Далингер Игорь Львович

Публикации в базе данных Math-Net.Ru

1. Nucleophilic substitution in azasydnone-modified dinitroanisoles
   
   Mendeleev Commun., 35:3 (2025),  271–273
2. Unusual formation of 4-diazo-3-nitriminopyrazoles upon acid nitration of pyrazolo[3,4-d][1,2,3]triazoles
   
   Mendeleev Commun., 35:3 (2025),  249–251
3. Polynitropyrazole derivatives of pentanitroisowurtzitane
   
   Mendeleev Commun., 34:5 (2024),  703–705
4. Ethyl butyrates bearing nitro and difluoroamino groups
   
   Mendeleev Commun., 33:6 (2023),  841–843
5. New heterocyclic furazano[3,4-d ][1,2,3]triazine system as a platform for energetic compound engineering
   
   Mendeleev Commun., 32:6 (2022),  717–719
6. Прогресс в химии азот-, кислород- и серасодержащих гетероциклических систем
   
   Усп. хим., 89:1 (2020),  55–124
7. Нитросоединения — структурная основа перспективных энергоемких материалов и многоцелевые реагенты для органического синтеза
   
   Усп. хим., 89:1 (2020),  1–54
8. A new general synthesis of functionally substituted pyrazolo[1,5-a]pyrimidines
   
   Mendeleev Commun., 29:4 (2019),  429–431
9. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds
   
   Mendeleev Commun., 28:6 (2018),  638–640
10. Recent advances in synthesis of organic nitrogen–oxygen systems for medicine and materials science
    
    Mendeleev Commun., 27:6 (2017),  535–546
11. Acetonylation of 5(3)-(1H-tetrazol-1-yl)-3(5)-nitro-1H-pyrazole
    
    Mendeleev Commun., 27:5 (2017),  462–463
12. Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan
    
    Mendeleev Commun., 26:3 (2016),  217–219
13. Novel highly energetic pyrazoles: N-fluorodinitromethyl and N-[(difluoroamino)dinitromethyl] derivatives
    
    Mendeleev Commun., 25:6 (2015),  429–431
14. Hydrogen halides as nucleophilic agents for 3,4,5-trinitro-1H-pyrazoles
    
    Mendeleev Commun., 22:1 (2012),  43–44
15. Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole
    
    Mendeleev Commun., 21:3 (2011),  149–150
16. N-Fluoro derivatives of nitrated pyrazole-containing fused heterocycles
    
    Mendeleev Commun., 21:1 (2011),  48–49
17. Synthesis of 4-(N-azolyl)-3,5-dinitropyrazoles
    
    Mendeleev Commun., 20:6 (2010),  355–356
18. The specific reactivity of 3,4,5-trinitro-1H-pyrazole
    
    Mendeleev Commun., 20:5 (2010),  253–254
19. Динитропиразолы
    
    Усп. хим., 78:7 (2009),  643–682
20. Synthesis and transformations of picrylacetaldehyde
    
    Mendeleev Commun., 10:4 (2000),  140–141
21. Regioselectivity of the substitution for the nitro group in 2,4,6-trinitrobenzonitrile under the action of thiols. The synthesis of 4,6-dinitro derivatives of benzoannelated sulfur-containing heterocycles
    
    Mendeleev Commun., 10:2 (2000),  72–73
22. Synthesis of 4-diazo-3,5-dinitropyrazole and characteristic features of its behaviour towards nucleophiles
    
    Mendeleev Commun., 7:2 (1997),  58–59
23. Synthesis of N-hydroxypyrazoles with electron-accepting substituents in the ring
    
    Mendeleev Commun., 6:4 (1996),  139–140
24. N-(Difluoroamino)azoles – a new class of N-substituted azoles
    
    Mendeleev Commun., 6:1 (1996),  13–15
25. N-Nitropyrazoles, a new source of nitrogen monoxide
    
    Mendeleev Commun., 6:1 (1996),  11–12
26. N-Amination of Pyrazoles: a General Approach
    
    Mendeleev Commun., 3:3 (1993),  111
27. ¹⁵N and ¹⁷O NMR Spectral Parameters of M-Nitropyrazoles
    
    Mendeleev Commun., 3:3 (1993),  109–110
28. Interaction of NH-Azoles with O-Fluorosulfonyl-N,N-difluorohydroxylamine
    
    Mendeleev Commun., 3:1 (1993),  14–15