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Tolstikov Alexander Genrikhovich

Publications in Math-Net.Ru

  1. 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
  2. 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
  3. Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials of the classical reaction

    Usp. Khim., 77:2 (2008),  138–160
  4. Synthesis and cation-dependent photochromism of spironaphthoxazines obtained from crown-containing dihydroisoquinolines

    Mendeleev Commun., 16:6 (2006),  302–304
  5. 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
  6. Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances

    Usp. Khim., 73:6 (2004),  632–661
  7. Natural compounds in the synthesis of chiral organophosphorous ligands

    Usp. Khim., 72:9 (2003),  902–922
  8. Synthesis of tetracoordinated rhodium(I) complexes with chiral Shiff bases prepared from dehydroabietic acid

    Mendeleev Commun., 8:2 (1998),  60–62
  9. Natural polysulfides

    Usp. Khim., 66:9 (1997),  901–916
  10. Chiral organophosphorus ligands derived from the levopimaric acid-maleic anhydride adduct

    Mendeleev Commun., 6:6 (1996),  215–217
  11. Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates

    Mendeleev Commun., 6:4 (1996),  128–130
  12. Natural peroxides. Chemistry and biological activity

    Usp. Khim., 65:9 (1996),  836–851
  13. Natural aliphatic oxygenated unsaturated acids. Synthesis and biological activity.

    Usp. Khim., 65:5 (1996),  474–495
  14. A Short Route to Chiral Synthons: Preparation of Ketoeicosanoids with Hydropyrane Fragments

    Mendeleev Commun., 3:1 (1993),  18–20
  15. Glycals in enantiospecific synthesis

    Usp. Khim., 62:6 (1993),  621–643
  16. Synthesis of C21-(2R,3S,6R,4E)-2-N-Hexadecanoyl-6-hydroxysphingenine Dibenzoate

    Mendeleev Commun., 2:3 (1992),  108–110
  17. Stereocontrolled Synthesis of Modified Gaiactocerebroside

    Mendeleev Commun., 2:3 (1992),  96–97
  18. Enantiospecific Synthesis of (4S,5S)-5-Hydroxydecan-4-olide (L-Factor)

    Mendeleev Commun., 2:2 (1992),  53–54
  19. New Chirones Prepared from 2-Acetoxyglucal

    Mendeleev Commun., 1:4 (1991),  133–134
  20. 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
  21. Synthesis of Unsaturated Polyhydroxycarboxylic Acids as Structural Analogues of an Arachidonic Acid Metabolite

    Mendeleev Commun., 1:2 (1991),  52–53
  22. 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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