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Stabilization of a Chiral Dirhodium Carbene by Encapsulation and a Discussion of the Stereochemical Implications.
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- Angewandte Chemie, 2016, v. 128, n. 36, p. 10918, doi. 10.1002/ange.201605502
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Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation.
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- Angewandte Chemie, 2015, v. 127, n. 42, p. 12608, doi. 10.1002/ange.201506075
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Innentitelbild: Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation (Angew. Chem. 42/2015).
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- Angewandte Chemie, 2015, v. 127, n. 42, p. 12348, doi. 10.1002/ange.201508274
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Simultaneous Determination of the Conformation and Relative Configuration of Archazolide A by Using Nuclear Overhauser Effects, J Couplings, and Residual Dipolar Couplings.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 20, p. 3722, doi. 10.1002/anie.200800225
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An Atom-Economical and Stereoselective Domino Synthesis of Functionalised Dienes.
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- Chemistry - A European Journal, 2013, v. 19, n. 21, p. 6566, doi. 10.1002/chem.201300776
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Synthesis and Structure of Carbene-Stabilized N-Centered Cations [L<sub>2</sub>N]<sup>+</sup>, [L<sub>2</sub>NR]<sup>2+</sup>, [LNR<sub>3</sub>]<sup>2+</sup>, and [L<sub>3</sub>N]<sup>3+</sup>.
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- Chemistry - A European Journal, 2013, v. 19, n. 11, p. 3542, doi. 10.1002/chem.201204186
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Conformational Investigations in Flexible Molecules Using Orientational NMR Constraints in Combination with 3J-Couplings and NOE Distances.
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- Molecules, 2019, v. 24, n. 23, p. 4417, doi. 10.3390/molecules24234417
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Stabilization of a Chiral Dirhodium Carbene by Encapsulation and a Discussion of the Stereochemical Implications.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 36, p. 10760, doi. 10.1002/anie.201605502
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- Article
Inside Cover: Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation (Angew. Chem. Int. Ed. 42/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 42, p. 12180, doi. 10.1002/anie.201508274
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- Publication type:
- Article
Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 42, p. 12431, doi. 10.1002/anie.201506075
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- Article
Chemoselective Intermolecular α-Arylation of Amides.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 21, p. 5462, doi. 10.1002/anie.201402229
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Palladium-Catalyzed Allylic Substitution at Four-Membered-Ring Systems: Formation of η<sup>1</sup>-Allyl Complexes and Electrocyclic Ring Opening.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 24, p. 6313, doi. 10.1002/anie.201301034
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Side-Chain Orientation and Hydrogen-Bonding Imprint Supra-tc Motion on the Protein Backbone of Ubiquitin.
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- Angewandte Chemie, 2005, v. 117, n. 47, p. 7954, doi. 10.1002/ange.200502573
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A multi-substrate screening approach for the identification of a broadly applicable Diels-Alder catalyst.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08374-z
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Inside Cover: A Cooperative Rhodium/Secondary Phosphine Oxide [Rh/P(O)nBu<sub>2</sub>] Template for Catalytic Hydrodefluorination of Perfluoroarenes (Angew. Chem. Int. Ed. 23/2023).
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- Angewandte Chemie International Edition, 2023, v. 62, n. 23, p. 1, doi. 10.1002/anie.202303992
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- Article
A Cooperative Rhodium/Secondary Phosphine Oxide [Rh/P(O)nBu<sub>2</sub>] Template for Catalytic Hydrodefluorination of Perfluoroarenes.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 23, p. 1, doi. 10.1002/anie.202219127
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An Adaptive Rhodium Catalyst to Control the Hydrogenation Network of Nitroarenes.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 36, p. 1, doi. 10.1002/anie.202205515
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Chemoselektive intermolekulare α-Arylierung von Amiden.
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- Angewandte Chemie, 2014, v. 126, n. 21, p. 5566, doi. 10.1002/ange.201402229
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- Article
Palladium-katalysierte allylische Substitution an viergliedrigen Ringen: Bildung von η<sup>1</sup>-Allylkomplexen und elektrocyclische Ringöffnung.
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- Angewandte Chemie, 2013, v. 125, n. 24, p. 6434, doi. 10.1002/ange.201301034
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A novel strategy for NMR resonance assignment and protein structure determination.
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- Journal of Biomolecular NMR, 2011, v. 49, n. 1, p. 27, doi. 10.1007/s10858-010-9458-0
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Accessing ns–μs side chain dynamics in ubiquitin with methyl RDCs.
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- Journal of Biomolecular NMR, 2009, v. 45, n. 1/2, p. 23, doi. 10.1007/s10858-009-9354-7
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Self-consistent residual dipolar coupling based model-free analysis for the robust determination of nanosecond to microsecond protein dynamics.
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- Journal of Biomolecular NMR, 2008, v. 41, n. 3, p. 139, doi. 10.1007/s10858-008-9244-4
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NMReDATA: Tools and applications.
