Publikationen von Alois Fürstner

Huwyler, N.; Radkowski, K.; Rummelt, S. M.; Fürstner, A. Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes. Chemistry – A European Journal 2017, 23, 12412–12419.

Wang, Y.; Lee, S.; Lam, W.; Chen, S.-R.; Dutschman, G. E.; Gullen, E. A.; Grill, S. P.; Cheng, Y.; Fürstner, A.; Francis, S.; Baker, D. C.; Yang, X.; Lee, K.-H.; Cheng, Y.-C. Tylophorine Analogs Allosterically Regulates Heat Shock Cognate Protein 70 And Inhibits Hepatitis C Virus Replication. Scientific Reports 2017, 7, 10037.

Casitas, A.; Rees, J. A.; Goddard, R.; Bill, E.; DeBeer, S.; Fürstner, A. Two Exceptional Homoleptic Iron(IV) Tetraalkyl Complexes. Angewandte Chemie International Edition 2017, 56, 10108–10113.

Preindl, J.; Schulthoff, S.; Wirtz, C.; Lingnau, J.; Fürstner, A. Polyunsaturated C-Glycosidic 4-Hydroxy-2-pyrone Derivatives: Total Synthesis Shows that Putative Orevactaene Is Likely Identical with Epipyrone A. Angewandte Chemie International Edition 2017, 56, 7525–7530.

Sommer, H.; Hamilton, J. Y.; Fürstner, A. A Method for the Late-Stage Formation of Ketones, Acyloins, and Aldols from Alkenylstannanes: Application to the Total Synthesis of Paecilonic Acid A. Angewandte Chemie International Edition 2017, 56, 6161–6165.

Debrouwer, W.; Fürstner, A. Rearrangement of a Transient Gold Vinylidene into Gold Carbenes. Chemistry – A European Journal 2017, 23, 4271–4275.

Rummelt, S. M.; Cheng, G.-J.; Gupta, P.; Thiel, W.; Fürstner, A. Hydroxy-Directed Ruthenium-Catalyzed Alkene/Alkyne Coupling: Increased Scope, Stereochemical Implications, and Mechanistic Rationale. Angewandte Chemie International Edition 2017, 56, 3599–3604.

Roşca, D.-A.; Radkowski, K.; Wolf, L. M.; Wagh, M.; Goddard, R.; Thiel, W.; Fürstner, A. Ruthenium-Catalyzed Alkyne trans-Hydrometalation: Mechanistic Insights and Preparative Implications. Journal of the American Chemical Society 2017, 139, 2443–2455.

Sommer, H.; Fürstner, A. Stereospecific Synthesis of Fluoroalkenes by Silver-Mediated Fluorination of Functionalized Alkenylstannanes. Chemistry – A European Journal 2017, 23, 558–562.

Schaubach, S.; Michigami, K.; Fürstner, A. Hydroxyl-Assisted trans-Reduction of 1,3-Enynes: Application to the Formal Synthesis of (+)-Aspicilin. Synthesis 2017, 48, 202–208.

Fürstner, A. Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion. ACS Central Science 2016, 2, 778–789.

Cromm, P. M.; Wallraven, K.; Glas, A.; Bier, D.; Fürstner, A.; Ottmann, C.; Grossmann, T. N. Constraining an Irregular Peptide Secondary Structure through Ring-Closing Alkyne Metathesis. ChemBioChem: A European Journal of Chemical Biology 2016, 17, 1915–1919.

Echeverria, P.-G.; Fürstner, A. An Iron-Catalyzed Bond-Making/Bond-Breaking Cascade Merges Cycloisomerization and Cross-Coupling Chemistry. Angewandte Chemie International Edition 2016, 55, 11188–11192.

Werlé, C.; Goddard, R.; Philipps, P.; Farès, C.; Fürstner, A. Stabilization of a Chiral Dirhodium Carbene by Encapsulation and a Discussion of the Stereochemical Implications. Angewandte Chemie International Edition 2016, 55, 10760–10765.

Fürstner, A. Base-Metal Catalysis Marries Utilitarian Aspects with Academic Fascination. Advanced Synthesis & Catalysis 2016, 358, 2362–2363.

Tindall, D. J.; Krause, H.; Fürstner, A. Iron-Catalyzed Cross-Coupling of 1-Alkynylcyclopropyl Tosylates and Related Substrates. Advanced Synthesis & Catalysis 2016, 358, 2398–2403.

Sommer, H.; Fürstner, A. Hydroxyl-Assisted Carbonylation of Alkenyltin Derivatives: Development and Application to a Formal Synthesis of Tubelactomicin A. Organic Letters 2016, 18, 3210–3213.

Schaubach, S.; Gebauer, K.; Ungeheuer, F.; Hoffmeister, L.; Ilg, M. K.; Wirtz, C.; Fürstner, A. A Two-Component Alkyne Metathesis Catalyst System with an Improved Substrate Scope and Functional Group Tolerance: Development and Applications to Natural Product Synthesis. Chemistry – A European Journal 2016, 22, 8494–8507.

Zhuo, C.-X.; Fürstner, A. Concise Synthesis of a Pateamine A Analogue with In Vivo Anticancer Activity Based on an Iron-Catalyzed Pyrone Ring Opening/Cross-Coupling. Angewandte Chemie International Edition 2016, 55, 6051–6056.

Cromm, P. M.; Schaubach, S.; Spiegel, J.; Fürstner, A.; Grossmann, T. N.; Waldmann, H. Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides. Nature Communications 2016, 7, 11300.