Мифтахов Мансур Сагарьярович

Публикации в базе данных Math-Net.Ru

1. A facile synthesis of (±)-15-deoxy-Δ^12,14-prostaglandin J₂ methyl ester
   
   Mendeleev Commun., 33:4 (2023),  479–480
2. Cytotoxicity of novel cross-conjugated arylated cyclopentene-1,3-diones
   
   Mendeleev Commun., 32:2 (2022),  183–185
3. Lead tetraacetate assisted formation of bis(acetoxy)acetic acid derivative from carvone
   
   Mendeleev Commun., 31:5 (2021),  696–697
4. Formal synthesis of J-type prostaglandins based on enantiopure polyfunctional cyclopentenol derivative
   
   Mendeleev Commun., 31:2 (2021),  239–241
5. Base-determinant chemodivergent transformations of chiral 2,3-dibromopropanamide derivative
   
   Mendeleev Commun., 30:3 (2020),  313–314
6. A convenient synthesis of enantiopure (4aS,7aR)-1,4,4a,7a-tetrahydrocyclopenta[c]pyran-3,7-dione
   
   Mendeleev Commun., 30:1 (2020),  10–11
7. Simple antitumor model compounds for cross-conjugated cyclopentenone prostaglandins
   
   Mendeleev Commun., 29:4 (2019),  372–374
8. 2,3,5-Trichlorocyclopent-2-enone derivatives in the Friedel–Crafts reaction with methoxybenzenes and the anticancer activity of the products
   
   Mendeleev Commun., 29:2 (2019),  174–175
9. Enantiopure vicinally trisubstituted all-cis-bis(hydroxymethyl)-cyclopentenols and their derivatives
   
   Mendeleev Commun., 28:5 (2018),  546–547
10. Synthetically attractive chiral cyclopentenone building blocks conjugated with tetrahydro- and 2-oxotetrahydrofurans
    
    Mendeleev Commun., 28:4 (2018),  362–363
11. Self-condensation of N-substituted (4H-thieno[3,2-b]-pyrrol-5-yl)methanols into bis(thienopyrrolyl)methanes
    
    Mendeleev Commun., 28:2 (2018),  192–194
12. Novel azetidinones for carbapenems and fragmentation in the allylamine precursor analogue
    
    Mendeleev Commun., 28:2 (2018),  131–132
13. Straightforward synthesis of pyrrolizidines
    
    Mendeleev Commun., 27:2 (2017),  163–165
14. Side-modified 15-deoxy-Δ^12,14-prostaglandin D₂, precursor of corresponding PGJ₂. Synthesis from cloprostenol and anticancer activity
    
    Mendeleev Commun., 27:2 (2017),  125–127
15. Synthesis of racemic Entecavir
    
    Mendeleev Commun., 27:1 (2017),  12–13
16. Intermolecular disproportionation between dimethyl (2-furylmethylidene)malonate and 4-methoxybenzylamine
    
    Mendeleev Commun., 26:5 (2016),  429–430
17. A short synthesis of the carbocyclic core of Entecavir from Corey lactone
    
    Mendeleev Commun., 26:1 (2016),  9–10
18. Acrylate and methacrylate derivatives of fullerenes as electron-selective buffer layer materials for inverted organic solar cells
    
    Mendeleev Commun., 25:5 (2015),  348–349
19. Synthesis and ring-opening metathesis polymerization of fullerene-containing α,ω-bis-norbornenes
    
    Mendeleev Commun., 25:3 (2015),  202–203
20. Synthesis of the C⁶–C²¹ fragment of epothilone analogues
    
    Mendeleev Commun., 24:6 (2014),  372–373
21. Unexpected fragmentation of 16β-acetoxy-22-oxocholestanes on the action of methylenetriphenylphosphorane
    
    Mendeleev Commun., 24:5 (2014),  272–273
22. New α-methylidenecyclopentenone block from Corey lactone diol
    
    Mendeleev Commun., 23:6 (2013),  321–322
23. Фотопреобразователи солнечной энергии на основе тонких пленок органических материалов
    
    Письма в ЖТФ, 39:19 (2013),  25–31
24. Synthesis of fullerene-containing methacrylates
    
    Mendeleev Commun., 22:4 (2012),  199–200
25. Efficient Resolution of Some Monoprotected Derivatives of Corey Lactone
    
    Mendeleev Commun., 22:3 (2012),  125–126
26. Triethylsilyl triflate-promoted skeletal rearrangement of bottrospicatols
    
    Mendeleev Commun., 21:3 (2011),  140–141
27. Chiral building blocks from R-(–)-carvone: N-bromosuccinimidemediated addition–sceletal rearrangement of (–)-cis-carveol
    
    Mendeleev Commun., 20:2 (2010),  77–79
28. Synthesis of enantiomeric cyclosarcomycins
    
    Mendeleev Commun., 20:1 (2010),  15–16
29. Enantiomeric 4,4a,7,7a-tetrahydro-1H-cyclopenta[c]pyran-3-ones
    
    Mendeleev Commun., 19:5 (2009),  275
30. Synthesis of the thiazole-containing C¹¹–C²¹-block of a gem-dimethylcyclopropane derivative of epothilones
    
    Mendeleev Commun., 19:5 (2009),  248–249
31. Efficient one-pot synthesis of chlorinated cyclopentenones from hexachlorocyclopentadiene
    
    Mendeleev Commun., 17:5 (2007),  306–307
32. Double α-ketol rearrangement of (1S,2R,4R)-2-acetyl-1-vinyl-2-hydroxy-7,7-dimethylbicyclo[2.2.1]heptane
    
    Mendeleev Commun., 16:2 (2006),  111–112
33. New ‘substitution–recyclization’ reaction of a tetrachlorocyclopentadienone dimer with amines
    
    Mendeleev Commun., 13:5 (2003),  232–233
34. A ‘substrate-divergent’ approach to chiral cyclopentanes and cyclohexanes from a common precursor based on levoglucosan
    
    Mendeleev Commun., 13:3 (2003),  153–154
35. Chiral synthetic block based on (R)-pantolactone
    
    Mendeleev Commun., 13:3 (2003),  151–152
36. Тандемные превращения, инициируемые и определяемые реакцией Михаэля
    
    Усп. хим., 69:12 (2000),  1091–1110
37. Enantiomeric 9,11-Dideoxy-9,11-ethane Analogues of Prostaglandin Endoperoxide
    
    Mendeleev Commun., 4:2 (1994),  45–47
38. Левоглюкозенон: свойства, реакции и использование в тонком органическом синтезе
    
    Усп. хим., 63:10 (1994),  922–936
39. Морские простаноиды
    
    Усп. хим., 63:6 (1994),  543–555
40. A Total Decyclisation of Jaeschkeanadiol
    
    Mendeleev Commun., 3:6 (1993),  253–254
41. A Novel Approach to Carbacycline
    
    Mendeleev Commun., 2:1 (1992),  4–6
42. Unusual Reactions of 2,3,5-Trichloro-4,4-dimethoxy-5-allylcyclopent-2-en-1-one with Amines
    
    Mendeleev Commun., 1:4 (1991),  149–151