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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2018 |
| 1. |
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  |
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2011 |
| 2. |
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 |
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| 3. |
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 |
4
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2009 |
| 4. |
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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| 5. |
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 |
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2002 |
| 6. |
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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2000 |
| 7. |
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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