Kravchenko Angelina Nikolaevna

Publications in Math-Net.Ru

1. Highly regioselective synthesis and structure of 1-substituted 3a,6,6a-triphenylglycolurils
   
   Mendeleev Commun., 35:1 (2025),  27–30
2. Novel synthesis of 1,6- and 1,4-dialkyl glycolurils and their supramolecular organization
   
   Mendeleev Commun., 34:6 (2024),  871–874
3. Synthesis of new functionalized thiazolidin-4-ones by the condensation of thioureas with dialkyl acetylenedicarboxylates
   
   Mendeleev Commun., 34:4 (2024),  563–565
4. Synthesis of new heterylmethylidene derivatives of isomeric imidazo[4,5-e]thiazolo-fused [1,2,4]triazines
   
   Mendeleev Commun., 34:4 (2024),  558–560
5. An efficient synthesis of substituted 4,5-dihydroxyimidazolidin-2-ones by oxidation of imidazolin-2-ones with HNO₃
   
   Mendeleev Commun., 34:1 (2024),  116–118
6. Synthesis of trialkyl semithioglycolurils from alkylthiourea-glyoxal cyclic adducts and dialkylureas
   
   Mendeleev Commun., 32:6 (2022),  771–773
7. Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers
   
   Mendeleev Commun., 32:5 (2022),  678–679
8. Synthesis and crystal structures of novel glycoluril carboxylic acids conglomerates
   
   Mendeleev Commun., 32:4 (2022),  537–539
9. New aspects of reactions of methyl (thio)ureas with benzil
   
   Mendeleev Commun., 31:5 (2021),  673–676
10. New cage-fused polyaza polycyclic systems based on thioglycolurils and alkanediamines
    
    Mendeleev Commun., 30:4 (2020),  479–481
11. Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems
    
    Usp. Khim., 89:1 (2020),  55–124
12. Highly selective synthesis of tricyclic compounds from semithioglycoluril, formaldehyde and amines
    
    Mendeleev Commun., 29:3 (2019),  323–325
13. A first synthesis of 8- and 8,10-substituted barbiturils and their thio analogues
    
    Mendeleev Commun., 29:1 (2019),  94–95
14. Preparative synthesis and pharmacological activity of Albicar racemate and enantiomers
    
    Mendeleev Commun., 28:3 (2018),  317–319
15. Synthesis of glycolurils and their analogues
    
    Usp. Khim., 87:1 (2018),  89–108
16. Efficient synthesis of N,N’-methylenebisglycolurils
    
    Mendeleev Commun., 26:2 (2016),  136–138
17. Unexpected formation of 6-[benzofuran-3(2H)-ylidene]-3,3a,9,9a-tetra-hydroimidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazine-2,7-dione derivative
    
    Mendeleev Commun., 25:6 (2015),  476–478
18. Self-organization and chirality in the high dilution solutions of glycoluril enantiomers with (R)- and (S)-methionine moieties
    
    Mendeleev Commun., 25:1 (2015),  72–74
19. Regioselective synthesis of 2,8-disubstituted 1,5-diphenylglycolurils
    
    Mendeleev Commun., 24:3 (2014),  173–175
20. Cascade synthesis of the first imidazo[4,5-e]-thiazolo[2,3-c][1,2,4]triazine derivative
    
    Mendeleev Commun., 24:2 (2014),  119–121
21. Synthesis of new ring-fused thiocarbamates by condensation of 2-thioxo-and 2-oxo-1,3-dialkyl-4,5-dihydroxy-4,5-diphenylimidazolidines with KSCN
    
    Mendeleev Commun., 24:2 (2014),  105–107
22. Unexpected formation of 4-alkyl-5-(4-alkylthiosemicarbazido)-4,5-dihydro-1,2,4-triazine-3(2H)-thiones from 1,3-dialkyl-4,5-bis-(4-alkylthiosemicarbazido)imidazolidin-2-ones in acidic medium
    
    Mendeleev Commun., 24:1 (2014),  42–44
23. Correlations between the self-organization, physicochemical properties and biological activity of Mebicar in dilute aqueous solutions
    
    Mendeleev Commun., 23:5 (2013),  262–264
24. Target synthesis of bioactive thioglycolurils, based on QSAR predictions
    
    Mendeleev Commun., 23:4 (2013),  202–203
25. Synthesis of 2,4,6-trialkyl-8-(2,3-epoxypropyl)glycolurils
    
    Mendeleev Commun., 23:2 (2013),  104–105
26. HNO₂-Assisted Triazine Cycle Contraction in 3-oxo-,3-thioxo- and 3-imino-5,7-dimethyl-4a,7a-diphenyl-perhydroimidazo[4,5-e][1,2,4]triazin-6-ones
    
    Mendeleev Commun., 22:6 (2012),  299–301
27. [3 + 2]-Cycloaddition of azomethine ylide at 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones
    
    Mendeleev Commun., 22:2 (2012),  90–91
28. Thiosemicarbazides in the synthesis of five- and six-membered heterocyclic compounds
    
    Usp. Khim., 81:6 (2012),  494–523
29. Reaction of 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo-[4,5-e]-1,3-thiazolo[3,2-b]-1,2,4-triazine-2,7(1H,6H)-dione with isatins
    
