Beletskaya Irina Petrovna

Publications in Math-Net.Ru

1. Palladium-catalyzed amination in the synthesis of novel fluorescent sensors based on 3,3'-diamino substituted 1,1'-bi(2-naphthol)
   
   Mendeleev Commun., 35:1 (2025),  11–13
2. Polymerization–cyclodepolymerization of polypropylene carbonate mediated by cobalt catalyst
   
   Mendeleev Commun., 34:6 (2024),  878–880
3. Synthesis of acrylic acid and acrylates from CO₂ and ethylene — the thorny path from dream to reality
   
   Usp. Khim., 93:9 (2024),  1–22
4. From epoxides and carbon dioxide to polycarbonates: synthesis, properties and applications
   
   Usp. Khim., 93:2 (2024),  1–48
5. Carbon dioxide and "methanol" economy: advances in the catalytic synthesis of methanol from CO₂
   
   Usp. Khim., 93:1 (2024),  1–45
6. The green chemistry paradigm in modern organic synthesis
   
   Usp. Khim., 92:12 (2023),  1–187
7. A comparison of homogeneous and heterogeneous copper catalyzed arylation of amines
   
   Mendeleev Commun., 32:1 (2022),  91–93
8. Photoredox-copper catalyzed Meerwein cyanoarylation of styrenes
   
   Mendeleev Commun., 31:6 (2021),  815–817
9. A convenient one-pot two-step synthesis of pyrazolylphosphonates from ethynylphosphonate
   
   Mendeleev Commun., 31:4 (2021),  536–537
10. Synthesis of novel cytotoxic 3-azolylsteroids via Cu-catalyzed C–N coupling
    
    Mendeleev Commun., 31:3 (2021),  359–361
11. Metal-catalyzed reactions for the C(sp$^{2}$)–N bond formation: achievements of recent years
    
    Usp. Khim., 90:11 (2021),  1359–1396
12. Catalysis and regioselectivity in hydrofunctionalization reactions of unsaturated carbon bonds. Part III
    
    Usp. Khim., 90:1 (2021),  70–93
13. Catalysis and regioselectivity in hydrofunctionalization reactions of unsaturated carbon bonds. Part II. Hydroamination
    
    Usp. Khim., 89:10 (2020),  1074–1114
14. Gold as a catalyst. Part III. Addition to double bonds
    
    Usp. Khim., 89:5 (2020),  491–536
15. Catalysis and regioselectivity in hydrofunctionalization reactions of unsaturated carbon bonds. Part I
    
    Usp. Khim., 89:2 (2020),  250–274
16. Efficient and stereoselective synthesis of (S)-α-propargylglycine derivatives from allenylboronic acid
    
    Mendeleev Commun., 29:5 (2019),  498–499
17. Enhanced catalytic activity of CuI/diethoxyphosphoryl-1,10-phenanthrolines in ‘on water’ Cu-catalyzed Sonogashira reaction
    
    Mendeleev Commun., 29:4 (2019),  378–379
18. Friedel–Crafts reaction of electron-rich (het)arenes with nitroalkenes
    
    Mendeleev Commun., 29:2 (2019),  138–139
19. Chiral inducers with (1R,2R)-1,2-diaminocyclohexane core for organo- and metallocatalysis
    
    Mendeleev Commun., 29:1 (2019),  35–37
20. Room temperature MgI₂-catalyzed Friedel–Crafts reaction between electron-rich (het)arenes and ethyl glyoxylate
    
    Mendeleev Commun., 28:4 (2018),  429–430
21. Regioselective N¹- or N²-modification of benzotriazoles with iodonium salts in the presence of copper compounds
    
    Mendeleev Commun., 28:3 (2018),  287–289
22. Highly efficient Sandmeyer reaction on immobilized Cu^I/Cu^II-based catalysts
    
    Mendeleev Commun., 28:3 (2018),  261–263
23. Gold as a catalyst. Part II. Alkynes in the reactions of carbon–carbon bond formation
    
    Usp. Khim., 87:10 (2018),  984–1047
24. Organoelement chemistry: promising growth areas and challenges
    
    Usp. Khim., 87:5 (2018),  393–507
25. Phosphine-catalyzed [3 + 2] cycloaddition of ethyl buta-2,3-dienoate to adamantane-containing N-substituted maleimides
    
    Mendeleev Commun., 27:6 (2017),  550–552
26. Gold as a catalyst. Part I. Nucleophilic addition to the triple bond
    
    Usp. Khim., 86:8 (2017),  689–749
27. Poly(ethylene glycol)-supported chiral pyridine-2,6-bis(oxazoline): synthesis and application as a recyclable ligand in Cuⁱ-catalyzed enantioselective direct addition of terminal alkynes to imines
    
    Mendeleev Commun., 26:6 (2016),  477–479
28. Heterogeneous Jørgensen–Hayashi catalyst for asymmetric Michael addition of malonates to α,β-enals. Cooperative effect with Ca(OTf)₂
    
