Reductive amination in the synthesis of pharmaceuticals OI Afanasyev, E Kuchuk, DL Usanov, D Chusov Chemical reviews 119 (23), 11857-11911, 2019 | 502 | 2019 |
Hitchhiker’s guide to reductive amination E Podyacheva, OI Afanasyev, AA Tsygankov, M Makarova, D Chusov Synthesis 51 (13), 2667-2677, 2019 | 90 | 2019 |
Cyclobutadiene metal complexes: a new class of highly selective catalysts. An application to direct reductive amination OI Afanasyev, AA Tsygankov, DL Usanov, DS Perekalin, NV Shvydkiy, ... ACS Catalysis 6 (3), 2043-2046, 2016 | 62 | 2016 |
Borrowing hydrogen amination reactions: A complex analysis of trends and correlations of the various reaction parameters E Podyacheva, OI Afanasyev, DV Vasilyev, D Chusov ACS Catalysis 12 (12), 7142-7198, 2022 | 49 | 2022 |
Reductive amination catalyzed by iridium complexes using carbon monoxide as a reducing agent AP Moskovets, DL Usanov, OI Afanasyev, VA Fastovskiy, AP Molotkov, ... Organic & Biomolecular Chemistry 15 (30), 6384-6387, 2017 | 41 | 2017 |
Dichotomy of reductive addition of amines to cyclopropyl ketones vs pyrrolidine synthesis OI Afanasyev, AA Tsygankov, DL Usanov, D Chusov Organic letters 18 (22), 5968-5970, 2016 | 30 | 2016 |
Redox Condensations of o-Nitrobenzaldehydes with Amines under Mild Conditions: Total Synthesis of the Vasicinone Family OI Afanasyev, E Podyacheva, A Rudenko, AA Tsygankov, M Makarova, ... The Journal of Organic Chemistry 85 (14), 9347-9360, 2020 | 29 | 2020 |
Hydrogen-free reductive amination using iron pentacarbonyl as a reducing agent OI Afanasyev, DL Usanov, D Chusov Organic & Biomolecular Chemistry 15 (48), 10164-10166, 2017 | 19 | 2017 |
Symmetrical tertiary amines: applications and synthetic approaches OI Afanasyev, EA Kuchuk, KM Muratov, GL Denisov, D Chusov European Journal of Organic Chemistry 2021 (4), 543-586, 2021 | 18 | 2021 |
Aldehydes as alkylating agents for ketones SA Runikhina, OI Afanasyev, K Biriukov, DS Perekalin, M Klussmann, ... Chemistry–A European Journal 25 (71), 16225-16229, 2019 | 18 | 2019 |
Reductive Amidation without an External Hydrogen Source Using Rhodium on Carbon Matrix as a Catalyst AA Tsygankov, M Makarova, OI Afanasyev, AS Kashin, AV Naumkin, ... ChemCatChem 12 (1), 112-117, 2020 | 14 | 2020 |
Synthesis of the cyclopentadienone rhodium complexes and investigation of their catalytic activity in the reductive amination of aldehydes in the presence of carbon monoxide RA Pototskiy, OI Afanasyev, YV Nelyubina, D Chusov, AR Kudinov, ... Journal of Organometallic Chemistry 835, 6-11, 2017 | 14 | 2017 |
Some Aspects of Reductive Amination in the Presence of Carbon Monoxide: Cyclopropyl Ketones as Bifunctional Electrophiles OI Afanasyev, AA Tsygankov, DL Usanov, DS Perekalin, AD Samoylova, ... Synthesis 49 (12), 2640, 2017 | 13 | 2017 |
Enhancing the efficiency of the ruthenium catalysts in the reductive amination without an external hydrogen source AR Fatkulin, OI Afanasyev, AA Tsygankov, D Chusov Journal of Catalysis 405, 404-409, 2022 | 12 | 2022 |
Borrowing hydrogen amination: Whether a catalyst is required? AS Kozlov, OI Afanasyev, D Chusov Journal of Catalysis 413, 1070-1076, 2022 | 11 | 2022 |
Syngas Instead of Hydrogen Gas as a Reducing Agent─ A Strategy To Improve the Selectivity and Efficiency of Organometallic Catalysts E Podyacheva, OI Afanasyev, VS Ostrovskii, D Chusov ACS catalysis 12 (9), 5145-5154, 2022 | 11 | 2022 |
Osmium catalysis in the reductive amination using carbon monoxide as a reducing agent MM Vinogradov, OI Afanasyev, YV Nelyubina, GL Denisov, DA Loginov, ... Molecular Catalysis 498, 111260, 2020 | 9 | 2020 |
Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power KO Biriukov, MM Vinogradov, OI Afanasyev, DV Vasilyev, AA Tsygankov, ... Catalysis Science & Technology 11 (14), 4922-4930, 2021 | 8 | 2021 |
Alkyl formates as reagents for reductive amination of carbonyl compounds OI Afanasyev, G Denisov, D Chusov, I Cherkashchenko, A Kuznetsov, ... Mendeleev Communications 30 (1), 112-113, 2020 | 8 | 2020 |
Direct reductive amination of camphor using iron pentacarbonyl as stoichiometric reducing agent: features and limitations OI Afanasyev, AR Fatkulin, PN Solyev, I Smirnov, A Amangeldyev, ... European Journal of Organic Chemistry 2020 (39), 6289-6294, 2020 | 7 | 2020 |