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Publications

Recent Examples of Claisen Rearrangements in Synthesis. Aichinger, C.; Rinner, U. in preparation.

Galbulimima Alkaloids. Rinner, U. In The Alkaloids: Chemistry and Biology; Knölker, H. J. Ed. 2017, Volume 78.

Tin Dioxide as a Photocatalyst for Water Treatment. Al-Hamdi, A. M.; Rinner, U.; Sillanpää, M.; Proc. Saf. Environ. Prot. 2017, 190.

Galanthamine. Rinner, U.; Dank, C.; Hudlicky, T. In Targets in Heterocyclic Systems; Attanasi, O. A.; Spinelli, D. Eds.; Italian Society of Chemistry, Rome, 2016, 286.

Tyrosine Alkaloids. Waser, M.; Rinner, U. In From Biosynthesis to Total Synthesis; Zografos, A., Ed.; John Wiley & Sons, Inc.: Hoboken; 2016, 431.

Monoterpenes and Iridoids. Rinner, U.; Waser, M.; In From Biosynthesis to Total Synthesis; Zografos, A., Ed.; John Wiley & Sons, Inc.: Hoboken; 2016, 196.

Progress in the Preparation of Jatrophane Diterpenes. Rinner, U. Eur. J. Org. Chem. 2015, 3197

Synthesis of the C6-C14 fragment of euphosalicin. Aichinger, C.; Mulzer, J.; Rinner, U. Synlett 201526, 1852.

Synthetic Studies Towards an Advanced Precursor of the Jatrophane Diterpene Pl-4. Fürst, R.; Lentsch, C.; Rinner, U. Synthesis, 201446, 357.

Jatrophane Diterpenes - Preparation of the Western Fragment of Pl-3. Lentsch, C.; Fürst, R.; Mulzer, J.; Rinner, U. Eur. J. Org. Chem2014, 919

Synthesis of Esters and Lactones. Siengalewicz, P.; Mulzer, J.; Rinner, U. In: Comprehensive Organic Synthesis II. Knochel, P. Ed. 2014, Elsevier, Amsterdam, p 355.

Enyne Metathesis Approach Towards the Cyclopentane Motif of Jatrophane Diterpenes. Lentsch, C.; Fürst, R.; Rinner, U. Synlett. 2013, 24, 2665.

Chiral Hydroxylation at the Mononuclear Nonheme Fe(II) Center of 4-(S)-Hydroxymandelate Synthase - A Structure-Activity-Relationship Analysis. Di Giuro, C. M. L.; Konstantinovics, C.; Nowikow, C.; Rinner, U.; Straganz, G. D. PLOS ONE, 2013, 8, 7, e68932.

Synthesis of an Advanced Intermediate of the Jatrophane Diterpene Pl-4 - a Dibromide Coupling Approach. Fürst, R.; Rinner, U. J. Org. Chem. 2013, 78, 8748.

Towards the Total Synthesis of Pl-3 - Preparation of the Eastern Fragment via a Diastereoselective SmI2-Mediated Reformatsky Reaction. Fürst, R.; Lentsch, C.; Rinner, U. Eur. J. Org. Chem. 2013, 2293.

Lycopodium Alkaloids - Synthetic Highlights and Recent Developments. Siengalewicz, P.; Mulzer J.; Rinner, U. In The Alkaloids: Chemistry and Biology; Knölker, H. J., Ed., 2013, Volume 72, 1.

Structure-Activity Relationships, Ligand Efficiency, and Lipophilic Profiles of Benzophenone-Type Inhibitors of Multidrug Transporter P-Glycoprotein. Jabeen, I,; Pleban, K.; Rinner, U.; Chiba, P.; Ecker, G. F. J. Med. Chem. 2012, 3261.

Synthesis of Morphine Alkaloids and Derivatives. Rinner, U.; Hudlicky, T. Top. Curr. Chem., 2012, 309, 33.

Chiral Pool Synthesis: Chiral Pool Syntheses from cis-Cyclohexadiene Diols Rinner, U. In: Carreira, E. M.; Yamamoto, H. Eds. Comprehensive Chirality, Volume 2, 2012, 240.

Selected Diastereoselective Reactions: Substrate controlled diastereoselective addition reactions of organocopper reagents. Siengalewicz, P.; Mulzer, J.; Rinner, U. In: Carreira, E. M.; Yamamoto, H. Eds. Comprehensive Chirality, Volume 2, 2012, 441.

Synthesis of Protoilludanes and related sesquiterpenes. Siengalewicz, P.; Mulzer, J.; Rinner, U. Eur. J. Org. Chem. 2011, 7041.

Chemoenzymatic Synthesis of Idesolide from Benzoic Acid. Adams, D. R. Aichinger, C.; Rinner, U.; Hudlicky, T. Synlett, 2011, 725.

