Chervin Ivan Ivanovich

Publications in Math-Net.Ru

1. Simple chiral auxiliary-assisted resolution of 2-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid
   
   Mendeleev Commun., 20:5 (2010),  291–292
2. Absolute configuration of a chiral proton sponge
   
   Mendeleev Commun., 18:2 (2008),  86–87
3. Methanetriacetic and methylmethanetriacetic acids, their precursors and derivatives: NMR and X-ray diffraction studies
   
   Mendeleev Commun., 15:5 (2005),  187–189
4. Nitrogen chirality via the sterical veto of N inversion
   
   Mendeleev Commun., 13:3 (2003),  136–139
5. Sterically hindered nitrogen inversion in five-membered cyclic hydrazines
   
   Mendeleev Commun., 12:5 (2002),  189–193
6. 2,5-Diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylic acids: synthesis, resolution, absolute configuration and crystal structures of the racemic and (–)-enantiomeric forms
   
   Mendeleev Commun., 9:3 (1999),  109–111
7. 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
8. 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
9. α,α’-Diamino-α,α’-dicarboxyadipic acid tetraester: synthesis, lactamisation and dilactam structure
   
   Mendeleev Commun., 8:6 (1998),  228–230
10. Sterically controlled population of the 1,2-cis-form of 1,2-dimethyl-3-tert-butyldiaziridine
    
    Mendeleev Commun., 8:3 (1998),  113–116
11. Methyl 2-trifluoromethylaziridine-2-carboxylate: stereodirected N-halogenation from the sterically more hindered side
    
    Mendeleev Commun., 7:6 (1997),  229–230
12. Stereocontrolled synthesis and cyclization of (+,−)-α,α’-dihydroxy-α,α ’, β-trimethylglutaric acid derivatives
    
    Mendeleev Commun., 7:2 (1997),  64–66
13. Unusual reaction of aziridine dimer with acetylene dicarboxylates
    
    Mendeleev Commun., 7:2 (1997),  56–58
14. Derivatives of 1-fluoroaziridine-2,2-dicarboxylic acid
    
    Mendeleev Commun., 7:2 (1997),  54–55
15. Autoassembling of the quinuclidine nucleus: one-step synthesis, structure and properties of dimethyl 4-hydroxy-6,6,7,7-tetramethyl-Δ²-dehydroquinuclidine-2,3-di-carboxylate
    
    Mendeleev Commun., 6:4 (1996),  143–145
16. Heterolytic fragmentation of 4-hydroxy-6,6,7,7-tetramethyl-Δ²-dehydro-quinuclidine-2,3-dicarboxylic acid esters
    
    Mendeleev Commun., 6:3 (1996),  108–110
17. 1,2-Di-tert-butyldiaziridine
    
    Mendeleev Commun., 6:3 (1996),  106–107
18. 3,4-Di-tert-butyl-l,3,4-oxadiazolidine: synthesis and structure
    
    Mendeleev Commun., 6:2 (1996),  69–71
19. A Superstable Nitrogen Pyramid: Stereodirected N-Halogenation of Methyl 2-Aziridinecarboxylate
    
    Mendeleev Commun., 5:6 (1995),  216–217
20. New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles
    
    Mendeleev Commun., 3:1 (1993),  21–23
21. Synthesis and Properties of 2,3-Dimethoxy-1,4,2,3-dioxadiazinane and Dialkoxydiazene Oxides
    
    Mendeleev Commun., 2:2 (1992),  50–51
22. Is there Ring–Chain Tautomerism in γ-Nitrosoalkanols?
    
    Mendeleev Commun., 1:1 (1991),  9–10