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Synthesis of Carboxylic Acids by Palladium‐Catalyzed Hydroxycarbonylation.
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- Angewandte Chemie, 2019, v. 131, n. 40, p. 14503, doi. 10.1002/ange.201908451
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- Article
Palladium-Catalyzed Carbonylation of sec- and tert-Alcohols.
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- Angewandte Chemie, 2017, v. 129, n. 22, p. 6299, doi. 10.1002/ange.201701950
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- Article
Carbonylierungen mit CO<sub>2</sub> als CO-Quelle und Reaktivitätsmodifikator.
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- Angewandte Chemie, 2017, v. 129, n. 20, p. 5485, doi. 10.1002/ange.201702292
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- Article
Efficient Palladium-Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands.
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- Angewandte Chemie, 2017, v. 129, n. 19, p. 5351, doi. 10.1002/ange.201700317
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- Article
Innentitelbild: Efficient Palladium-Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands (Angew. Chem. 19/2017).
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- Angewandte Chemie, 2017, v. 129, n. 19, p. 5216, doi. 10.1002/ange.201702485
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- Article
Copper-Catalyzed Carbonylative Coupling of Cycloalkanes and Amides.
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- Angewandte Chemie, 2016, v. 128, n. 25, p. 7343, doi. 10.1002/ange.201603235
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- Article
Palladium-Catalyzed Hydroamidocarbonylation of Olefins to Imides.
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- Angewandte Chemie, 2015, v. 127, n. 35, p. 10377, doi. 10.1002/ange.201503954
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- Article
Highly active and efficient catalysts for alkoxycarbonylation of alkenes.
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- Nature Communications, 2017, v. 8, n. 1, p. 14117, doi. 10.1038/ncomms14117
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- Article
Selective catalytic two-step process for ethylene glycol from carbon monoxide.
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- Nature Communications, 2016, v. 7, n. 7, p. 12075, doi. 10.1038/ncomms12075
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- Article
Efficient Synthesis of γ‐Lactones by Cobalt‐Catalyzed Carbonylative Ring Expansion of Oxetanes under Syngas Atmosphere.
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- ChemCatChem, 2020, v. 12, n. 23, p. 5898, doi. 10.1002/cctc.202001294
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- Article
Palladium-Catalyzed Carbonylation of sec- and tert-Alcohols.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 22, p. 6203, doi. 10.1002/anie.201701950
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- Article
Carbonylations with CO<sub>2</sub> as the CO Source and Reactivity Modifier.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 20, p. 5399, doi. 10.1002/anie.201702292
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- Publication type:
- Article
Efficient Palladium-Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 19, p. 5267, doi. 10.1002/anie.201700317
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- Article
Inside Cover: Efficient Palladium-Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands (Angew. Chem. Int. Ed. 19/2017).
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- Angewandte Chemie International Edition, 2017, v. 56, n. 19, p. 5134, doi. 10.1002/anie.201702485
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- Publication type:
- Article
Copper-Catalyzed Carbonylative Coupling of Cycloalkanes and Amides.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 25, p. 7227, doi. 10.1002/anie.201603235
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- Publication type:
- Article
Palladium-Catalyzed Hydroamidocarbonylation of Olefins to Imides.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 35, p. 10239, doi. 10.1002/anie.201503954
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- Article
Catalytic Asymmetric Hydrogenation of α-CF<sub>3</sub>- or β-CF<sub>3</sub>-Substituted Acrylic Acids using Rhodium(I) Complexes with a Combination of Chiral and Achiral Ligands.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 52, p. 14191, doi. 10.1002/anie.201307903
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- Article
Rhodium(I)-Catalyzed Enantioselective Hydrogenation of Substituted Acrylic Acids with Sterically Similar β,β-Diaryls.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 26, p. 6748, doi. 10.1002/anie.201302349
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- Article
Diastereoselective Alkene Hydroesterification Enabling the Synthesis of Chiral Fused Bicyclic Lactones.
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- Chemistry - A European Journal, 2021, v. 27, n. 72, p. 18039, doi. 10.1002/chem.202103318
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- Article
Pairing Electrocarboxylation of Unsaturated Bonds with Oxidative Transformation of Alcohol and Amine.
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- ChemSusChem, 2023, v. 16, n. 19, p. 1, doi. 10.1002/cssc.202300807
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- Article
Asymmetric Double Hydroxycarbonylation of Alkynes to Chiral Succinic Acids Enabled by Palladium Relay Catalysis.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 29, p. 1, doi. 10.1002/anie.202204156
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- Article
Asymmetric Alkoxy‐ and Hydroxy‐Carbonylations of Functionalized Alkenes Assisted by β‐Carbonyl Groups.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 32, p. 17693, doi. 10.1002/anie.202105977
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- Article
Synthesis of Carboxylic Acids by Palladium‐Catalyzed Hydroxycarbonylation.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 40, p. 14365, doi. 10.1002/anie.201908451
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- Publication type:
- Article
Catalytic Asymmetric Hydrogenation of α-CF<sub>3</sub>- or β-CF<sub>3</sub>-Substituted Acrylic Acids using Rhodium(I) Complexes with a Combination of Chiral and Achiral Ligands.
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- Angewandte Chemie, 2013, v. 125, n. 52, p. 14441, doi. 10.1002/ange.201307903
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- Publication type:
- Article
Rhodium(I)-Catalyzed Enantioselective Hydrogenation of Substituted Acrylic Acids with Sterically Similar β,β-Diaryls.
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- Angewandte Chemie, 2013, v. 125, n. 26, p. 6880, doi. 10.1002/ange.201302349
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- Article
Efficient Domino Hydroformylation/Benzoin Condensation: Highly Selective Synthesis of α-Hydroxy Ketones.
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- Chemistry - A European Journal, 2015, v. 21, n. 50, p. 18033, doi. 10.1002/chem.201502982
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- Article
Hydroxyl Group‐Enabled Highly Efficient Ligand for Pd‐Catalyzed Telomerization of 1,3‐Butadiene with CO<sub>2</sub>.
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- Chinese Journal of Chemistry, 2022, v. 40, n. 23, p. 2734, doi. 10.1002/cjoc.202200387
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- Article
Dual Roles of Co<sub>2</sub>(CO)<sub>8</sub> Enable Carbonylative Ring Expansion of Thietane under Ambient CO Pressure.
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- ChemistrySelect, 2021, v. 6, n. 48, p. 13964, doi. 10.1002/slct.202103878
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- Article
Asymmetric Double Hydroxycarbonylation of Alkynes to Chiral Succinic Acids Enabled by Palladium Relay Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202204156
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- Article
Asymmetric Alkoxy‐ and Hydroxy‐Carbonylations of Functionalized Alkenes Assisted by β‐Carbonyl Groups.
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- Angewandte Chemie, 2021, v. 133, n. 32, p. 17834, doi. 10.1002/ange.202105977
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- Article
Ring‐Opening Intramolecular Arylation of 1,2‐Disubtituted Epoxides with Tuneable Stereoselectivity.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 9, p. 1, doi. 10.1002/ejoc.202301271
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- Article