Syntheses of Galbulimima Alkaloids. Rinner, U.; Lentsch, C.; Aichinger, C. Synthesis, 2010, 3763

Chemoenzymatic Synthesis of Amaryllidaceae Constituents and Biological Evaluation of their C-1 Analogues. The Next Generation Synthesis of 7-Deoxypancratistatin and trans-Dihydrolycoricidine. Collins, J.; Rinner, U.; Moser, M; Hudlicky, T.; Ghiviriga, I.; Romero, A.E.; Kornienko, A.; Ma, D.; Griffin, C.; Pandey, S. J. Org. Chem. 2010, 3069.

Synthesis and Antitumor-Evaluation of Cyclopropyl-Containing Combretastatin Analogs. Fürst, R.; Zupko, I.; Berenyi, A.; Ecker, G. F.; Rinner, U. Bioorg. Med. Chem. Lett. 2009, 6948.

General Synthesis of Highly Functionalized Cyclopentane Segments for the Preparation of Jatrophane Diterpenes. Lentsch, C.; Rinner, U. Org. Lett. 2009, 5326.

Elements of Synthesis Planning. By R. W. Hoffmann. Rinner, U.; Mulzer J. Angew. Chem., Int. Ed. 2009, 9590.

Recent Progress in the Total Synthesis of Naphthyridinomycin and Lemonomycin Tetrahydroisoquinoline Antitumor Antibiotics (TAAs). Siengalewicz, P.; Rinner, U.; Mulzer, J. Chem. Soc. Rev. 2008, 2676.

Total Synthesis of 7-Deoxypancratistatin-1-carboxaldehyde and Carboxylic Acid via Solvent-Free Intramolecular Aziridine Opening: Phenanthrene to Phenanthridone Cyclization Strategy. Collins, J.; Drouin, M.; Sun, Xuetong; Rinner, U.; Hudlicky, T. Org. Lett. 2008, 10, 361.

The Way of Synthesis. By Tomas Hudlicky and Joesphine W. Reed. Rinner, U; Mulzer, J. Angew. Chem., Int. Ed. 2008, 47, 31.

Cyclotrimerization approach to unnatural structural modifications of pancratistatin and other amaryllidaceae constituents - Synthesis and biological evaluation. Hudlicky, T.; Moser, M.; Banfield, S. C.; Rinner, U.; Chapuis, J. C.; Pettit, G. R. Can. J. Chem. 2006, 84, 1313.

Reactions of indole derivatives with oxiranes on silica. Synthesis of β-carbolin-1-one mimic of pancratistatin. Hudlicky T.; Rinner, U.; Finn, K., J.; Ghiviriga, I. J.  Org. Chem. 2005, 70, 3490. 

Synthesis of Amaryllidaceae Constituents – an Update. Rinner, U.; Hudlicky, T. Synlett 2005, 365.

b-Carboline-1-one mimic of the anticancer Amaryllidaceae constituent pancratistatin. Synthesis and biological evaluation. Rinner, U.; Hudlicky, T.; Gordon, H.; Pettit, G. R. Angew. Chem., Int. Ed. 2004, 43, 5342.

Unnatural Derivatives of Pancratistatin. Synthesis and Biological Activity. Rinner, U.; Hillebrenner, H. L.; Adams, D. R.; Hudlicky, T.; Pettit, G. R. Bioorg. Med. Chem. 2004, 14, 2911.

New application of Burgess reagent in its reaction with epoxides. Rinner, U.; Adams, D. R.; Santos, M. L.; Abboud, K. A.; Hudlicky, T.; Synlett, 2003, 1247.

Total synthesis and biological evaluation of Amaryllidaceae alkaloids: Narciclasine, ent-7-deoxypancratistatin, 10b-epi-deoxypancratistatin, and truncated derivatives. Hudlicky, T.; Rinner, U.; Gonzalez, D.; Akgun, H.; Schilling, S.; Martinot, T. A.; Pettit, G. R. J. Org. Chem. 2002, 67, 8726.

Selectivity of the (S)-oxynitrilase from Hevea brasiliensis towards a- and b-substituted aldehydes. Roda, G.; Riva, S.; Danieli, B.; Griengl, H.; Rinner, U.; Schmidt, M.; Mackova Zabelinskaja, A. Tetrahedron 2002, 58, 2979.

Total synthesis of epi-7-deoxypancratistatin via aza-Payne rearrangement and intramolecular cyclization. Rinner, U.; Siengalewicz, P.; Hudlicky, T. Org. Lett. 2002, 4, 115.

Structure assignment of aminoconduritols by 15N NMR correlation spectroscopy; synthesis of a positional isomer of 7-deoxypancratistatin. Schilling, S.; Rinner, U.; Chan, C.; Ghiviriga, I.; Hudlicky, T. Can. J. Chem. 2001, 1659.


Dr. Uwe Rinner
Institut für Organische Chemie
Universität Wien

Währinger Strasse 38
1090 Wien

T: +43-1-4277-52166
F: +43-1-4277-9251
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