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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2019 |
| 1. |
E. S. Vasilyev, S. N. Bizyaev, V. Yu. Komarov, A. V. Tkachev, “Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives”, Mendeleev Commun., 29:5 (2019), 584–586   |
3
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2018 |
| 2. |
Yu. P. Ustimenko, A. M. Agafontsev, V. Yu. Komarov, A. V. Tkachev, “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 |
10
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2017 |
| 3. |
E. S. Vasilyev, I. Yu. Bagryanskaya, A. V. Tkachev, “Syntheses of chiral nopinane-annelated pyridines of C<sub>2</sub> and D<sub>2</sub>-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 |
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2015 |
| 4. |
S. N. Bizyaev, Yu. V. Gatilov, A. V. Tkachev, “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 |
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2011 |
| 5. |
E. S. Vasilyev, A. M. Agafontsev, V. D. Kolesnik, Yu. V. Gatilov, A. V. Tkachev, “Stereoselective functionalisation of pinopyridine with anisidines and o-phenylenediamine”, Mendeleev Commun., 21:5 (2011), 253–255 |
4
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| 6. |
A. M. Agafontsev, N. B. Gorshkov, A. V. Tkachev, “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 |
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2009 |
| 7. |
A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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<sup>4,16</sup>]hexadeca-1,12-diene”, Mendeleev Commun., 19:5 (2009), 246–247 |
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| 8. |
N. B. Gorshkov, A. M. Agafontsev, Yu. V. Gatilov, A. V. Tkachev, “Mannich-type three component condensation of α-substituted caran-4-one oximes with formaldehyde and secondary amines”, Mendeleev Commun., 19:3 (2009), 139–140 |
2
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2007 |
| 9. |
А. В. Ткачев, “Хироспецифический анализ летучих растительных веществ”, Усп. хим., 76:10 (2007), 1014–1033  ; A. V. Tkachev, “Chirospecific analysis of plant volatiles”, Russian Chem. Reviews, 76:10 (2007), 951–969  |
12
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2006 |
| 10. |
E. V. Deeva, T. V. Glukhareva, A. V. Tkachev, Yu. Yu. Morzherin, “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 |
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2004 |
| 11. |
S. N. Bizjaev, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “C-Alkylation of nitroso chlorides with diethyl malonate: the X-ray structure of diethyl (±)-(1R<sup>*</sup>,2S<sup>*</sup>,5R<sup>*</sup>)-2-{3(E)-hydroxyimino-2,6,6-trimethylbicyclo[3.1.1]-hept-2-yl}malonate”, Mendeleev Commun., 14:1 (2004), 18–20 |
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2002 |
| 12. |
S. A. Popov, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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 |
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| 13. |
A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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 |
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2001 |
| 14. |
V. D. Kolesnik, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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<sup>2,6</sup>]dec-3-en-3-ylamine”, Mendeleev Commun., 11:3 (2001), 98–99 |
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| 15. |
E. Tsoi, V. N. Charushin, E. V. Nosova, G. N. Lipunova, A. V. Tkachev, “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 |
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2000 |
| 16. |
O. S. Eltsov, V. S. Mokrushin, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “N-Alkylation in the reactions of 5-imidazolylphenylthiourea with alkyl halides and chloroacetone”, Mendeleev Commun., 10:6 (2000), 233–235 |
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| 17. |
A. V. Tkachev, A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, “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<sup>2,5</sup>]tridec-9-ene”, Mendeleev Commun., 10:6 (2000), 211–212 |
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| 18. |
P. A. Petukhov, I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Tkachev, “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 |
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| 19. |
Ya. V. Markova, A. V. Tkachev, “Nitrosochlorination of acyclic monoterpenoids”, Mendeleev Commun., 10:4 (2000), 146–148 |
2
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| 20. |
S. A. Popov, A. V. Tkachev, “Synthesis of chiral fused pyrimidines from (+)-3-carene- and limonene-derived isomeric β-enaminones”, Mendeleev Commun., 10:3 (2000), 112–114 |
2
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| 21. |
A. V. Tkachev, A. V. Vorobjev, “Nitrosochlorination of cembrene”, Mendeleev Commun., 10:3 (2000), 109–111 |
4
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| 22. |
Yu. Yu. Morzherin, T. V. Glukhareva, I. N. Slepukhina, V. S. Mokrushin, A. V. Tkachev, V. A. Bakulev, “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 |
12
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1999 |
| 23. |
V. A. Maksakov, V. P. Kirin, A. V. Virovets, P. A. Petukhov, A. V. Tkachev, “Transformation of diaminocarane on a triosmium cluster. Absolute configuration of a cluster with a bridging imidyl ligand”, Mendeleev Commun., 9:6 (1999), 213–214 |
3
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1997 |
| 24. |
V. D. Kolesnik, M. M. Shakirov, A. V. Tkachev, “Synthesis of diethyl oxo phosphonates from monoterpene ketones – carvone, pinocarvone and 2-caren-4-one”, Mendeleev Commun., 7:4 (1997), 141–143 |
12
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| 25. |
S. A. Popov, A. V. Tkachev, “Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame”, Mendeleev Commun., 7:4 (1997), 139–141 |
1
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| 26. |
A. V. Korovin, A. V. Rukavishnikov, A. V. Tkachev, “Syntheses of novel chiral quinoxaline derivatives from seco-derivatives of monoterpene hydrocarbons 3-carene and α-pinene”, Mendeleev Commun., 7:3 (1997), 114–115 |
4
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1996 |
| 27. |
P. A. Petukhov, A. V. Tkachev, “Synthesis of monoterpenic α-amino ketones”, Mendeleev Commun., 6:2 (1996), 64–66 |
5
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| 28. |
A. M. Chibiryaev, S. A. Popov, A. V. Tkachev, “New pyrazole-, isoxazole- and N-acylpyrazoline derivatives with a pinane carbon frame”, Mendeleev Commun., 6:1 (1996), 18–20 |
10
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1995 |
| 29. |
V. D. Kolesnik, A. V. Rukavishnikov, A. V. Tkachev, “Synthesis of (–)-Caronaldehyde from ( + )-3-Carene”, Mendeleev Commun., 5:5 (1995), 179–180 |
4
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1992 |
| 30. |
A. V. Tkachev, A. V. Rukavishnikov, “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 |
11
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| 31. |
A. M. Chibiryaev, I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Tkachev, “An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime”, Mendeleev Commun., 2:3 (1992), 82–83 |
1
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1991 |
| 32. |
A. V. Tkachev, A. Yu. Denisov, “Is the Six-Membered Ring of the 3-Carene Molecule Planar?”, Mendeleev Commun., 1:3 (1991), 98–99 |
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