Ткачев Алексей Васильевич

Публикации в базе данных Math-Net.Ru

1. Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives
   
   Mendeleev Commun., 29:5 (2019),  584–586
2. Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines
   
   Mendeleev Commun., 28:6 (2018),  584–586
3. Syntheses of chiral nopinane-annelated pyridines of C₂ and D₂-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9’-bi-4,5-diazafluorenylidene
   
   Mendeleev Commun., 27:2 (2017),  128–130
4. Syntheses of α-cyano substituted oximes from terpenic hydrocarbons via nitroso chlorides: X-ray structures of 3-cyanocaran-4-one oxime, 2-cyanopinan-3-one oxime and 1-cyano-p-menth-8-en-2-one oxime
   
   Mendeleev Commun., 25:2 (2015),  93–95
5. Stereoselective functionalisation of pinopyridine with anisidines and o-phenylenediamine
   
   Mendeleev Commun., 21:5 (2011),  253–255
6. Efficient synthesis of β-hydroxy sulfides by microwave-promoted ring opening in (+)-3-carene trans-epoxide with sodium thiolates
   
   Mendeleev Commun., 21:4 (2011),  192–193
7. First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.0^4,16]hexadeca-1,12-diene
   
   Mendeleev Commun., 19:5 (2009),  246–247
8. Mannich-type three component condensation of α-substituted caran-4-one oximes with formaldehyde and secondary amines
   
   Mendeleev Commun., 19:3 (2009),  139–140
9. Хироспецифический анализ летучих растительных веществ
   
   Усп. хим., 76:10 (2007),  1014–1033
10. Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro- 6H-benzo[c]quinolizine using the tert-amino effect
    
    Mendeleev Commun., 16:2 (2006),  82–83
11. C-Alkylation of nitroso chlorides with diethyl malonate: the X-ray structure of diethyl (±)-(1R^*,2S^*,5R^*)-2-{3(E)-hydroxyimino-2,6,6-trimethylbicyclo[3.1.1]-hept-2-yl}malonate
    
    Mendeleev Commun., 14:1 (2004),  18–20
12. Formation of an optically active 2-phenyl[1,2,4]triazolo[1,5-a]pyrimidine derivative in the reaction of (+)-3-carene-derived β-chlorovinylketone with benzylidene aminoguanidine
    
    Mendeleev Commun., 12:6 (2002),  226–227
13. Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime
    
    Mendeleev Commun., 12:3 (2002),  88–89
14. Transformation of myrtenoic acid nitrile to aminophospholene oxide by the reaction with dibenzylphosphine oxide: the X-ray structure of (1S*,2R*,6R*,8R*)-5-benzyl-9,9-dimethyl-5-oxo-4-phenyl- 5-phosphatricyclo[6.1.1.0^2,6]dec-3-en-3-ylamine
    
    Mendeleev Commun., 11:3 (2001),  98–99
15. New approach to [a]-fused fluoroquinolones: the synthesis of 5-oxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinolines
    
    Mendeleev Commun., 11:2 (2001),  53–54
16. N-Alkylation in the reactions of 5-imidazolylphenylthiourea with alkyl halides and chloroacetone
    
    Mendeleev Commun., 10:6 (2000),  233–235
17. Unusual acid-induced heterocyclisation of caryophyllene-type α-amino oximes: X-ray structure of (1S,2S,5R,8S)-1,4,4,8-tetramethyl-8-morpholin-4-yl-11-oxa-10-azatricyclo[7.2.2.0^2,5]tridec-9-ene
    
    Mendeleev Commun., 10:6 (2000),  211–212
18. Novel terpene-based chiral bis-α-aminooximes and the corresponding macrocycles: X-ray structure of a ring-fused 5,7-dioxa-1,4,8,11-tetraazacyclotrideca-3,8-diene derivative
    
    Mendeleev Commun., 10:6 (2000),  209–210
19. Nitrosochlorination of acyclic monoterpenoids
    
    Mendeleev Commun., 10:4 (2000),  146–148
20. Synthesis of chiral fused pyrimidines from (+)-3-carene- and limonene-derived isomeric β-enaminones
    
    Mendeleev Commun., 10:3 (2000),  112–114
21. Nitrosochlorination of cembrene
    
    Mendeleev Commun., 10:3 (2000),  109–111
22. A new ring transformation in the series of 1,2,3-thiadiazoles. Synthesis of 5H-[1,2,3]triazolo[5,1-b][1,3,4]thiadiazines
    
    Mendeleev Commun., 10:1 (2000),  19–20
23. Transformation of diaminocarane on a triosmium cluster. Absolute configuration of a cluster with a bridging imidyl ligand
    
    Mendeleev Commun., 9:6 (1999),  213–214
24. Synthesis of diethyl oxo phosphonates from monoterpene ketones – carvone, pinocarvone and 2-caren-4-one
    
    Mendeleev Commun., 7:4 (1997),  141–143
25. Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame
    
    Mendeleev Commun., 7:4 (1997),  139–141
26. Syntheses of novel chiral quinoxaline derivatives from seco-derivatives of monoterpene hydrocarbons 3-carene and α-pinene
    
    Mendeleev Commun., 7:3 (1997),  114–115
27. Synthesis of monoterpenic α-amino ketones
    
    Mendeleev Commun., 6:2 (1996),  64–66
28. New pyrazole-, isoxazole- and N-acylpyrazoline derivatives with a pinane carbon frame
    
    Mendeleev Commun., 6:1 (1996),  18–20
29. Synthesis of (–)-Caronaldehyde from ( + )-3-Carene
    
    Mendeleev Commun., 5:5 (1995),  179–180
30. Enaminones of the 2-Acetylcyclopent-1-en-1-ylamine Type Derived from the Terpenic Compounds Limonene, 3-Carene and δ-Cadinol
    
    Mendeleev Commun., 2:4 (1992),  161–162
31. An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime
    
    Mendeleev Commun., 2:3 (1992),  82–83
32. Is the Six-Membered Ring of the 3-Carene Molecule Planar?
    
    Mendeleev Commun., 1:3 (1991),  98–99