Publikationsliste Dr. Philipp Heretsch

Kleoff, M., Schwan, J., Christmann, M., & Heretsch, P. (2021). A Modular, Argon-Driven Flow Platform for Natural Product Synthesis and Late-Stage Transformations. Organic letters, 23(6), 2370-2374. doi.org/10.1021/acs.orglett.1c00661

Kleoff, M., Boeser, L., Baranyi, L., & Heretsch, P. (2021). Scalable Synthesis of Benzotriazoles via [3+2] Cycloaddition of Azides and Arynes in Flow. European Journal of Organic Chemistry, 2021(6), 979-982. doi.org/10.1002/ejoc.202001543

Reuss, F., & Heretsch, P. (2020). Synthetic strategies for the ibophyllidine alkaloids. Natural product reports, 38(4), 693-701. doi.org/10.1039/d0np00036a

Duecker, F. L., Heinze, R. C., Steinhauer, S., & Heretsch, P. (2020). Discoveries and Challenges en Route to Swinhoeisterol A. Chemistry - A European Journal, 26(44), 9971-9981. doi.org/10.1002/chem.202001405

Reuss, F., & Heretsch, P. (2020). Taxane Meets Propellane: First Chemical Synthesis of Highly Complex Diterpene Canataxpropellane. Angewandte Chemie - International Edition, 59(26), 10232-10234. doi.org/10.1002/anie.202002118

Reuss, F., & Heretsch, P. (2020). Synthesis of Aspidodispermine via Pericyclic Framework Reconstruction. Organic letters, 22(10), 3956-3959. doi.org/10.1021/acs.orglett.0c01242

Duecker, F. L., Heinze, R. C., Mueller, M., Zhang, S., & Heretsch, P. (2020). Synthesis of the Alleged Structures of Fortisterol and Herbarulide and Structural Revision of Herbarulide. Organic letters, 22(4), 1585-1588. doi.org/10.1021/acs.orglett.0c00180

Kleoff, M., Schwan, J., Boeser, L., Hartmayer, B., Christmann, M., Sarkar, B., & Heretsch, P. (2020). Scalable Synthesis of Functionalized Ferrocenyl Azides and Amines Enabled by Flow Chemistry. Organic letters, 22(3), 902-907. doi.org/10.1021/acs.orglett.9b04450

Schwan, J., Kleoff, M., Heretsch, P., & Christmann, M. (2020). Five-Step Synthesis of Yaequinolones J1 and J2. Organic letters, 22(2), 675-678. doi.org/10.1021/acs.orglett.9b04455

Duecker, F. L., Heinze, R. C., & Heretsch, P. (2020). Synthesis of Swinhoeisterol A, Dankasterone A and B, and Periconiastone A by Radical Framework Reconstruction. Journal of the American Chemical Society, 142(1), 104-108. doi.org/10.1021/jacs.9b12899