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Mechanical‐Force‐Induced Non‐spontaneous Dehalogenative Deuteration of Aromatic Iodides Enabled by Using Piezoelectric Materials as a Redox Catalyst.
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- Angewandte Chemie, 2024, v. 136, n. 28, p. 1, doi. 10.1002/ange.202400645
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Mechanical‐Force‐Induced Non‐spontaneous Dehalogenative Deuteration of Aromatic Iodides Enabled by Using Piezoelectric Materials as a Redox Catalyst.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 28, p. 1, doi. 10.1002/anie.202400645
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- Article
Catalytic Asymmetric Cascade Dearomatization of Indoles via a Photoinduced Pd‐Catalyzed 1,2‐Bisfunctionalization of Butadienes.
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202404388
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Catalytic Asymmetric Cascade Dearomatization of Indoles via a Photoinduced Pd‐Catalyzed 1,2‐Bisfunctionalization of Butadienes.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 26, p. 1, doi. 10.1002/anie.202404388
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Discovery and substrate specificity engineering of nucleotide halogenases.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49147-7
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Identifying Residues for Substrate Recognition in Human GPAT4 by Molecular Dynamics Simulations.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 7, p. 3729, doi. 10.3390/ijms25073729
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- Article
Palladium‐Catalyzed Alkyne Hydrocyanation toward Ligand‐Controlled Stereodivergent Synthesis of (E)‐ and (Z)‐Trisubstituted Acrylonitriles.
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- Angewandte Chemie, 2023, v. 135, n. 26, p. 1, doi. 10.1002/ange.202304543
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- Article
Palladium‐Catalyzed Alkyne Hydrocyanation toward Ligand‐Controlled Stereodivergent Synthesis of (E)‐ and (Z)‐Trisubstituted Acrylonitriles.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 26, p. 1, doi. 10.1002/anie.202304543
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- Article
Nickel‐Catalyzed Migratory Hydrocyanation of Internal Alkenes: Unexpected Diastereomeric‐Ligand‐Controlled Regiodivergence.
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- Angewandte Chemie, 2021, v. 133, n. 4, p. 1911, doi. 10.1002/ange.202011231
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- Article
Nickel‐Catalyzed Migratory Hydrocyanation of Internal Alkenes: Unexpected Diastereomeric‐Ligand‐Controlled Regiodivergence.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 4, p. 1883, doi. 10.1002/anie.202011231
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- Article
Computational exploration of copper catalyzed vinylogous aerobic oxidation of unsaturated compounds.
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- Scientific Reports, 2021, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-80188-2
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Mechanism for the reactivation of the peroxidase activity of human cyclooxygenases: investigation using phenol as a reducing cosubstrate.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71237-x
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- Article
Highly Regio‐ and Stereoselective Ni‐Catalyzed Hydrocyanation of 1,3‐Enynes.
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- Chemistry - A European Journal, 2020, v. 26, n. 27, p. 5956, doi. 10.1002/chem.202000651
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- Article
Molecular dynamics study of taxadiene synthase catalysis.
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- Journal of Computational Chemistry, 2018, v. 39, n. 19, p. 1215, doi. 10.1002/jcc.25184
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Catalytic Reductive Pinacol-Type Rearrangement of Unactivated 1,2-Diols through a Concerted, Stereoinvertive Mechanism.
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- Angewandte Chemie, 2017, v. 129, n. 43, p. 13562, doi. 10.1002/ange.201704936
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- Article
Catalytic Reductive Pinacol-Type Rearrangement of Unactivated 1,2-Diols through a Concerted, Stereoinvertive Mechanism.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 43, p. 13377, doi. 10.1002/anie.201704936
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- Article
Berichtigung: Hydroxy-Directed Ruthenium-Catalyzed Alkene/Alkyne Coupling: Increased Scope, Stereochemical Implications, and Mechanistic Rationale.
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- Angewandte Chemie, 2017, v. 129, n. 21, p. 5744, doi. 10.1002/ange.201703197
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Corrigendum: Hydroxy-Directed Ruthenium-Catalyzed Alkene/Alkyne Coupling: Increased Scope, Stereochemical Implications, and Mechanistic Rationale.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 21, p. 5652, doi. 10.1002/anie.201703197
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- Article
Hydroxy-Directed Ruthenium-Catalyzed Alkene/Alkyne Coupling: Increased Scope, Stereochemical Implications, and Mechanistic Rationale.
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- Angewandte Chemie, 2017, v. 129, n. 13, p. 3653, doi. 10.1002/ange.201700342
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- Article
Hydroxy-Directed Ruthenium-Catalyzed Alkene/Alkyne Coupling: Increased Scope, Stereochemical Implications, and Mechanistic Rationale.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 13, p. 3599, doi. 10.1002/anie.201700342
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- Article
A Combined IM-MS/DFT Study on [Pd(MPAA)]-Catalyzed Enantioselective C-H Activation: Relay of Chirality through a Rigid Framework.
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- Chemistry - A European Journal, 2015, v. 21, n. 31, p. 11180, doi. 10.1002/chem.201501123
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Enantioselective Formation of Cyano-Bearing All-Carbon Quaternary Stereocenters: Desymmetrization by Copper-Catalyzed N-Arylation.
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- Angewandte Chemie, 2014, v. 126, n. 36, p. 9709, doi. 10.1002/ange.201405575
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- Article
Enantioselective Formation of Cyano-Bearing All-Carbon Quaternary Stereocenters: Desymmetrization by Copper-Catalyzed N-Arylation.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 36, p. 9555, doi. 10.1002/anie.201405575
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Computational Studies on the Mechanism of the Copper-Catalyzed sp<sup>3</sup>-CH Cross-Dehydrogenative Coupling Reaction.
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- ChemPlusChem, 2013, v. 78, n. 9, p. 943, doi. 10.1002/cplu.201300117
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Silicon-Containing Formal 4π-Electron Four-Membered Ring Systems: Antiaromatic, Aromatic, or Nonaromatic?
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- Chemistry - A European Journal, 2012, v. 18, n. 24, p. 7516, doi. 10.1002/chem.201103443
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- Article