    Mendeleev Commun., 26:6 (2016),  469–470
29. Catalytic amination in the synthesis of hybrid polymacrocycles comprising porphyrin and azacrown ether moieties
    
    Mendeleev Commun., 26:3 (2016),  199–201
30. Synthetic routes to 3(5)-phosphonylated pyrazoles
    
    Usp. Khim., 85:7 (2016),  667–683
31. Activated carbon as an efficient support for gold nanoparticles that catalyze the hydrogenation of nitro compounds with molecular hydrogen
    
    Mendeleev Commun., 25:6 (2015),  443–445
32. Polymer-immobilized α,α-bis[bis-3,5-(trifluoromethyl)phenyl]prolinol silyl ether: synthesis and application in the asymmetric α-amination of aldehydes
    
    Mendeleev Commun., 25:6 (2015),  410–411
33. Cu^I-mediated modification of polyamines with fluorophore groups
    
    Mendeleev Commun., 25:4 (2015),  245–247
34. Simple and efficient Au^I-based catalyst for hydroamination of alkynes
    
    Mendeleev Commun., 24:6 (2014),  332–333
35. Optical methods for the detection of heavy metal ions
    
    Usp. Khim., 83:3 (2014),  196–224
36. Nucleophilic substitution at the halogen atom (halogenophilic reactions)
    
    Usp. Khim., 81:4 (2012),  317–335
37. An expedient synthesis of diethyl diazomethylphosphonate
    
    Mendeleev Commun., 21:3 (2011),  142–143
38. Synthesis of tethered bis-macrocycles by cross-coupling of N-(3,5-dibromobenzyl)azacrowns with α,ω-diamino compounds
    
    Mendeleev Commun., 21:3 (2011),  132–133
39. Organocatalytic Michael and Friedel–Crafts reactions in enantioselective synthesis of biologically active compounds
    
    Usp. Khim., 80:11 (2011),  1119–1165
40. Novel photochromic 3-(3-coumarinyl)-4-(3-thienyl)maleic acid cyclic derivatives
    
    Mendeleev Commun., 20:1 (2010),  22–24
41. Pd-catalyzed amination of isomeric dibromobiphenyls: possibilities of one-step synthesis of macrocycles
    
    Mendeleev Commun., 20:1 (2010),  1–3
42. Catalysis as an important tool of green chemistry
    
    Usp. Khim., 79:6 (2010),  493–515
43. Pd-catalyzed amination in the synthesis of a new family of polyazamacrocycles containing 1,3-disubstituted adamantane moieties
    
    Mendeleev Commun., 19:3 (2009),  136–138
44. Organocatalysis of asymmetric aldol reaction. Catalysts and reagents
    
    Usp. Khim., 78:8 (2009),  796–845
45. Catalytic synthesis and transformations of organophosphorus compounds
    
    Mendeleev Commun., 18:3 (2008),  113–120
46. Arylamidate palladium complexes containing deprotonated phthalimide and p-methylbenzamide: possibility of their participation in reductive elimination
    
    Mendeleev Commun., 17:3 (2007),  142–144
47. Tetrachloroethylene from methane and carbon tetrachloride: a new approach to the utilization of toxic organochlorine waste
    
    Mendeleev Commun., 16:6 (2006),  312–313
48. Catalytic thiocyanation of aryldiazonium salts in the presence of copper salts
    
    Mendeleev Commun., 16:5 (2006),  250–251
49. Crystal structure of diaqua[N,N′-bis(tetrafluoropyridyl)diaza-18-crown-6]lead(II) perchlorate: the effect of perfluoroaromatic groups on the stucture of the complex
    
    Mendeleev Commun., 16:3 (2006),  147–149
50. Synthesis of trifluoromethyl-containing depsipeptides via OH insertion of rhodium carbenoid into the carboxylic group of N-protected α-amino acids
    
    Mendeleev Commun., 15:6 (2005),  222–223
51. Solvent-free Pd-catalysed N-arylation of amines, amides and diaza-18-crown-6
    
    Mendeleev Commun., 13:4 (2003),  158–160
52. Bi-and trinuclear σ-aryl complexes of iron and manganese
    
    Mendeleev Commun., 13:2 (2003),  43–45
53. Unusual magnesium–anthracene adduct
    
    Mendeleev Commun., 12:3 (2002),  108–109
54. Preparation of unsymmetrical diaryl selenides in nucleophilic substitution reactions with activated aryl fluorides
    
    Mendeleev Commun., 10:6 (2000),  213–214
55. Selective bromination of alkanes and arylalkanes with CBr₄
    
    Mendeleev Commun., 10:5 (2000),  175–176
56. (η⁶-Naphthalene)tricarbonylchromium-mediated hydrogenation of 3,5-diene-1,7-diynes as a route to (Z,Z,Z)-1,4,7-trienes
    
    Mendeleev Commun., 10:5 (2000),  168–170
57. Synthesis of selenoesters
    
    Mendeleev Commun., 10:4 (2000),  127–128
58. Synthesis and properties of functionalised dendrimers
    
