013-15017. doi: 10.1021/jacs.9b08273
  
  
  * Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy – EXC-2193/1 – 390951807