Лебедев Олег Васильевич

Публикации в базе данных Math-Net.Ru

1. A new approach to the synthesis of 1,3-dimethyl-4,5-disubstituted imidazolidin-2-ones
   
   Mendeleev Commun., 18:1 (2008),  45–47
2. 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
3. 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
4. New conglomerate in the series of glycoluriles
   
   Mendeleev Commun., 14:3 (2004),  105–107
5. 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
6. A new simple approach to the preparation of imidazo [4,5-e]-1,2,4-triazine derivatives
   
   Mendeleev Commun., 13:4 (2003),  190–192
7. Spontaneous resolution in the imidazolidin-2-one series
   
   Mendeleev Commun., 13:3 (2003),  114–116
8. Chiral drugs via the spontaneous resolution
   
   Mendeleev Commun., 12:1 (2002),  6–8
9. 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
10. Crystal properties of N-alkyl-substituted glycolurils as the precursors of chiral drugs
    
    Mendeleev Commun., 11:4 (2001),  134–136
11. 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
12. New functional glycoluril derivatives
    
    Mendeleev Commun., 11:1 (2001),  32–33
13. Synthesis of new heterocyclic sulfamides
    
    Mendeleev Commun., 10:1 (2000),  28–29
14. New condensation methods in the synthesis of bicyclic bisureas
    
    Mendeleev Commun., 10:1 (2000),  27–28
15. Сульфамиды в синтезе гетероциклических соединений
    
    Усп. хим., 69:3 (2000),  239–248
16. 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
17. First representatives of macrocyclic poly(diazene oxide furazans): 3,4:7,8:11,12:15,16-tetrafurazano-1,2,5,6,9,10,13,14-octaazacyclohexadeca-1,3,5,7,9,11,13,15-octaene 1,9- and 1,10-dioxides; 1,5,9,13-tetraoxide and its crystal structure
    
    Mendeleev Commun., 7:1 (1997),  5–7
18. Hypohalites as reagents for the macrocyclization of diamines of the furazan series
    
    Mendeleev Commun., 6:5 (1996),  193–195
19. New products from the reactions of 4,5-dihydroxyimidazolidin-2-ones with sulfonamides
    
    Mendeleev Commun., 6:2 (1996),  68–69
20. Polydiazenofurazans: novel macrocyclic systems
    
    Mendeleev Commun., 6:2 (1996),  66–67
21. The Surface Molecular Potential Method for Calculating the Structure–Activity Relationship for Psychotropic Compounds
    
    Mendeleev Commun., 5:2 (1995),  49–51