    Usp. Khim., 69:8 (2000),  699–720
59. Generation of platinum(III) species by mechanical treatment of solid K₂PtX₆ (X = Cl, Br) salts
    
    Mendeleev Commun., 9:5 (1999),  171–173
60. A novel stereoselective and catalytic C–C coupling reaction: acetylene dimerization accompanied by addition of iodine to yield (E,E)-1,4-diiodobuta-1,3-diene in the Pt^IV–I^––I₂–MeOH system
    
    Mendeleev Commun., 7:4 (1997),  130–131
61. Silylformylation of Alkynes Catalysed by Di-μ-chlorotetrakis(η²-methylene-cyclopropane)dirhodium
    
    Mendeleev Commun., 5:6 (1995),  220–221
62. Phosphirenes and Diphosphetenes: the Products of the Reaction of λ³-lminophosphines with 1-Alkoxy- and 1-Aminoalkynes
    
    Mendeleev Commun., 3:2 (1993),  68–70
63. Di-μ-chlorotetrakis(η²-methylenecyclopropane)dirhodium. A Highly Active Catalyst for Hydrosilylation of Alkenes and Alkynes
    
    Mendeleev Commun., 2:4 (1992),  136–137
64. Synthesis of Aryl Esters by Pd-catalysed Carbonylation of Aryl Iodides
    
    Mendeleev Commun., 1:4 (1991),  129–131
65. Key steps in the cross-coupling of organometallic compounds with organic halides, catalysed by nickel and palladium compounds
    
    Usp. Khim., 59:12 (1990),  2003–2020
66. Introduction of a carbon–carbon bond into electron-deficient aromatic compounds
    
    Usp. Khim., 59:8 (1990),  1288–1337
67. Substitutional Carbonylation of Organic Compounds Catalysed by Palladium Complexes
    
    Usp. Khim., 57:4 (1988),  529–561
68. The Cleavage of the Carbon–Carbon Bond in Carbonyl Compounds and Alcohols under the Influence of Bases
    
    Usp. Khim., 56:10 (1987),  1717–1752
69. Reactions of Carbonyl Compounds with Organic Derivatives of Alkali Metals and Hydride Reductants: the Effects of the Medium and the Cation
    
    Usp. Khim., 56:5 (1987),  793–813
70. Oxidation of Organometallic Compounds by Transition Metal Salts
    
    Usp. Khim., 51:6 (1982),  881–924
71. Oxidation of AlkyI Derivatives of Aromatic Hydrocarbons by Transition Metal Salts
    
    Usp. Khim., 50:6 (1981),  1007–1045
72. Oxidative Decarboxylation of Carboxylic Acids
    
    Usp. Khim., 49:12 (1980),  2257–2285
73. A New Mechanism of Nucleophilic Substitution
    
    Usp. Khim., 48:5 (1979),  793–828
74. The Reactivity of Carbanions
    
    Usp. Khim., 47:5 (1978),  819–846
75. The Interaction of Organometallic Derivatives with Organic Halides
    
    Usp. Khim., 45:4 (1976),  661–694
76. Ions and Ion-pairs in Nucleophilic Aliphatic Substitution
    
    Usp. Khim., 44:12 (1975),  2205–2248
77. Equilibrium Acidity of Carbon–Hydrogen Bonds in Organic Compounds
    
    Usp. Khim., 43:1 (1974),  35–63
78. Protolysis of dibenzyl mercury according to the $S_E1$ mechanism
    
    Dokl. Akad. Nauk SSSR, 163:6 (1965),  1381–1384
79. Protolysis mechanism of cis- and trans-$\beta$-chlorovinylmercury chlorides when acted upon by $\mathrm{HCl}$ and $\mathrm{DCl}$
    
    Dokl. Akad. Nauk SSSR, 162:1 (1965),  86–89
80. The mechanism of electrophile and homolytic substitution in the olefine carbon atom
    
    Dokl. Akad. Nauk SSSR, 161:3 (1965),  586–589
81. The influence of the substituents in the electrofilic bimolecular reaction
    
    Dokl. Akad. Nauk SSSR, 155:5 (1964),  1095–1097
82. Unusual effect of substituents in $S_E$ 2-reaction
    
    Dokl. Akad. Nauk SSSR, 153:3 (1963),  588–591
83. The “cosymmetrization” reaction of organomercuric salts
    
    Dokl. Akad. Nauk SSSR, 149:1 (1963),  90–93
84. Electrophile substitution in an unsaturated carbon atom. The influence of the medium on the reaction mechanism in the case of isotopic exchange between the ethyl ether of $\alpha$-horhomercurophenylacetic acid and $\mathrm{Hg}^{203}$ labelled mercuric bromide
    
    Dokl. Akad. Nauk SSSR, 136:3 (1961),  631–633
85. The mechanism of bimolecular electrophilic substitution in a saturated carbon atom
    
    Dokl. Akad. Nauk SSSR, 131:4 (1960),  853–856
86. The kinetics of the electrophile substitution at a saturated carbon atom
    
    Dokl. Akad. Nauk SSSR, 116:4 (1957),  617–620