    Mendeleev Commun., 20:5 (2010),  288–290
30. Cyclization of 1,3-dialkyl-4,5-bis(1-thiosemicarbazido)-imidazolidin-2-ones(thiones) with aromatic aldehydes
    
    Mendeleev Commun., 20:5 (2010),  285–287
31. Condensation of 5,7-dimethyl-4a,7a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-one with halogenoacetic acids
    
    Mendeleev Commun., 20:1 (2010),  47–49
32. Syntheses of imidazo[4,5-e]-1,2,4-triazines via the reaction of 1,3-dimethyl-4,5-dihydroxy-4,5-diphenylimidazolidin-2-one with aminoguanidine and semicarbazide
    
    Mendeleev Commun., 19:5 (2009),  279–280
33. Co-crystals in the series of 4,5-dihydroxy- 4,5-diphenylimidazolidine-2-thiones
    
    Mendeleev Commun., 19:4 (2009),  211–213
34. New generation of enantiomerically pure N-α-carboxyalkylglycolurils
    
    Mendeleev Commun., 18:2 (2008),  96–98
35. A new approach to the synthesis of 1,3-dimethyl-4,5-disubstituted imidazolidin-2-ones
    
    Mendeleev Commun., 18:1 (2008),  45–47
36. Synthesis of enantiomerically pure fused polyheterocyclic glycolurils based on (S)- α-amino acids
    
    Mendeleev Commun., 17:6 (2007),  321–322
37. The first conglomerate in the series of 2,4,6,8,10-pentaazatricyclo[5.3.1.0^3.11]undecane-1,5-diones
    
    Mendeleev Commun., 17:2 (2007),  85–87
38. The first synthesis of assemblies of imidazolidine rings by α-ureidoalkylation of imidazolidin-2-one with 4,5-dihydroxyimidazolidin-2-ones
    
    Mendeleev Commun., 16:2 (2006),  80–82
39. Chemistry of ureido carboxylic and ureylene dicarboxylic acids
    
    Usp. Khim., 75:3 (2006),  217–233
40. Synthesis of (S)-N-hydantoinoalkylglycoluriles by one-pot double cyclisation of chiral α,ω-diureido acids under the action of 4,5-dihydroxyimidazolidin-2-ones
    
    Mendeleev Commun., 15:2 (2005),  67–69
41. Synthesis of 1S,5R- and 1R,5S-glycoluriles by diastereospecific α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one
    
    Mendeleev Commun., 14:6 (2004),  253–255
42. New conglomerate in the series of glycoluriles
    
    Mendeleev Commun., 14:3 (2004),  105–107
43. Highly diastereoselective synthesis of 2-monosubstituted 1R,5S(1S,5R)-glycoluriles on the basis of S- and R-N-carbamoyl-α-amino acids
    
    Mendeleev Commun., 13:6 (2003),  269–271
44. A new simple approach to the preparation of imidazo [4,5-e]-1,2,4-triazine derivatives
    
    Mendeleev Commun., 13:4 (2003),  190–192
45. Spontaneous resolution in the imidazolidin-2-one series
    
    Mendeleev Commun., 13:3 (2003),  114–116
46. Chiral drugs via the spontaneous resolution
    
    Mendeleev Commun., 12:1 (2002),  6–8
47. 3,3’-Bi(6,8-dialkyl-2,4-dioxa-7-thia-6,8-diazabicyclo[3.3.0]octane 7,7-dioxides) as new heterocyclic system derivatives
    
    Mendeleev Commun., 11:4 (2001),  138–140
48. Crystal properties of N-alkyl-substituted glycolurils as the precursors of chiral drugs
    
    Mendeleev Commun., 11:4 (2001),  134–136
49. Reaction of 1,3-diethyl-4,5-dihydroxyimidazolidin-2-one with 1,3-dimethylsulfamide at a high pressure
    
    Mendeleev Commun., 11:3 (2001),  107–108
50. New functional glycoluril derivatives
    
    Mendeleev Commun., 11:1 (2001),  32–33
51. Unusual reactions of 6,8-dialkyl-3-thia-2,4,6,8-tetraazabicyclo[3.3.0]octan-7-one 3,3-dioxides under conditions of acid hydrolysis and acetylation
    
    Mendeleev Commun., 10:6 (2000),  232–233
52. Synthesis of new heterocyclic sulfamides
    
    Mendeleev Commun., 10:1 (2000),  28–29
53. New condensation methods in the synthesis of bicyclic bisureas
    
    Mendeleev Commun., 10:1 (2000),  27–28
54. Sulfamides in the synthesis of heterocyclic compounds
    
    Usp. Khim., 69:3 (2000),  239–248
55. Chiral glycouril, 2,6-diethyl-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione: spontaneous resolution, reactivity and absolute configuration
    
    Mendeleev Commun., 8:6 (1998),  231–233
56. New products from the reactions of 4,5-dihydroxyimidazolidin-2-ones with sulfonamides
    
    Mendeleev Commun., 6:2 (1996),  68–69
57. The Surface Molecular Potential Method for Calculating the Structure–Activity Relationship for Psychotropic Compounds
    
    Mendeleev Commun., 5:2 (1995),  49–51