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- Magnetic Resonance in Chemistry, 2021, v. 59, n. 8, p. 782, doi. 10.1002/mrc.5146
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Cromolyn/gelatin mixtures as aqueous alignment media and utilization of their mechanical stability for a layering technique.
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- Magnetic Resonance in Chemistry, 2018, v. 56, n. 12, p. 1176, doi. 10.1002/mrc.4786
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NMReDATA, a standard to report the NMR assignment and parameters of organic compounds.
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- Magnetic Resonance in Chemistry, 2018, v. 56, n. 8, p. 703, doi. 10.1002/mrc.4737
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Solution NMR structure of an immunodominant epitope of myelin basic protein.
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- FEBS Journal, 2006, v. 273, n. 3, p. 601, doi. 10.1111/j.1742-4658.2005.05093.x
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A Striking Case of Enantioinversion in Gold Catalysis and Its Probable Origins.
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- Chemistry - A European Journal, 2015, v. 21, n. 35, p. 12279, doi. 10.1002/chem.201502160
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Transient structure and dynamics in the disordered c-Myc transactivation domain affect Bin1 binding.
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- Nucleic Acids Research, 2012, v. 40, n. 13, p. 6353, doi. 10.1093/nar/gks263
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Structural Insight into the Complex of Ferredoxin and [FeFe] Hydrogenase from Chlamydomonas reinhardtii.
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- ChemBioChem, 2015, v. 16, n. 11, p. 1663, doi. 10.1002/cbic.201500130
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Cover Picture: Expedited Synthesis of Metal Phosphides Maximizes Dispersion, Air Stability, and Catalytic Performance in Selective Hydrogenation (Angew. Chem. Int. Ed. 33/2024).
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- Angewandte Chemie International Edition, 2024, v. 63, n. 33, p. 1, doi. 10.1002/anie.202411602
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Expedited Synthesis of Metal Phosphides Maximizes Dispersion, Air Stability, and Catalytic Performance in Selective Hydrogenation.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 33, p. 1, doi. 10.1002/anie.202404292
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- Article
Titelbild: Expedited Synthesis of Metal Phosphides Maximizes Dispersion, Air Stability, and Catalytic Performance in Selective Hydrogenation (Angew. Chem. 33/2024).
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- Angewandte Chemie, 2024, v. 136, n. 33, p. 1, doi. 10.1002/ange.202411602
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- Article
Expedited Synthesis of Metal Phosphides Maximizes Dispersion, Air Stability, and Catalytic Performance in Selective Hydrogenation.
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- Angewandte Chemie, 2024, v. 136, n. 33, p. 1, doi. 10.1002/ange.202404292
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- Publication type:
- Article
Innentitelbild: Ein Kooperatives Rhodium/Sekundäres Phosphinoxid [Rh/P(O)nBu<sub>2</sub>]‐Template zur Katalytischen Hydrodefluorierung von Perfluoroarenen (Angew. Chem. 23/2023)
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- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202219127
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- Article
Innentitelbild: Ein Kooperatives Rhodium/Sekundäres Phosphinoxid [Rh/P(O)nBu<sub>2</sub>]‐Template zur Katalytischen Hydrodefluorierung von Perfluoroarenen (Angew. Chem. 23/2023).
- Published in:
- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202219127
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- Publication type:
- Article
Ein Kooperatives Rhodium/Sekundäres Phosphinoxid [Rh/P(O)nBu<sub>2</sub>]‐Template zur Katalytischen Hydrodefluorierung von Perfluoroarenen.
- Published in:
- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202219127
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- Article
Ein adaptiver Rhodiumkatalysator zur Steuerung des Hydrierungsnetzwerks von Nitroarenen.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202205515
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1D and 2D NMR Spectroscopy of Bonding Interactions within Stable and Phase-Separating Organic Electrolyte-Cellulose Solutions.
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- ChemSusChem, 2017, v. 10, n. 17, p. 3452, doi. 10.1002/cssc.201701042
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Side-Chain Orientation and Hydrogen-Bonding Imprint Supra-τc Motion on the Protein Backbone of UbiquitinThis work was supported by the MPG, the DFG, and the Fonds der Chemischen Industrie (to C.G.). We thank Dirk Lennartz (Bayer Leverkusen), Vinesh Vijayan, and Karel Kubicek (both MPI Göttingen) for useful discussions and help with the measurement of dipolar couplings used for this analysis, and Karin Giller for expert technical help expressing ubiquitin. Nico Tjandra (NIH, Washington) kindly provided Lipari–Szabo order parameters of backbone amide groups at 35 °C. J.M. thanks the Human Frontier Science Program (HFSP) for financial support.
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- Angewandte Chemie International Edition, 2005, v. 44, n. 47, p. 7776, doi. 10.1002/anie.200502573
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- Article