Publications

Fluoride Additive as a Simple Tool to Qualitatively Improve Performance of Nickel-Catalyzed Asymmetric Michael Addition of Malonates to Nitroolefins

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Borrowing hydrogen amination: Whether a catalyst is required?

J. Catal., 2022; 413, 2022, 1070-1076, Impact Factor: 7.92

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Borrowing Hydrogen Amination Reactions: A Complex Analysis of Trends and Correlations of the Various Reaction Parameters

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Asymmetric cyclopropanation of electron-rich alkenes by the racemic diene rhodium catalyst: the chiral poisoning approach

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Syngas Instead of Hydrogen Gas as a Reducing Agent─ A Strategy To Improve the Selectivity and Efficiency of Organometallic Catalysts

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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

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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

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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

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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

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Frontispiece: Reductive Aldol-type Reactions in the Synthesis of Pharmaceuticals

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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

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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

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Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power

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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

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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

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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 

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Variability of Rhodium(III)-Catalyzed Reactions of Aromatic Oximes with Alkenes

Synl., 2020; 31, 11, 1117-1120, Impact Factor: 2.006

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Alkyl formates as reagents for reductive amination of carbonyl compounds

Mend. Commun., 2020, 30, 1, 112-113, Impact Factor: 1.694

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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

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Rhodium‐Catalyzed Reductive Esterification Using Carbon Monoxide as a Reducing Agent

Eur. J. Organ. Chem., 2020, 27, 4116-4121 Impact Factor:  2.889

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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

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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

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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

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Fluorene Complexes of Group 9 Metals: Fluorene Effect and Application for Reductive Amination

Organometal., 2019, 38, 16, 3151–3158, Impact Factor: 3.876

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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

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Reductive Amination in the Synthesis of Pharmaceuticals

Chem. Rev. 2019, 119, 23, 11857–11911, Impact Factor:  52.758

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Aldehydes as Alkylating Agents for Ketones

Chem. Eur. J., 2019, 25, 71, 16225-16229, Impact Factor: 5.236

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Reduction of phosphine oxides to phosphines

Tetrahed. Lett., 2019, 60, 8, 575-582, Impact Factor: 2.415

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Atom- and Step-Economical Ruthenium-Catalyzed Synthesis of Esters from Aldehydes or Ketones and Carboxylic Acids

Org. Lett., 2018, 20, 24, 7856–7859 Impact factor:  6.005

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Hitchhiker’s Guide to Reductive Amination

Synth., 2019; 51, 13, 2667-2677, Impact Factor: 3.157

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Indenyl Rhodium Complexes with Arene Ligands: Synthesis and Application for Reductive Amination

Organometal., 2018, 37, 15, 2553–2562, Impact Factor:  3.876

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Carbon monoxide as a selective reducing agent in organic chemistry

Mend. Commun., 2018, 28 (2), 113-122, Impact Factor: 1.694

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Dichotomy of Atom-Economical Hydrogen-Free Reductive Amidation vs Exhaustive Reductive Amination

Org. Lett., 2017, 19, 20, 5657–5660, Impact Factor: 6.005

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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

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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

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Hydrogen-Free Reductive Amination Using Iron Pentacarbonyl as a Reducing Agent

Org. Biomol. Chem., 2017, 15, 10164–10166, Impact Factor: 3.412

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Cyclobutadiene Arene Complexes of Rhodium and Iridium

Organometal., 2016, 35, 17, 3025–3031, Impact Factor: 3.876

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Dichotomy of Reductive Addition of Amines to Cyclopropyl Ketones vs Pyrrolidine Synthesis

Org. Lett., 2016, 18, 22, 5968–5970, Impact Factor: 6.005

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The synthesis of sterically hindered amines by a direct reductive amination of ketones

Chem. Commun., 2016, 52, 1397-1400, Impact Factor: 5.996

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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

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Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source

Org. Lett., 2015, 17, 2, 173–175, Impact Factor:  6.005

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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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Reductive Amination without an External Hydrogen Source

Angew. Chem. Int. Ed., 2014, 53, 5199-5201, Impact Factor: 15.336

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Atom- and Step-Economical Preparation of Reduced Knoevenagel Adducts Using CO as a Deoxygenative Agent

Org. Lett., 2014, 16, 19, 5068–5071, Impact Factor: 6.005

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