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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2011 |
1. |
A. G. Tolstikov, R. G. Savchenko, S. R. Afonkina, E. S. Lukina, D. V. Nedopekin, L. M. Khalilov, V. N. Odinokov, “Sodium borohydride reduction of 4-aryl-N-trifluoroacetyl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline ozonide”, Mendeleev Commun., 21:5 (2011), 285–286 |
1
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2008 |
2. |
A. V. Tarantin, V. A. Glushkov, O. A. Mayorova, I. A. Shcherbinina, A. G. Tolstikov, “The Povarov reaction of ethyl (18-carbomethoxyabieta-8,11,13-triene-12-imino)glyoxylate with electron-donating dienophiles”, Mendeleev Commun., 18:4 (2008), 188–190 |
10
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3. |
В. А. Глушков, А. Г. Толстиков, “Синтез замещенных 1,2,3,4-тетрагидрохинолинов c использованием реакции Поварова. Новые возможности классической реакции”, Усп. хим., 77:2 (2008), 138–160 ; V. A. Glushkov, A. G. Tolstikov, “Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials of the classical reaction”, Russian Chem. Reviews, 77:2 (2008), 137–159 |
166
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2006 |
4. |
V. V. Korolev, D. Yu. Vorobyev, E. M. Glebov, V. P. Grivin, V. F. Plyusnin, A. V. Koshkin, O. A. Fedorova, S. P. Gromov, M. V. Alfimov, Yu. V. Shklyaev, T. S. Vshivkova, Yu. S. Rozhkova, A. G. Tolstikov, V. A. Lokshin, A. Samat, “Synthesis and cation-dependent photochromism of spironaphthoxazines obtained from crown-containing dihydroisoquinolines”, Mendeleev Commun., 16:6 (2006), 302–304 |
7
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2005 |
5. |
Yu. V. Shklyaev, V. A. Glushkov, M. A. El'tsov, Yu. V. Gatilov, I. Yu. Bagryanskaya, A. G. Tolstikov, “Synthesis of regioisomeric (S)-(+)-3,3,4-trimethyl-8-methoxy-3,4-dihydrobenzo[h]isoquinolin-1(2H)-one and (S)-(+)-1,2,2-trimethyl-8-methoxy-1,2-dihydrobenzo[f]isoquinolin-4(3H)-one by the Ritter reaction”, Mendeleev Commun., 15:3 (2005), 125–127 |
4
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2004 |
6. |
В. А. Глушков, А. Г. Толстиков, “Хиральные 1,3,2-оксазаборолидины в асимметрическом синтезе: последние достижения”, Усп. хим., 73:6 (2004), 632–661 ; V. A. Glushkov, A. G. Tolstikov, “Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances”, Russian Chem. Reviews, 73:6 (2004), 581–608 |
42
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2003 |
7. |
А. Г. Толстиков, Т. Б. Хлебникова, О. В. Толстикова, Г. А. Толстиков, “Природные соединения в синтезе хиральных фосфорорганических лигандов”, Усп. хим., 72:9 (2003), 902–922 ; A. G. Tolstikov, T. B. Khlebnikova, O. V. Tolstikova, G. A. Tolstikov, “Natural compounds in the synthesis of chiral organophosphorous ligands”, Russian Chem. Reviews, 72:9 (2003), 803–822 |
31
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1998 |
8. |
A. G. Tolstikov, N. N. Karpyshev, Yu. I. Amosov, O. V. Tolstikova, T. B. Khlebnikova, G. A. Tolstikov, V. I. Mamatyuk, G. E. Salnikov, “Synthesis of tetracoordinated Rh(I) complexes with chiral shiff bases prepared from dehydroabietic acid”, Mendeleev Commun., 8:2 (1998), 60–62 |
1
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1997 |
9. |
Г. А. Толстиков, Э. Э. Шульц, А. Г. Толстиков, “Природные полисульфиды”, Усп. хим., 66:9 (1997), 901–916 ; G. A. Tolstikov, E. E. Shults, A. G. Tolstikov, “Natural polysulfides”, Russian Chem. Reviews, 66:9 (1997), 813–826 |
19
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1996 |
10. |
A. G. Tolstikov, O. V. Tolstikova, T. B. Khlebnikova, K. I. Zamaraev, V. G. Kasradze, O. S. Kukovinets, L. V. Spirikhin, “Chiral organophosphorus ligands derived from the levopimaric acid-maleic anhydride adduct”, Mendeleev Commun., 6:6 (1996), 215–217 |
