Собенина Любовь Николаевна

Публикации в базе данных Math-Net.Ru

1. One-pot synthesis of functionalized dihydroindolizinones from pyrrolylpropynoates and diethyl aminomalonate
   
   Mendeleev Commun., 35:1 (2025),  99–101
2. One-pot synthesis of pyrrolooxazoles from pyrrolyl acetylenic ketones and natural aldehydes
   
   Mendeleev Commun., 35:1 (2025),  14–17
3. A facile synthesis of 2-ethynylpyrroles by Bu^tOK-assisted room temperature deprotection of 2-(acylethynyl)pyrroles
   
   Mendeleev Commun., 33:4 (2023),  458–460
4. Замещенные пирролы на основе кетонов: перспективы использования и достижения в синтезе
   
   Усп. хим., 92:9 (2023),  1–30
5. Acyl-tetrahydroindolyl-capped 1,3-diynes in oxidative [4 + 2]-cycloaddition with benzylamine: a one-pot access to 2-acyl-6-phenyl-5-tetrahydroindolylpyridines
   
   Mendeleev Commun., 32:6 (2022),  729–731
6. Conjugated pyrrole/aminoenone and pyrrole/aminoacrylonitrile ensembles: new motives in heterocyclic chemistry
   
   Mendeleev Commun., 31:5 (2021),  573–583
7. Acetylene based short route from 2,2,6,6-tetramethylpiperidin-4-one oxime to 2-(pyrazol-5-yl)-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines
   
   Mendeleev Commun., 29:6 (2019),  658–660
8. Copper(I) halide-promoted formation of 3-acyl-5-halopyridine moiety from NH-2-(2-acylethynyl)pyrroles and propargylamine
   
   Mendeleev Commun., 29:3 (2019),  252–253
9. 1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
   
   Mendeleev Commun., 29:1 (2019),  53–54
10. Перспективные точки роста и вызовы фторорганической химии
    
    Усп. хим., 88:5 (2019),  425–569
11. Reaction of 1-(het)aryl-3-bromoprop-2-ynones with furans in solid metal oxides or salts: cross-coupling or cycloaddition?
    
    Mendeleev Commun., 28:1 (2018),  20–21
12. Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    
    Mendeleev Commun., 27:4 (2017),  344–345
13. Aluminium oxide-mediated cross-coupling of pyrroles with 1-bromo-2-(trifluoroacetyl)acetylene: a quantum-chemical insight
    
    Mendeleev Commun., 26:6 (2016),  480–482
14. C-Этинилпирролы: синтез и реакционная способность
    
    Усп. хим., 83:6 (2014),  475–501
15. 2-(2-Benzoylethynyl)-5-phenylpyrrole: fixation of cis- and trans-rotamers in a crystal state
    
    Mendeleev Commun., 15:6 (2005),  229–232
16. Синтез C-винилпирролов
    
    Усп. хим., 71:7 (2002),  641–671
17. An example of the facile C-vinylation of pyrroles
    
    Mendeleev Commun., 8:3 (1998),  119–120
18. Synthesis of 1H- and 1-vinyl-2-pyridylpyrroles by the Trofimov reaction
    
    Mendeleev Commun., 7:4 (1997),  162–163
19. Синтез пирролов из алифатических соединений
    
    Усп. хим., 58:2 (1989),  275–302