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 23 (50), S. 12412 - 12419 (2017)

Wang, Y.; Lee, S.; Lam, W.; Chen, S.-R.; Dutschman, G. E.; Gullen, E. A.; Grill, S. P.; Cheng, Y.; Fürstner, A.; Francis, S. et al.; 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 7, 10037 (2017)

Casitas, A.; Rees, J. A.; Goddard, R.; Bill, E.; DeBeer, S.; Fürstner, A.: Two Exceptional Homoleptic Iron(IV) Tetraalkyl Complexes. Angewandte Chemie International Edition 56 (34), S. 10108 - 10113 (2017)

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 56 (26), S. 7525 - 7530 (2017)

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 56 (22), S. 6161 - 6165 (2017)

Debrouwer, W.; Fürstner, A.: Rearrangement of a Transient Gold Vinylidene into Gold Carbenes. Chemistry – A European Journal 23 (18), S. 4271 - 4275 (2017)

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 56 (13), S. 3599 - 3604 (2017)

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 139 (6), S. 2443 - 2455 (2017)

Sommer, H.; Fürstner, A.: Stereospecific Synthesis of Fluoroalkenes by Silver-Mediated Fluorination of Functionalized Alkenylstannanes. Chemistry – A European Journal 23 (3), S. 558 - 562 (2017)

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

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 2 (11), S. 778 - 789 (2016)

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 17 (20), S. 1915 - 1919 (2016)

Echeverria, P.-G.; Fürstner, A.: An Iron-Catalyzed Bond-Making/Bond-Breaking Cascade Merges Cycloisomerization and Cross-Coupling Chemistry. Angewandte Chemie International Edition 55 (37), S. 11188 - 11192 (2016)

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 55 (36), S. 10760 - 10765 (2016)

Fürstner, A.: Base-Metal Catalysis Marries Utilitarian Aspects with Academic Fascination. Advanced Synthesis & Catalysis 358 (15), S. 2362 - 2363 (2016)

Tindall, D. J.; Krause, H.; Fürstner, A.: Iron-Catalyzed Cross-Coupling of 1-Alkynylcyclopropyl Tosylates and Related Substrates. Advanced Synthesis & Catalysis 358 (15), S. 2398 - 2403 (2016)

Sommer, H.; Fürstner, A.: Hydroxyl-Assisted Carbonylation of Alkenyltin Derivatives: Development and Application to a Formal Synthesis of Tubelactomicin A. Organic Letters 18 (13), S. 3210 - 3213 (2016)

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 22 (25), S. 8494 - 8507 (2016)

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 55 (20), S. 6051 - 6056 (2016)

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 7, 11300 (2016)