Konstantinova Lidia Sergeevna

Publications in Math-Net.Ru

1. Chalcogen exchange in chalcogen–nitrogen π-heterocycles
   
   Mendeleev Commun., 31:4 (2021),  433–441
2. Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems
   
   Usp. Khim., 89:1 (2020),  55–124
3. A short and efficient synthesis of 5,5’ -bi-1,2,3-dithiazoles
   
   Mendeleev Commun., 25:6 (2015),  427–428
4. [1,4]Dithiino[2,3-c:5,6-c’ ]bis[1,2,5]oxadiazole di-N-oxide: synthesis and oxidation to mono- and bis-S-oxides
   
   Mendeleev Commun., 25:5 (2015),  339–340
5. Sulfur monochloride in organic synthesis
   
   Usp. Khim., 83:3 (2014),  225–250
6. 4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide
   
   Mendeleev Commun., 20:6 (2010),  353–354
7. [(4-Sulfanylidene-4H-1λ⁴,3,2-dithiazol-5-yl)sulfanyl]formic acid derivatives: synthesis from 5-oxo[1,3]dithiolo[4,5-d][1,3,2]dithiazol-1-ium chloride and structural characterization
   
   Mendeleev Commun., 20:5 (2010),  279–281
8. Unexpected formation of 5,5-diethoxy-5H-1,2,3-dithiazoles from 5H-1,2,3-dithiazole-5-thiones
   
   Mendeleev Commun., 20:4 (2010),  212–214
9. Identification of the [1,3]dithiolo[4,5-d]dithiazolyl radical
   
   Mendeleev Commun., 20:2 (2010),  80–82
10. Synthesis of 1,2,5-thiadiazole-3(2H)-thiones and 1,2,5-thiadiazol-3(2H)-ones from 1,2,3-dithiazoles
    
    Mendeleev Commun., 19:2 (2009),  84–86
11. Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects
    
    Mendeleev Commun., 19:2 (2009),  55–61
12. Synthesis and properties of 1,2,3-dithiazoles
    
    Usp. Khim., 77:6 (2008),  551–577
13. 1,2,3,4,5-Pentathiepines and 1,2,3,4,5-pentathiepanes
    
    Usp. Khim., 76:3 (2007),  219–236
14. Thienopentathiepins and pentathiepinofuran
    
    Mendeleev Commun., 16:6 (2006),  289–290
15. Regioselective synthesis of pentathiepino-fused pyrroles and indoles
    
    Mendeleev Commun., 14:3 (2004),  91–92
16. Direct conversion of N-ethylamines into functionalised amides by S₂Cl₂
    
    Mendeleev Commun., 11:5 (2001),  167–168
17. New reactions of Hünig's base with S₂Cl₂: formation of monocyclic 1,2-dithioles
    
    Mendeleev Commun., 11:5 (2001),  165–166
18. 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
19. Hypohalites as reagents for the macrocyclization of diamines of the furazan series
    
    Mendeleev Commun., 6:5 (1996),  193–195
20. Polydiazenofurazans: novel macrocyclic systems
    
    Mendeleev Commun., 6:2 (1996),  66–67
21. New Macrocyclic Systems – Tetrafurazano[3,4-c:3,4-e:3,4-i:3,4-k]-1,2,7,8-tetraazacyclododeca-1,3,5,7,9,11-hexane and Hexafurazano-[3,4-c:3,4-e:3,4-i:3,4-k:3,4-o:3,4-r]-1,2,7,8,13,14-hexaazacyclooctadeca-1,3,5,7,9,11,13,15,17-nonane by Oxidative Macrocyclization of Diaminodifurazanyl
    
    Mendeleev Commun., 4:3 (1994),  102