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Красавин Михаил Юрьевич

Публикации в базе данных Math-Net.Ru

  1. Convenient, DBU-promoted anti-Markovnikov hydration of 2-methyl-1-(3-arylprop-2-yn-1-yl)-1H-imidazoles in wet NMP

    Mendeleev Commun., 33:4 (2023),  455–457
  2. A new way of synthesizing heterocyclic primary sulfonamide probes for carbonic anhydrase

    Mendeleev Commun., 33:3 (2023),  325–327
  3. Spirocyclic azetidines for drug discovery: Novel Boc-protected 7'H-spiro[azetidine-3,5'-furo[3,4-d ]pyrimidines]

    Mendeleev Commun., 33:3 (2023),  323–324
  4. Synthesis of 1-oxa-9-azaspiro[5.5]undecane-9-sulfonamides bearing a diverse molecular periphery and a rare zinc-binding group for carbonic anhydrase interrogation

    Mendeleev Commun., 33:2 (2023),  191–193
  5. Urea derivatives of spirocyclic piperidines endowed with antibacterial activity

    Mendeleev Commun., 33:1 (2023),  109–111
  6. Synthesis of novel glutarimide derivatives via the Michael addition of (hetero)aromatic thiols: pronounced effect of sulfur oxidation on cytotoxicity towards multiple myeloma cell lines

    Mendeleev Commun., 33:1 (2023),  67–69
  7. Diazo chemistry in the access to novel fatty acids linked to spiro-fused oxetane-pyrazolone scaffold

    Mendeleev Commun., 33:1 (2023),  21–23
  8. Synthesis of novel glutarimide derivatives via the Ugi multicomponent reaction: affinity towards the E3 ubiquitin ligase substrate receptor Cereblon

    Mendeleev Commun., 32:6 (2022),  747–749
  9. Synthesis of a library of 2-aryl-2H-tetrazole-5-carboxamides for photoaffinity labeling of aminergic G-protein coupled receptors

    Mendeleev Commun., 32:5 (2022),  604–605
  10. Hetaryl- and heteroarylvinyl-substituted nitrofurans identified as non-cytotoxic selective antitubercular agents

    Mendeleev Commun., 32:4 (2022),  452–453
  11. Synthetic approaches to constructing proteolysis targeting chimeras (PROTACs)

    Mendeleev Commun., 32:4 (2022),  419–432
  12. Novel chromeno[2,3-c]pyrroles synthesized via intramolecular rhodium(ii) carbene trapping

    Mendeleev Commun., 32:3 (2022),  382–383
  13. (E)-3-Arylidene-4-diazopyrrolidine-2,5-diones conveniently elaborated into cytotoxic compounds bearing primary sulfonamide and Michael acceptor moieties

    Mendeleev Commun., 32:2 (2022),  176–177
  14. Novel medium-sized di(het)areno-fused 1,4,7-(oxa)thiadiazecines as probes for aminergic receptors

    Mendeleev Commun., 31:4 (2021),  501–503
  15. Rare cis-configured 2,4-disubstituted 1-alkylpiperidines: synthesized and tested against trace-amine-associated receptor 1 (TAAR1)

    Mendeleev Commun., 31:4 (2021),  488–489
  16. Convenient preparation of (E)-3-arylidene-4-diazopyrrolidine-2,5-diones in array format

    Mendeleev Commun., 31:1 (2021),  36–38
  17. The Castagnoli–Cushman reaction of bicyclic pyrrole dicarboxylic anhydrides bearing electron-withdrawing substituents

    Mendeleev Commun., 30:4 (2020),  496–497
  18. Taking diazo transfer to water: α-diazo carbonyl compounds from in situ generated mesyl azide

    Mendeleev Commun., 30:3 (2020),  372–373
  19. One-pot preparation of methyl 2-diazo-3-oxopropionates comprising an aqueous ‘sulfonyl-azide-free’ (SAFE) diazo transfer step

    Mendeleev Commun., 30:3 (2020),  311–312
  20. Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction

    Mendeleev Commun., 29:3 (2019),  337–338
  21. 1,1′-Carbonyldiimidazole as a cyclodehydrating agent for the Castagnoli–Cushman reaction of dicarboxylic acids and imines

    Mendeleev Commun., 29:3 (2019),  292–293
  22. Microwave-promoted reaction of N-(alk-1-enyl)chloroacetamides with sodium azide unexpectedly yields 1H-imidazol-5(4H)-ones

    Mendeleev Commun., 27:1 (2017),  95–96
  23. Increased dipeptoid diversity resulting from post-condensational manipulation of the Ugi reaction products

    Mendeleev Commun., 22:1 (2012),  41–42
  24. Многокомпонентные реакции изоцианидов в синтезе гетероциклов

    Усп. хим., 79:9 (2010),  861–893


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