Publikationen von Alois Fürstner

Yiannakas, E.; Grimes, M. I.; Whitelegge, J. T.; Fürstner, A.; Hulme, A. N. An Alkyne Metathesis Based Approach to the Synthesis of the Anti-malarial Macrodiolide Samroiyotmycin A. Angewandte Chemie International Edition 2021, 60, 18504–18508.

Haack, A.; Hillenbrand, J.; van Gastel, M.; Fürstner, A.; Neese, F. Spectroscopic and Theoretical Study on Siloxy-Based Molybdenum and Tungsten Alkylidyne Catalysts for Alkyne Metathesis. ACS Catalysis 2021, 11, 9086–9101.

Löffler, L. E.; Buchsteiner, M.; Collins, L. R.; Caló, F. P.; Singha, S.; Fürstner, A. [Rh₂(MEPY)₄] and [BiRh(MEPY)₄]: Convenient Syntheses and Computational Analysis of Strikingly Dissimilar Siblings. Helvetica Chimica Acta 2021, 104, e2100042.

Zachmann, R. J.; Fürstner, A. Light‐Driven gem‐Hydrogenation: An Orthogonal Entry into “Second Generation” Ruthenium Carbene Catalysts for Olefin Metathesis. Chemistry – A European Journal 2021, 27, 7663–7666.

Haack, A.; Hillenbrand, J.; Leutzsch, M.; van Gastel, M.; Neese, F.; Fürstner, A. Productive Alkyne Metathesis with “Canopy Catalysts” Mandates Pseudorotation. Journal of the American Chemical Society 2021, 143, 5643–5648.

Singha, S.; Buchsteiner, M.; Bistoni, G.; Goddard, R.; Fürstner, A. A New Ligand Design Based on London Dispersion Empowers Chiral Bismuth–Rhodium Paddlewheel Catalysts. Journal of the American Chemical Society 2021, 143, 5666–5673.

Herlé, B.; Späth, G.; Schreyer, L.; Fürstner, A. Total Synthesis of Mycinolide IV and Path‐Scouting for Aldgamycin N. Angewandte Chemie International Edition 2021, 60, 7893–7899.

Späth, G.; Fürstner, A. Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N. Angewandte Chemie International Edition 2021, 60, 7900–7905.

Löffler, L. E.; Wirtz, C.; Fürstner, A. Collective Total Synthesis of Casbane Diterpenes: One Strategy, Multiple Targets. Angewandte Chemie International Edition 2021, 60, 5316–5322.

Hess, S. N.; Mo, X.; Wirtz, C.; Fürstner, A. Total Synthesis of Limaol. Journal of the American Chemical Society 2021, 143, 2464–2469.

Fürstner, A. Lessons from Natural Product Total Synthesis: Macrocyclization and Postcyclization Strategies. Accounts of Chemical Research 2021, 54, 861–874.

Fürstner, A. Iron Catalyzed C-C-Bond Formation: From Canonical Cross Coupling to a Quest for New Reactivity. Bulletin of the Chemical Society of Japan 2021, 94, 666–677.

Schulthoff, S.; Hamilton, J. Y.; Heinrich, M.; Kwon, Y.; Wirtz, C.; Fürstner, A. The Formosalides: Structure Determination by Total Synthesis. Angewandte Chemie International Edition 2021, 60, 446–454.

Hillenbrand, J.; Leutzsch, M.; Gordon, C. P.; Copéret, C.; Fürstner, A. ¹⁸³W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis. Angewandte Chemie International Edition 2020, 59, 21758–21768.

Barsu, N.; Leutzsch, M.; Fürstner, A. Ruthenium-Catalyzed trans-Hydroalkynylation and trans-Chloroalkynylation of Internal Alkynes. Journal of the American Chemical Society 2020, 142, 18746–18752.

Peil, S.; Bistoni, G.; Goddard, R.; Fürstner, A. Hydrogenative Metathesis of Enynes via Piano-Stool Ruthenium Carbene Complexes Formed by Alkyne gem-Hydrogenation. Journal of the American Chemical Society 2020, 142, 18541–18553.

Biberger, T.; Zachmann, R. J.; Fürstner, A. Grubbs Metathesis Enabled by a Light‐Driven gem‐Hydrogenation of Internal Alkynes. Angewandte Chemie International Edition 2020, 59, 18423–18429.

Hillenbrand, J.; van Gastel, M.; Bill, E.; Neese, F.; Fürstner, A. Isolation of a Homoleptic Non-Oxo Mo(V) Alkoxide Complex: Synthesis, Structure and Electronic Properties of Penta-tert-Butoxymolybdenum. Journal of the American Chemical Society 2020, 142, 16392–16402.

Caló, F. P.; Fürstner, A. A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α‐Stannyl α‐Diazoacetate. "Stereoretentive" Stille Coupling with Formation of Chiral Quarternary Carbon Centers. Angewandte Chemie International Edition 2020, 59, 13900–13907.

Jin, H.; Fürstner, A. Modular Synthesis of Furans with up to Four Different Substituents by a trans‐Carboboration Strategy. Angewandte Chemie International Edition 2020, 59, 13618–13622.