Старосотников Алексей Михайлович

Публикации в базе данных Math-Net.Ru

1. C–H functionalization of highly electrophilic azolopyridines as a way to donor–acceptor conjugated indoles
   
   Mendeleev Commun., 35:6 (2025),  648–650
2. Прогресс в химии азот-, кислород- и серасодержащих гетероциклических систем
   
   Усп. хим., 89:1 (2020),  55–124
3. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds
   
   Mendeleev Commun., 28:6 (2018),  638–640
4. Synthesis of nitro pyrido- and dipyrido[1,4]oxazines
   
   Mendeleev Commun., 26:5 (2016),  383–385
5. Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan
   
   Mendeleev Commun., 26:3 (2016),  217–219
6. 5-Nitro-7,8-furoxanoquinoline: a new type of fused nitroarenes possessing Diels–Alder reactivity
   
   Mendeleev Commun., 24:4 (2014),  203–205
7. Synthesis of fused isoindoles via 1,3-dipolar cycloaddition of 1,3-oxazolium-5-olates (münchnones) with nitro benzazoles
   
   Mendeleev Commun., 22:1 (2012),  35–36
8. 4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide
   
   Mendeleev Commun., 20:6 (2010),  353–354
9. Superelectrophilic nature of 4,6-dinitrobenzo[c]isoxazole (4,6-dinitroanthranil) in [4+2]-cycloaddition reactions and σ^H-complex formation
   
   Mendeleev Commun., 20:3 (2010),  165–166
10. Synthesis of polycyclic indole derivatives from 2,4,6-trinitrotoluene
    
    Mendeleev Commun., 19:1 (2009),  47–48
11. Synthesis of 3-substituted 1,5-dinitro-3-azabicyclo-[3.3.1]nonanes containing a pyrazole fragment
    
    Mendeleev Commun., 18:4 (2008),  213–214
12. Synthesis of 14π-electron peri-annelated tricyclic heteroaromatic systems based on 2,4,6-trinitrotoluene
    
    Mendeleev Commun., 12:5 (2002),  200–202
13. Synthesis and reactions of 1-aryl-3-formyl-4,6-dinitro-1H-indazoles
    
    Mendeleev Commun., 12:5 (2002),  198–200
14. Synthesis and transformations of picrylacetaldehyde
    
    Mendeleev Commun., 10:4 (2000),  140–141