Works matching DE "ANTI-Markovnikov reaction"
Results: 18
(Aminomethyl)pyridine Complexes for the Cobalt-Catalyzed Anti-Markovnikov Hydrosilylation of Alkoxy- or Siloxy(vinyl)silanes with Alkoxy- or Siloxyhydrosilanes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 13, p. 3665, doi. 10.1002/anie.201612460
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Aromatic Osmacyclopropenefuran Bicycles and Their Relevance for the Metal-Mediated Hydration of Functionalized Allenes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 44, p. 13749, doi. 10.1002/anie.201606839
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An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 40, p. 12295, doi. 10.1002/anie.201606832
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Biosynthetic Mechanism of Lanosterol: Cyclization.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 30, p. 8693, doi. 10.1002/anie.201501986
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- Article
Platinum(II) Olefin Hydroarylation Catalysts: Tuning Selectivity for the anti-Markovnikov Product.
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- Chemistry - A European Journal, 2014, v. 20, n. 52, p. 17287, doi. 10.1002/chem.201405174
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Development of an Improved Rhodium Catalyst for Z-Selective Anti-Markovnikov Addition of Carboxylic Acids to Terminal Alkynes.
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- Chemistry - A European Journal, 2013, v. 19, n. 36, p. 12067, doi. 10.1002/chem.201300160
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Mild Ring‐Opening 1,3‐Hydroborations of Non‐Activated Cyclopropanes.
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- Angewandte Chemie, 2018, v. 130, n. 51, p. 17103, doi. 10.1002/ange.201811036
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Ex Situ Formation of Methanethiol: Application in the Gold(I)‐Promoted Anti‐Markovnikov Hydrothiolation of Olefins.
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- Angewandte Chemie, 2018, v. 130, n. 42, p. 14083, doi. 10.1002/ange.201809051
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Alkoxyl Radicals Generated under Photoredox Catalysis: A Strategy for anti‐Markovnikov Alkoxylation Reactions.
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- Angewandte Chemie, 2018, v. 130, n. 42, p. 13986, doi. 10.1002/ange.201806522
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Aldehyde-Selective Wacker-Type Oxidation of Unbiased Alkenes Enabled by a Nitrite Co-Catalyst.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 43, p. 11257, doi. 10.1002/anie.201306756
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Theoretical study of an anti-Markovnikov addition reaction catalyzed by β-cyclodextrin.
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- Journal of Molecular Modeling, 2018, v. 24, n. 4, p. 1, doi. 10.1007/s00894-018-3595-x
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Substrate-Mediated Deactivation of a Ru(P <sup>t</sup><sup>Bu</sup><sub>2</sub>N<sup>Bn</sup><sub>2</sub>) Cooperative Complex.
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- European Journal of Inorganic Chemistry, 2015, v. 2015, n. 25, p. 4162, doi. 10.1002/ejic.201500798
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Chemoselective Alkene Hydrosilylation Catalyzed by Nickel Pincer Complexes.
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- Angewandte Chemie, 2015, v. 127, n. 48, p. 14731, doi. 10.1002/ange.201507829
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Anti-Markovnikov hydration of α-olefins and the other pathways to n-alcohols.
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- Kinetics & Catalysis, 2014, v. 55, n. 2, p. 172, doi. 10.1134/S0023158414020128
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Rhenium‐ and Manganese‐Catalyzed Selective Alkenylation of Indoles.
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- ChemCatChem, 2018, v. 10, n. 12, p. 2681, doi. 10.1002/cctc.201800553
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Hydrothiolation of Alkenes and Alkynes Catalyzed by 3,4-Dimethyl-5-vinylthiazolium iodide and Poly(3,4-dimethyl-5-vinylthiazolium) iodide.
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- ChemCatChem, 2016, v. 8, n. 15, p. 2476, doi. 10.1002/cctc.201600363
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An Iron Catalyst for Asymmetric Alkene Hydrosilylation.
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- ChemCatChem, 2015, v. 7, n. 13, p. 1918, doi. 10.1002/cctc.201500348
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Anti-Markovnikov Hydroamination of Aromatic Alkenes with Secondary Amines Catalyzed by Easily Accessible Yttrium Complexes.
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- ChemCatChem, 2014, v. 6, n. 7, p. 2065, doi. 10.1002/cctc.201402012
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- Article