Chemistry for me
Publications
Fluoride Additive as a Simple Tool to Qualitatively Improve Performance of Nickel-Catalyzed Asymmetric Michael Addition of Malonates to Nitroolefins
Borrowing hydrogen amination: Whether a catalyst is required?
J. Catal., 2022; 413, 2022, 1070-1076, Impact Factor: 7.92
Borrowing Hydrogen Amination Reactions: A Complex Analysis of Trends and Correlations of the Various Reaction Parameters
Asymmetric cyclopropanation of electron-rich alkenes by the racemic diene rhodium catalyst: the chiral poisoning approach
Syngas Instead of Hydrogen Gas as a Reducing Agent─ A Strategy To Improve the Selectivity and Efficiency of Organometallic Catalysts
Enhancing the efficiency of the ruthenium catalysts in the reductive amination without an external hydrogen source
J. Catal., 2021; 405, 2022, 404-409, Impact Factor: 7.92
Synthesis of Rhodium Complexes with Chiral Diene Ligands via Diastereoselective Coordination and Their Application in the Asymmetric Insertion of Diazo Compounds into E−H Bonds
Angew. Chem., 2021, 60, 34, 18712-18720, Impact Factor: 15.336
Straightforward Access to High-Performance Organometallic Catalysts by Fluoride Activation: Proof of Principle on Asymmetric Cyanation, Asymmetric Michael Addition, CO2 Addition to Epoxide, and Reductive Alkylation of Amines by Tetrahydrofuran
ACS Cat., 2021, 11, 13077-13084, Impact Factor: 13.084
Hayashi ligand-based rhodium complex in carbon monoxide and molecular hydrogen-assisted reductive amination
Mend. Commun., 2021; 31 (6), 781-783, Impact Factor: 1.694
Frontispiece: Reductive Aldol-type Reactions in the Synthesis of Pharmaceuticals
Phosphine ligands in the ruthenium-catalyzed reductive amination without an external hydrogen source
J. Organomet. Chem., 2021; 941, 121806, Impact Factor: 2.369
Reductive Aldol-type Reactions in the Synthesis of Pharmaceuticals
Easy Access to Versatile Catalytic Systems for C−H Activation and Reductive Amination Based on Tetrahydrofluorenyl Rhodium(III) Complexes
Chem. Eur. J., 2021, 27, 42, 10903-10912, Impact Factor: 5.236
Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power
Catal. Sci. Technol., 2021,11, 4922-4930, Impact Factor: 6.119
Eur. J. Organ. Chem., 2021; 4, 543-586, Impact Factor: 2.889
Reductive Amidation without an External Hydrogen Source Using Rhodium on Carbon Matrix as a Catalyst
ChemCatChem, 2020, 12, 1, 112-117, Impact Factor: 5.686
A Dual Threat: Redox‐Activity and Electronic Structures of Well‐Defined Donor–Acceptor Fulleretic Covalent‐Organic Materials
Angew. Chem., 2020, 59, 15, 6000-6006, Impact Factor: 15.336
Redox Condensations of o-Nitrobenzaldehydes with Amines under Mild Conditions: Total Synthesis of the Vasicinone Family
J. Org. Chem. 2020, 85, 14, 9347–9360, Impact Factor: 4.335
Direct Reductive Amination of Camphor Using Iron Pentacarbonyl as Stoichiometric Reducing Agent: Features and Limitations
Eur. J. Organ. Chem., 2020; 38, 6289-6294, Impact Factor: 2.889
Rhodium‐Catalyzed Reductive Esterification Using Carbon Monoxide as a Reducing Agent
Eur. J. Organ. Chem., 2020, 27, 4116-4121 Impact Factor: 2.889
Tris(pyrazolyl)borate rhodium complexes. Application for reductive amination and esterification of aldehydes in the presence of carbon monoxide
J. Organomet. Chem., 2020, 925, 121468, Impact Factor: 2.369
Anthracene–rhodium complexes with metal coordination at the central ring – a new class of catalysts for reductive amination
Org. Biomol. Chem., 2019, 17, 1, 83-87, Impact Factor: 3.876
Synthesis of Nitriles from Aldehydes with Elongation of the Molecule with Two Carbon Atoms
Eur. J. Organ. Chem., 2019, 1, 32-35, Impact factor: 2.889
Fluorene Complexes of Group 9 Metals: Fluorene Effect and Application for Reductive Amination
Organometal., 2019, 38, 16, 3151–3158, Impact Factor: 3.876
One‐Pot Synthesis of Symmetrical Tertiary and Secondary Amines from Carbonyl Compounds, Ammonium Carbonate and Carbon Monoxide as a Reductant
Eur. J. Organ. Chem., 2019; 38, 6557-6560, Impact Factor: 2.889
Reductive Amination in the Synthesis of Pharmaceuticals
Chem. Rev. 2019, 119, 23, 11857–11911, Impact Factor: 52.758
Aldehydes as Alkylating Agents for Ketones
Chem. Eur. J., 2019, 25, 71, 16225-16229, Impact Factor: 5.236
Reduction of phosphine oxides to phosphines
Tetrahed. Lett., 2019, 60, 8, 575-582, Impact Factor: 2.415
Dichotomy of Atom-Economical Hydrogen-Free Reductive Amidation vs Exhaustive Reductive Amination
Org. Lett., 2017, 19, 20, 5657–5660, Impact Factor: 6.005
Planar‐chiral rhodium(III) catalyst with sterically demanding cyclopentadienyl ligand and its application for enantioselective synthesis of dihydroisoquinolones
Angew. Chem. Int. Ed., 2018, 57, 26, 7904-7904, Impact Factor: 15.336
Synthesis of N,N′-Dialkylated Cyclohexane-1,2-diamines and Their Application as Asymmetric Ligands and Organocatalysts for the Synthesis of Alcohols
Synl. , 2017, 28, 05, 615-619, Impact Factor: 2.006
Hydrogen-Free Reductive Amination Using Iron Pentacarbonyl as a Reducing Agent
Org. Biomol. Chem., 2017, 15, 10164–10166, Impact Factor: 3.412
The synthesis of sterically hindered amines by a direct reductive amination of ketones
Chem. Commun., 2016, 52, 1397-1400, Impact Factor: 5.996
Cyclobutadiene Metal Complexes: A New Class of Highly Selective Catalysts. An Application to Direct Reductive Amination
ACS Cat., 2016, 6, 3, 2043–2046, Impact Factor: 13.084
Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source
Org. Lett., 2015, 17, 2, 173–175, Impact Factor: 6.005
Reductive Transformations of Carbonyl Compounds Catalyzed by Rhodium Supported on a Carbon Matrix by using Carbon Monoxide as a Deoxygenative Agent.
ChemCatChem, 2015, 7, 2590–2593, Impact Factor: 5.686
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