Moscow, Russia, 119334

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Publications

Reductive Amination without an External Hydrogen Source

Angew. Chemie Int. Ed., 2014, 53, 5199-5201, Impact Factor: 12.102


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

Org. Lett., 2014, 16, 19, 5068–5071, Impact Factor: 6.579

Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source

Org. Lett., 2015, 17, 2, 173–175, Impact Factor: 6.579

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

Cyclobutadiene Arene Complexes of Rhodium and Iridium

Organometallics, 2016, 35, 17, 3025–3031, Impact Factor: 3.862

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

Org. Lett., 2016, 18, 22, 5968–5970, Impact Factor: 6.579

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

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

Org. Lett., 2017, 19, 20, 5657–5660, Impact Factor: 6.492

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

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