Publications of Alois Fürstner

Rummelt, S. M.; Radkowski, K.; Roşca, D.-A.; Fürstner, A. Interligand Interactions Dictate the Regioselectivity of Trans-Hydrometalations and Related Reactions Catalyzed by [Cp*RuCl]. Hydrogen Bonding to a Chloride Ligand as a Steering Principle in Catalysis. Journal of the American Chemical Society 2015, 137, 5506–5519.

Fuchs, M.; Fürstner, A. Trans-Hydrogenation: Application to a Concise and Scalable Synthesis of Brefeldin A. Angewandte Chemie International Edition 2015, 54, 3978–3982.

Hoffmeister, L.; Fukuda, T.; Pototschnig, G.; Fürstner, A. Total Synthesis of an Exceptional Brominated 4-Pyrone Derivative of Algal Origin: An Exercise in Gold Catalysis and Alkyne Metathesis. Chemistry – A European Journal 2015, 21, 4529–4533.

Valot, G.; Mailhol, D.; Regens, C. S.; O'Malley, D. P.; Godineau, E.; Takikawa, H.; Philipps, P.; Fürstner, A. Concise Total Syntheses of Amphidinolides C and F. Chemistry – A European Journal 2015, 21, 2398–2408.

Casitas, A.; Krause, H.; Goddard, R.; Fürstner, A. Elementary Steps of Iron Catalysis: Exploring the Links between Iron Alkyl and Iron Olefin Complexes for their Relevance in C—H Activation and C—C Bond Formation. Angewandte Chemie International Edition 2015, 54, 1521–1526.

Lehr, K.; Schulthoff, S.; Ueda, Y.; Mariz, R.; Leseurre, L.; Gabor, B.; Fürstner, A. A New Method for the Preparation of Non-Terminal Alkynes: Application to the Total Syntheses of Tulearin A and C. Chemistry – A European Journal 2015, 21, 219–227.

Mailhol, D.; Willwacher, J.; Kausch-Busies, N.; Rubitski, E. E.; Sobol, Z.; Schuler, M.; Lam, M.-H.; Musto, S.; Loganzo, F.; Maderna, A.; Fürstner, A. Synthesis, Molecular Editing, and Biological Assessment of the Potent Cytotoxin Leiodermatolide. Journal of the American Chemical Society 2014, 136, 15719–15729.

Fürstner, A. Quelques Commentaires sur la Catalyse : la Recherche Fondamentale Précède les Applications. Some Comments about Catalysis: Fundamental Research Precedes Applications. Comptes Rendus Chimie 2014, 17, 1065–1070.

Lhermet, R.; Fürstner, A. Cross-Metathesis of Terminal Alkynes. Chemistry - A European Journal 2014, 20, 13188–13193.

Seidel, G.; Fürstner, A. A Novel Boron Heterocycle Comprised of an Inner Boronium/Borate Adduct. Organometallics 2014, 33, 4336–4339.

Fürstner, A. Catalysis for Total Synthesis: A Personal Account. Angewandte Chemie International Edition 2014, 53, 8587–8598.

Wang, F.; Mielby, J.; Richter, F. H.; Wang, G.; Prieto, G.; Kasama, T.; Weidenthaler, C.; Bongard, H.-J.; Kegnæs, S.; Fürstner, A.; Schüth, F. A Polyphenylene Support for Pd Catalysts with Exceptional Catalytic Activity. Angewandte Chemie International Edition 2014, 53, 8645–8648.

Gebauer, K.; Fürstner, A. Total Synthesis of the Biphenyl Alkaloid (−)-Lythranidine. Angewandte Chemie International Edition 2014, 53, 6393–6396.

Guy, A.; Oger, C.; Heppekausen, J.; Signorini, C.; De Felice, C.; Fürstner, A.; Durand, T.; Galano, J.-M. Oxygenated Metabolites of n-3 Polyunsaturated Fatty Acids as Potential Oxidative Stress Biomarkers: Total Synthesis of 8-F_3t-IsoP, 10-F_4t-NeuroP and [D4]-10-F_4t-NeuroP. Chemistry - A European Journal 2014, 20, 6374–6380.

Seidel, G.; Fürstner, A. Structure of a Reactive Gold Carbenoid. Angewandte Chemie International Edition 2014, 53, 4807–4811.

Sun, C.-L.; Krause, H.; Fürstner, A. A Practical Procedure for Iron-Catalyzed Cross-Coupling Reactions of Sterically Hindered Aryl-Grignard Reagents with Primary Alkyl Halides. Advanced Synthesis & Catalysis 2014, 356, 1281–1291.

Willwacher, J.; Fürstner, A. Catalysis-Based Total Synthesis of Putative Mandelalide A. Angewandte Chemie International Edition 2014, 53, 4217–4221.

Hoffmeister, L.; Persich, P.; Fürstner, A. Formal Total Synthesis of Kendomycin by Way of Alkyne Metathesis/Gold Catalysis. Chemistry - A European Journal 2014, 20, 4396–4402.

Rummelt, S. M.; Fürstner, A. Ruthenium-Catalyzed Trans-Selective Hydrostannation of Alkynes. Angewandte Chemie International Edition 2014, 53, 3626–3630.

Fürstner, A. From Understanding to Prediction: Gold- and Platinum-Based π-Acid Catalysis for Target Oriented Synthesis. Accounts of Chemical Research 2014, 47, 925–938.