Tost, Markus

Dr. Markus Tost

Gebäude C4 2, Büro E.03
Tel.: +49 681 302-6526
E-Mail

 

Arbeitsgebiet

Naturstoffsynthese via Matteson-Homologisierung

Publikationen

5   M. Tost, U. Kazmaier, “Synthesis of Oxylipids via a Boronic Ester Cycloetherification Approach", Org. Chem. Front. 2025, 12, 3288–3292. DOI: 10.1039/d5qo00213c

4   M. Tost, U. Kazmaier, “Stereoselective Syntheses of Highly Substituted Tetrahydrofurans based on Matteson Homologations", Chem Eur. J. 2025, 31, 202500560. DOI: 10.1002/chem.202500560

3   M. Tost, U. Kazmaier, "Synthesis and Late-Stage Modification of (–)‑Doliculide Derivatives Using Matteson's Homologation Approach", Mar. Drugs 2024, 22, 165. DOI: 10.3390/md22040165

2   M. Tost, U. Kazmaier, "Stereoselective Synthesis of Secondary and Tertiary Boronic Esters via Matteson Homologation", Org. Lett. 2023, 25, 6835–6839. DOI: 10.1021/acs.orglett.3c02360

1   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