Kadorkina Gulnara K

Публикации в базе данных Math-Net.Ru

1. 1-Alkoxyamino-4-dimethylaminopyridinium salts: synthesis and structure^†
   
   Mendeleev Commun., 26:2 (2016),  169–171
2. Synthesis and structure of N-alkoxyhydrazines and N-alkoxy-N’,N’,N’-trialkylhydrazinium salts
   
   Mendeleev Commun., 23:5 (2013),  289–291
3. The enigma of a (±)-tartaric acid–urea cocrystal
   
   Mendeleev Commun., 19:1 (2009),  17–18
4. Absolute configuration of a chiral proton sponge
   
   Mendeleev Commun., 18:2 (2008),  86–87
5. Spontaneous resolution of a chiral proton sponge
   
   Mendeleev Commun., 17:4 (2007),  214–215
6. The first conglomerate in fluorinated asymmetric nitrogen compounds
   
   Mendeleev Commun., 16:3 (2006),  139–141
7. Stereochemistry of 1,2,4,5-tetraazanorbornanes and diaziridines: exciting history and news
   
   Mendeleev Commun., 14:6 (2004),  315–318
8. Stereochemisty of 3,3-disubstituted 2-methoxy-1,2-oxazolidines
   
   Mendeleev Commun., 14:6 (2004),  306–309
9. Spontaneous resolution in the imidazolidin-2-one series
   
   Mendeleev Commun., 13:3 (2003),  114–116
10. Asymmetric three-coordinated nitrogen compounds: spontaneous resolution and absolute asymmetric synthesis
    
    Mendeleev Commun., 13:3 (2003),  111–113
11. Pasteur-like resolution of quasi-racemates in solid and gas phases
    
    Mendeleev Commun., 13:3 (2003),  97–99
12. Chiral 1-alkoxyaziridines: resolution, nitrogen inversion, stucture and diastereomeric transformations
    
    Mendeleev Commun., 12:4 (2002),  137–140
13. Chiral drugs via the spontaneous resolution
    
    Mendeleev Commun., 12:1 (2002),  6–8
14. Outer-sphere association of hexacyanoferrate and nitrogen betaine anions
    
    Mendeleev Commun., 11:5 (2001),  181–182
15. Crystal properties of N-alkyl-substituted glycolurils as the precursors of chiral drugs
    
    Mendeleev Commun., 11:4 (2001),  134–136
16. Wedekind–Fock–Havinga salt Me(Et)N⁺(All)PhI^–·CHCl₃ as historically the first object for absolute asymmetric synthesis: spontaneous resolution, structure and absolute configuration
    
    Mendeleev Commun., 11:1 (2001),  1–5
17. Molecular structure of 1-methoxymethylaziridine and methoxymethyldimethylamine and anomeric effects
    
    Mendeleev Commun., 10:6 (2000),  217–220
18. Resolution of racemates with achiral reagents
    
    Mendeleev Commun., 10:3 (2000),  83–84
19. Spontaneous resolution of new conglomerates in the series of 4-arenesulfonyliminocyclohex-2-en-1-ones
    
    Mendeleev Commun., 10:1 (2000),  16–18
20. Optically active 2,2-dimethyl-1,3,4-triazabicyclo[4.1.0]heptan-5-one: synthesis, spontaneous resolution and absolute configuration
    
    Mendeleev Commun., 9:1 (1999),  26–27
21. Chiral glycouril, 2,6-diethyl-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione: spontaneous resolution, reactivity and absolute configuration
    
    Mendeleev Commun., 8:6 (1998),  231–233
22. Derivatives of 1-fluoroaziridine-2,2-dicarboxylic acid
    
    Mendeleev Commun., 7:2 (1997),  54–55
23. 3,4-Di-tert-butyl-l,3,4-oxadiazolidine: synthesis and structure
    
    Mendeleev Commun., 6:2 (1996),  69–71
24. A Superstable Nitrogen Pyramid: Stereodirected N-Halogenation of Methyl 2-Aziridinecarboxylate
    
    Mendeleev Commun., 5:6 (1995),  216–217
25. New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles
    
    Mendeleev Commun., 3:1 (1993),  21–23