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Publications in Math-Net.Ru |
Citations |
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2018 |
| 1. |
K. E. Metlushka, D. N. Sadkova, K. A. Nikitina, Z. R. Yamaleeva, K. A. Ivshin, O. N. Kataeva, V. A. Alfonsov, “A new synthetic route to chiral 3-aryl-5-ethyl-1,4,2-oxazaphosphorines”, Mendeleev Commun., 28:6 (2018), 579–581 |
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2016 |
| 2. |
K. A. Nikitina, K. E. Metlushka, D. N. Sadkova, L. N. Shaimardanova, V. A. Alfonsov, “Synthesis of α-amino phosphonates by diastereoselective addition of diethyl phosphite sodium salt to aldimines derived from Betti base”, Mendeleev Commun., 26:5 (2016), 395–396 |
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2010 |
| 3. |
M. A. Pudovik, L. K. Kibardina, S. A. Terent'eva, A. R. Burilov, O. N. Kataeva, G. A. Chmutova, Sh. K. Latypov, O. G. Sinyashin, V. A. Alfonsov, “Stereospecific cascade cyclization reaction with the formation of tetracyclic hexacoordinated phosphorus derivatives”, Mendeleev Commun., 20:4 (2010), 226–228 |
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2007 |
| 4. |
L. K. Kibardina, M. A. Pudovik, V. A. Alfonsov, O. N. Kataeva, “Synthesis of enantiopure 1,3,4-thiazaphospholes”, Mendeleev Commun., 17:6 (2007), 323–324 |
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| 5. |
V. F. Zheltukhin, K. E. Metlushka, D. N. Sadkova, Ch. E. McKenna, B. A. Kashemirov, V. A. Alfonsov, “A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors”, Mendeleev Commun., 17:4 (2007), 239–240 |
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2005 |
| 6. |
V. L. Mamedova, K. A. Nikitina, V. E. Kataev, V. A. Alfonsov, “Methyl <i>ent</i>-16α-dichlorophosphitobeyeran-19-oate as the first example of phosphorylated diterpenoid derivatives of the beyerane series”, Mendeleev Commun., 15:3 (2005), 98–99 |
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| 7. |
O. I. Militsina, G. I. Kovyljaeva, G. A. Bakaleynik, I. Yu. Strobykina, V. E. Kataev, V. A. Alfonsov, R. Z. Musin, D. V. Beskrovny, I. A. Litvinov, “Transformation of isosteviol oxime to a lactone under Beckmann reaction conditions”, Mendeleev Commun., 15:1 (2005), 27–29 |
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2004 |
| 8. |
M. N. Dimukhametov, M. A. Abaskalova, E. Yu. Davydova, E. V. Bayandina, A. B. Dobrynin, I. A. Litvinov, V. A. Alfonsov, “Reactions of sodium <i>N</i>-benzylideneglycinate with dialkyl chlorophosphites: formation of 1,4-bis[α-(dialkoxyphosphoryl)benzyl]piperazine-2,5-diones”, Mendeleev Commun., 14:1 (2004), 35–37 |
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2003 |
| 9. |
V. A. Alfonsov, O. V. Andreeva, G. A. Bakaleynik, D. V. Beskrovny, V. E. Kataev, G. I. Kovyljaeva, I. A. Litvinov, O. I. Militsina, “Unexpected bromination reaction of isosteviol methyl ester with bromoalkanes”, Mendeleev Commun., 13:5 (2003), 234–235 |
14
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| 10. |
M. N. Dimukhametov, E. V. Bayandina, E. Yu. Davydova, A. T. Gubaidullin, V. A. Alfonsov, “A stereochemical approach to the Kabachnik–Fields reaction mechanism”, Mendeleev Commun., 13:3 (2003), 150–151 |
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2001 |
| 11. |
M. N. Dimukhametov, E. Yu. Davydova, E. V. Bayandina, A. B. Dobrynin, I. A. Litvinov, V. A. Alfonsov, “Stereospecific intramolecular cyclization of diethyl (<i>R</i>)-2-(<i>N</i>-benzylidene)-aminobutyl phosphite into (3<i>R</i>,5<i>R</i>)-2-ethoxy-2-oxo-3-phenyl-5-ethyl-1,4,2-oxazaphosphorinane in the presence of hydrogen chloride”, Mendeleev Commun., 11:6 (2001), 222–224 |
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| 12. |
M. N. Dimukhametov, E. V. Bayandina, E. Yu. Davydova, A. B. Dobrynin, A. T. Gubaidullin, I. A. Litvinov, V. A. Alfonsov, “An alternative reaction of <i>ortho</i>-(<i>N</i>-benzylidene)aminophenol with chlorophosphites: formation of 2-(2’-alkoxy)-2-oxo-3-phenyl-5,6-benzo-1,4,2-oxazaphosphorinanes”, Mendeleev Commun., 11:5 (2001), 196–197 |
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2000 |
| 13. |
V. A. Alfonsov, G. A. Bakaleynik, A. T. Gubaidullin, V. E. Kataev, G. I. Kovyljaeva, A. I. Konovalov, I. A. Litvinov, I. Yu. Strobykina, O. V. Andreeva, M. G. Korochkina, “The first example of the supramolecular regulation of amidophosphite reactivity”, Mendeleev Commun., 10:5 (2000), 177–178 |
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1999 |
| 14. |
V. A. Alfonsov, G. A. Bakaleynik, A. T. Gubaidullin, V. E. Kataev, G. I. Kovyljaeva, A. I. Konovalov, I. A. Litvinov, I. Yu. Strobykina, O. V. Andreeva, M. G. Korochkina, “Molecular complex of isosteviol with aniline”, Mendeleev Commun., 9:6 (1999), 227–228 |
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