Mulzer et al. 2012
- Total Synthesis of Branimycin: An Evolutionary Approach
- A Non-Photochemical Approach to the Bicyclo[3.2.0]heptane Core of Bielschowskysin
- From Planning to Optimization: Total Synthesis of Valerenic Acid and Some Bioactive Derivatives
- Application of the Rodriguez-Pattenden Photo-Ring Contraction: Total Synthesis and Configurational Reassignment of 11-Gorgiacerol and 11-Epigorgiacerol
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Book Chapters
Comprehensive Chirality, Volume 2: Synthetic Methods I-Chiral Pool and Diastereoselective Methods
- General Principles of Diastereoselective Reactions: Rigid Templates
- General Principles of Diastereoselective Reactions:Diastereoselectivity via Substrate-Directable Reactions (Internal Delivery) and Heterocyclizations
- Chiral Pool Synthesis: from α-Amino Acids and Derivatives
- Chiral Pool Synthesis: Starting from Terpenes
- Selected Diastereoselective Reactions: Substrate Controlled Stereoselective Conjugate Addition Reactions with Organocopper Reagents
- Selected Diastereoselective Reactions:Diastereoselective Intra- and Intermolecular 1,3-Dipolr Cacloadditions in Natural Product Synthesis
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Strategies and Targets in Organic Synthesis
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Asymmetric Synthesis II: More Methods and Applications
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