Mulzer et al. 2009
- Total Syntheses of (+)-Echinopine A and B: Determination of Absolute Stereochemistry
- Synthesis and biological evaluation of a des-dihydropyran laulimalide analog
- Total Synthesis of the Antibiotic Kendomycin by Macrocyclization using Photo-Fries Rearrangement and Ring-Closing Metathesis
- Remarkable temperature effect on intramolecular [3 + 2] cyclization
- Decarboxylative Grob-Type Fragmentations in the Synthesis of Trisubstituted Z Olefins: Application to Peloruside A, Discodermolide, and Epothilone D
- Synthetic efforts towards the synthesis of the complex diterpene providencin
- A Desymmetrization Approach toward Highly Oxygenated cis-Decalins
- The Laulimalide Family: Total Synthesis and Biological Evaluation of Neolaulimalide, Isolaulimalide, Laulimalide and a Nonnatural Analogue
- A tetracarbonyl Paal-Knorr approach to semicorrins
- A Nine-Step Total Synthesis of (-)-Platencin
- Total Synthesis of Valerenic Acid, a Potent GABAA Receptor Modulator
- Total Synthesis of (-)-Penifulvin A, an Insecticide with a Dioxafenestrane Skeleton
- Total synthesis of epothilones A-F
Johann Mulzer
Institute for Organic Chemistry
University of Vienna
Währingerstraße 38
A-1090 Vienna
Institute for Organic Chemistry
University of Vienna
Währingerstraße 38
A-1090 Vienna