Publications
Reductive Amidation without an External Hydrogen Source Using Rhodium on Carbon Matrix as a Catalyst
ChemCatChem, 2020, 12, 1, 112-117, Impact Factor: 4.853
A Dual Threat: Redox‐Activity and Electronic Structures of Well‐Defined Donor–Acceptor Fulleretic Covalent‐Organic Materials
Angew. Chemie, 2020, 59, 15, 6000-6006, Impact Factor: 12.959
Rhodium‐Catalyzed Reductive Esterification Using Carbon Monoxide as a Reducing Agent
EurJOC, 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: 2.304
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
Variability of Rhodium(III)-Catalyzed Reactions of Aromatic Oximes with Alkenes
Synlett, 2020; 31, 11, 1117-1120, Impact Factor: 2.025
Alkyl formates as reagents for reductive amination of carbonyl compounds
Mendeleev Commun., 2020, 30, 1, 112-113, Impact Factor: 1.694
Direct Reductive Amination of Camphor Using Iron Pentacarbonyl as Stoichiometric Reducing Agent: Features and Limitations
EurJOC, 2020; 38, 6289-6294, Impact Factor: 2.889
Fluorene Complexes of Group 9 Metals: Fluorene Effect and Application for Reductive Amination
Organometallics, 2019, 38, 16, 3151–3158, Impact Factor: 3.804
One‐Pot Synthesis of Symmetrical Tertiary and Secondary Amines from Carbonyl Compounds, Ammonium Carbonate and Carbon Monoxide as a Reductant
EurJOC, 2019; 38, 6557-6560, Impact Factor: 2.889
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: 3.412
Synthesis of Nitriles from Aldehydes with Elongation of the Molecule with Two Carbon Atoms
EurJOC, 2019, 1, 32-35, Impact factor: 2.889
Indenyl Rhodium Complexes with Arene Ligands: Synthesis and Application for Reductive Amination
Organometallics, 2018, 37, 15, 2553–2562, Impact Factor: 3.862
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: 6.091
Dichotomy of Atom-Economical Hydrogen-Free Reductive Amidation vs Exhaustive Reductive Amination
Org. Lett., 2017, 19, 20, 5657–5660, Impact Factor: 6.091
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: 12.102
Synthesis of N,N′-Dialkylated Cyclohexane-1,2-diamines and Their Application as Asymmetric Ligands and Organocatalysts for the Synthesis of Alcohols
Synlett , 2017, 28, 05, 615-619, Impact Factor: 2.151
Hydrogen-Free Reductive Amination Using Iron Pentacarbonyl as a Reducing Agent
Org. Biomol. Chem., 2017, 15, 10164–10166, Impact Factor: 3.423
Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source
Org. Lett., 2015, 17, 2, 173–175, Impact Factor: 6.091
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: 4.803
The synthesis of sterically hindered amines by a direct reductive amination of ketones
Chem. Commun., 2016, 52, 1397-1400, Impact Factor: 6.319
Cyclobutadiene Metal Complexes: A New Class of Highly Selective Catalysts. An Application to Direct Reductive Amination
ACS Catal., 2016, 6, 3, 2043–2046, Impact Factor: 10.614
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