Пожарский Александр Федорович

Публикации в базе данных Math-Net.Ru

1. Why naturally occurring quinone redox systems lack amino groups: consideration using 1,4-naphthoquinone derivatives
   
   Mendeleev Commun., 34:2 (2024),  246–250
2. Успехи в химии гетероциклических соединений в 21 веке
   
   Усп. хим., 93:7 (2024),  1–366
3. α-Amino acid-assisted autoxidation of naphthalene proton sponge affording 1,4-naphthoquinone nitrogen derivatives
   
   Mendeleev Commun., 33:2 (2023),  197–200
4. Modelling biologically important NH$\cdots\pi$ interactions
   
   Усп. хим., 91:7 (2022),  1–38
5. Perimidines: a unique $\pi$-amphoteric heteroaromatic system
   
   Усп. хим., 89:11 (2020),  1204–1260
6. Бензо[g]индолы
   
   Усп. хим., 86:7 (2017),  589–624
7. Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives
   
   Mendeleev Commun., 25:3 (2015),  182–184
8. Proton Sponges and Hydrogen Transfer Phenomena
   
   Mendeleev Commun., 22:3 (2012),  117–124
9. Синтез гетероконденсированных птеридинов
   
   Усп. хим., 80:6 (2011),  523–557
10. tert-Amino effect in naphthalene proton sponges: a novel approach to benzo[h]quinoline and quino[7,8:7’,8’]quinoline derivatives
    
    Mendeleev Commun., 20:1 (2010),  36–38
11. Absolute configuration of a chiral proton sponge
    
    Mendeleev Commun., 18:2 (2008),  86–87
12. Spontaneous resolution of a chiral proton sponge
    
    Mendeleev Commun., 17:4 (2007),  214–215
13. Rearrangement of carbocations derived from 1,8-bis(dimethylamino)naphthyl-2-methanols into 4-R-1,1,3-trimethyl-2,3-dihydroperimidinium salts
    
    Mendeleev Commun., 16:6 (2006),  313–316
14. Литий- и магнийорганические соединения нафталинового ряда в органическом синтезе
    
    Усп. хим., 75:8 (2006),  791–819
15. Hexa- and heptasubstitution in the interaction of octafluoronaphthalene with lithium dialkylamides: a new approach to the naphthalene ‘proton sponges’
    
    Mendeleev Commun., 14:1 (2004),  14–16
16. Monohydrazine analogues of naphthalene and acenaphthene ‘proton sponges’
    
    Mendeleev Commun., 13:4 (2003),  180–182
17. Нафтальдегиды
    
    Усп. хим., 72:5 (2003),  498–523
18. 6,8-Dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-dione: a novel approach to imidazoline (imidazole) ring annulation based on the SNH methodology
    
    Mendeleev Commun., 12:4 (2002),  157–159
19. 2-Trifluoromethylperimidines with electron-withdrawing groups at the 6(7)-position: a case of extremely hindered annular prototropy
    
    Mendeleev Commun., 10:5 (2000),  178–180
20. Reaction of 6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-dione with α,ω-diamines as the first example of tandem nucleophilic substitution in neutral azines
    
    Mendeleev Commun., 10:4 (2000),  150–151
21. Нафталиновые протонные губки
    
    Усп. хим., 67:1 (1998),  3–27
22. Formation of 3-Amino-1,2,4-triazines by Thermolysis of Condensed N-Amino-α-Azidoimidazoles
    
    Mendeleev Commun., 2:1 (1992),  33–35
23. Different Behaviour of Fervenulin 4-Oxide and 1,3-Dimethyllumazine 5-Oxide towards Nucleophiles
    
    Mendeleev Commun., 1:2 (1991),  46–47
24. Unexpected Formation of Diels–Alder Spiro Adducts from 4-Hydroxymethyl Derivatives of ‘Proton Sponge’
    
    Mendeleev Commun., 1:1 (1991),  10–12
25. Перимидины
    
    Усп. хим., 50:9 (1981),  1559–1600
26. Успехи в изучении реакции Чичибабина
    
    Усп. хим., 47:11 (1978),  1933–1969
27. Кислотные свойства аминогруппы
    
    Усп. хим., 42:1 (1973),  65–101
28. Успехи химии имидазола
    
    Усп. хим., 35:2 (1966),  261–302