Works matching AU Fürstner, Alois
Results: 292
An Efficient and Scalable "Second Generation" Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity.
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- Chemistry - A European Journal, 2024, v. 30, n. 40, p. 1, doi. 10.1002/chem.202401429
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Elucidating the Electronic Nature of Rh‐based Paddlewheel Catalysts from <sup>103</sup>Rh NMR Chemical Shifts: Insights from Quantum Mechanical Calculations.
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- Chemistry - A European Journal, 2024, v. 30, n. 4, p. 1, doi. 10.1002/chem.202301846
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Total Synthesis of the Guangnanmycin A Alcohol.
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- Angewandte Chemie, 2024, v. 136, n. 10, p. 1, doi. 10.1002/ange.202319070
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Taming of Furfurylidenes by Chiral Bismuth‐Rhodium Paddlewheel Catalysts. Preparation and Functionalization of Optically Active 1,1‐Disubstituted (Trifluoromethyl)cyclopropanes.
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- Angewandte Chemie, 2023, v. 135, n. 44, p. 1, doi. 10.1002/ange.202311598
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Chiral Bismuth‐Rhodium Paddlewheel Complexes Empowered by London Dispersion: The C−H Functionalization Nexus.
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- Angewandte Chemie, 2022, v. 134, n. 45, p. 1, doi. 10.1002/ange.202212546
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Total Synthesis of the Tetracyclic Pyridinium Alkaloid epi‐Tetradehydrohalicyclamine B.
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- Angewandte Chemie, 2022, v. 134, n. 41, p. 1, doi. 10.1002/ange.202209651
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An Anionic Dinuclear Ruthenium Dihydrogen Complex of Relevance for Alkyne gem‐Hydrogenation.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202201311
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Hydrogenative Cycloisomerization and Sigmatropic Rearrangement Reactions of Cationic Ruthenium Carbenes Formed by Catalytic Alkyne gem‐Hydrogenation.
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- Angewandte Chemie, 2022, v. 134, n. 8, p. 1, doi. 10.1002/ange.202113827
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An Alkyne‐Metathesis‐Based Approach to the Synthesis of the Anti‐Malarial Macrodiolide Samroiyotmycin A.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18652, doi. 10.1002/ange.202105732
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Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N.
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- Angewandte Chemie, 2021, v. 133, n. 14, p. 7979, doi. 10.1002/ange.202016477
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Total Synthesis of Mycinolide IV and Path‐Scouting for Aldgamycin N.
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- Angewandte Chemie, 2021, v. 133, n. 14, p. 7972, doi. 10.1002/ange.202016475
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Collective Total Synthesis of Casbane Diterpenes: One Strategy, Multiple Targets.
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- Angewandte Chemie, 2021, v. 133, n. 10, p. 5376, doi. 10.1002/ange.202015243
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The Formosalides: Structure Determination by Total Synthesis.
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- Angewandte Chemie, 2021, v. 133, n. 1, p. 450, doi. 10.1002/ange.202011472
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<sup>183</sup>W NMR Spectroscopy Guides the Search for Tungsten Alkylidyne Catalysts for Alkyne Metathesis.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21942, doi. 10.1002/ange.202009975
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Grubbs Metathesis Enabled by a Light‐Driven gem‐Hydrogenation of Internal Alkynes.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18581, doi. 10.1002/ange.202007030
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A Heteroleptic Dirhodium Catalyst for Asymmetric Cyclopropanation with α‐Stannyl α‐Diazoacetate. "Stereoretentive" Stille Coupling with Formation of Chiral Quarternary Carbon Centers.
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- Angewandte Chemie, 2020, v. 132, n. 33, p. 14004, doi. 10.1002/ange.202004377
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Modular Synthesis of Furans with up to Four Different Substituents by a trans‐Carboboration Strategy.
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- Angewandte Chemie, 2020, v. 132, n. 32, p. 13720, doi. 10.1002/ange.202005560
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Walter Thiel (1949–2019).
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- Angewandte Chemie, 2020, v. 132, n. 4, p. 1398, doi. 10.1002/ange.201915463
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Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem‐Hydrogenation or through Carbophilic Activation of Alkynes.
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- Angewandte Chemie, 2019, v. 131, n. 51, p. 18647, doi. 10.1002/ange.201912161
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Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts.
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- Angewandte Chemie, 2019, v. 131, n. 44, p. 15837, doi. 10.1002/ange.201908571
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Hydrogenative Cyclopropanation and Hydrogenative Metathesis.
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- Angewandte Chemie, 2019, v. 131, n. 26, p. 8943, doi. 10.1002/ange.201904256
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Alkyne gem‐Hydrogenation: Formation of Pianostool Ruthenium Carbene Complexes and Analysis of Their Chemical Character.
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- Angewandte Chemie, 2019, v. 131, n. 26, p. 8937, doi. 10.1002/ange.201904255
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Gold Difluorocarbenoid Complexes: Spectroscopic and Chemical Profiling.