3
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11. |
A. G. Tolstikov, O. V. Tolstikova, G. A. Tolstikov, “Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates”, Mendeleev Commun., 6:4 (1996), 128–130 |
2
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12. |
Г. А. Толстиков, А. Г. Толстиков, О. В. Толстикова, “Природные пероксиды. Химия и биологическая активность”, Усп. хим., 65:9 (1996), 836–851 ; G. A. Tolstikov, A. G. Tolstikov, O. V. Tolstikova, “Natural peroxides. Chemistry and biological activity”, Russian Chem. Reviews, 65:9 (1996), 769–783 |
21
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13. |
А. Г. Толстиков, Г. А. Толстиков, “Природные алифатические непредельные кислоты, содержащие кислородные функции. Синтез и биологическая активность”, Усп. хим., 65:5 (1996), 474–495 ; A. G. Tolstikov, G. A. Tolstikov, “Natural aliphatic oxygenated unsaturated acids. Synthesis and biological activity.”, Russian Chem. Reviews, 65:5 (1996), 441–459 |
2
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1993 |
14. |
A. G. Tolstikov, E. E. Savateeva, N. V. Khakhalina, L. V. Spirikhin, V. R. Sultanmuratova, G. A. Tolstikov, “A Short Route to Chiral Synthons: Preparation of Ketoeicosanoids with Hydropyrane Fragments”, Mendeleev Commun., 3:1 (1993), 18–20 |
1
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15. |
А. Г. Толстиков, Г. А. Толстиков, “Гликали в энантиоспецифическом синтезе”, Усп. хим., 62:6 (1993), 621–643 ; A. G. Tolstikov, G. A. Tolstikov, “Glycals in enantiospecific synthesis”, Russian Chem. Reviews, 62:6 (1993), 579–601 |
44
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1992 |
16. |
A. G. Tolstikov, R. Kh. Yamilov, L. V. Spirikhin, G. A. Tolstikov, “Synthesis of C<sub>21</sub>-(2R,3S,6R,4E)-2-N-Hexadecanoyl-6-hydroxysphingenine Dibenzoate”, Mendeleev Commun., 2:3 (1992), 108–110 |
2
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17. |
A. G. Tolstikov, R. Kh. Yamilov, O. F. Prokopenko, G. A. Tolstikov, “Stereocontrolled Synthesis of Modified Galactocerebroside”, Mendeleev Commun., 2:3 (1992), 96–97 |
3
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18. |
A. G. Tolstikov, R. Kh. Yamilov, N. V. Khakhalina, E. E. Savateeva, L. V. Spirikhin, G. A. Tolstikov, “Enantiospecific Synthesis of (4S,5S)-5-Hydroxydecan-4-olide (L-Factor)”, Mendeleev Commun., 2:2 (1992), 53–54 |
4
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1991 |
19. |
A. G. Tolstikov, E. E. Savateeva, L. V. Spirikhin, G. A. Tolstikov, “New Chirones Prepared from 2-Acetoxyglucal”, Mendeleev Commun., 1:4 (1991), 133–134 |
3
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20. |
A. G. Tolstikov, O. F. Prokopenko, R. Kh. Yamilov, G. A. Tolstikov, “A Convenient Approach to the Synthesis of Glycosphingolipids via the Acidic Decyclization of Hexo-O-acetyl-D-gentiobial”, Mendeleev Commun., 1:2 (1991), 64–65 |
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21. |
A. G. Tolstikov, O. F. Prokopenko, L. M. Khalilov, L. V. Spirikhin, A. A. Berg, V. R. Sultanmuratova, G. A. Tolstikov, “Synthesis of Unsaturated Polyhydroxycarboxylic Acids as Structural Analogues of an Arachidonic Acid Metabolite”, Mendeleev Commun., 1:2 (1991), 52–53 |
1
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22. |
A. G. Tolstikov, O. F. Prokopenko, L. M. Khalilov, L. V. Spirikhin, G. A. Tolstikov, “Synthesis and Acid-induced Ring Opening of Modified Glycals. Synthons for (14R,15R)-Lipoxin B and (7S,8R)-(–)-Disparlure”, Mendeleev Commun., 1:2 (1991), 51 |
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