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- Angewandte Chemie, 2019, v. 131, n. 26, p. 8926, doi. 10.1002/ange.201903957
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Chiral Heterobimetallic Bismuth–Rhodium Paddlewheel Catalysts: A Conceptually New Approach to Asymmetric Cyclopropanation.
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- Angewandte Chemie, 2019, v. 131, n. 11, p. 3595, doi. 10.1002/ange.201900265
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Metathesis at an Implausible Site: A Formal Total Synthesis of Rhizoxin D.
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- Angewandte Chemie, 2019, v. 131, n. 1, p. 254, doi. 10.1002/ange.201812096
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Collective and Diverted Total Synthesis of the Strasseriolides: A Family of Macrolides Endowed with Potent Antiplasmodial and Antitrypanosomal Activity.
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- Angewandte Chemie, 2024, v. 136, n. 36, p. 1, doi. 10.1002/ange.202408725
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DMDA-PatA mediates RNA sequence-selective translation repression by anchoring eIF4A and DDX3 to GNG motifs.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51635-9
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Total Synthesis of Neurymenolide A Based on a Gold-Catalyzed Synthesis of 4-Hydroxy-2-pyrones.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 28, p. 6929, doi. 10.1002/anie.201203180
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Total Synthesis of Tulearin C.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 48, p. 11373, doi. 10.1002/anie.201106117
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Second-Generation Total Synthesis of Spirastrellolide F Methyl Ester: The Alkyne Route.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 37, p. 8739, doi. 10.1002/anie.201103270
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Rendering Schrock-type Molybdenum Alkylidene Complexes Air Stable: User-Friendly Precatalysts for Alkene Metathesis.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 34, p. 7829, doi. 10.1002/anie.201102012
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The Leiodolide B Puzzle.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 1, p. 304, doi. 10.1002/anie.201005850
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Elementary Steps in Gold Catalysis: The Significance of gem-Diauration.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 45, p. 8466, doi. 10.1002/anie.201003349
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Steering the Surprisingly Modular π-Acceptor Properties of N-Heterocyclic Carbenes: Implications for Gold Catalysis.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 14, p. 2542, doi. 10.1002/anie.200907194
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Enantioselective Gold Catalysis: Opportunities Provided by Monodentate Phosphoramidite Ligands with an Acyclic TADDOL Backbone.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 11, p. 1949, doi. 10.1002/anie.200906550
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Total Synthesis of Spirastrellolide F Methyl Ester-Part 2: Macrocyclization and Completion of the Synthesis.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 52, p. 9946, doi. 10.1002/anie.200906122
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Total Synthesis of Spirastrellolide F Methyl Ester-Part 1: Strategic Considerations and Revised Approach to the Southern Hemisphere.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 52, p. 9940, doi. 10.1002/anie.200906121
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Elementary Steps of Gold Catalysis: NMR Spectroscopy Reveals the Highly Cationic Character of a 'Gold Carbenoid'.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 14, p. 2510, doi. 10.1002/anie.200806059
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From Oblivion into the Limelight: Iron (Domino) Catalysis.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 8, p. 1364, doi. 10.1002/anie.200805728
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A Synthesis-Driven Structure Revision of Berkelic Acid Methyl Ester.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 44, p. 8450, doi. 10.1002/anie.200803339
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Carbenes Stabilized by Ylides: Pushing the Limits.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 43, p. 8302, doi. 10.1002/anie.200803200
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On the Nature of the Reactive Intermediates in Gold-Catalyzed Cycloisomerization Reactions.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 27, p. 5030, doi. 10.1002/anie.200800934
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Coordination Chemistry of Ene-1,1-diamines and a Prototype 'Carbodicarbene'.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 17, p. 3210, doi. 10.1002/anie.200705798
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Total Syntheses of Amphidinolide H and G.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 48, p. 9265, doi. 10.1002/anie.200704024
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Concise Total Synthesis of Cruentaren A.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 48, p. 9275, doi. 10.1002/anie.200703839
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Two Manifolds for Metal-Catalyzed Intramolecular Diels-Alder Reactions of Unactivated Alkynes.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 46, p. 8845, doi. 10.1002/anie.200703321
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What is Amphidinolide V? Report on a Likely Conquest.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 29, p. 5545, doi. 10.1002/anie.200701640
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Total Synthesis of the Antibiotic Erypoegin H and Cognates by a PtCl.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 25, p. 4760, doi. 10.1002/anie.200700895
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Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 19, p. 3410, doi. 10.1002/anie.200604335
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Total Synthesis of Iejimalide BGenerous financial support from the MPG, the Fonds der Chemischen Industrie, the Alexander-von-Humboldt Foundation (fellowship to C.N.), the NSERC Canada (fellowship to M.T.), and the Austrian Fonds zur Förderung der Wissenschaftlichen Forschung (fellowship to M.W.) is gratefully acknowledged. We thank Dr. R. Mynott, B. Gabor, and C. Wirtz for their invaluable help with the structure assignment of several key compounds, and R. Leichtweiß for HPLC assistance.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 35, p. 5837
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