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Kostyanovsky Remir Grigorevich

Publications in Math-Net.Ru

  1. 1-Alkoxyamino-4-dimethylaminopyridinium salts: synthesis and structure†

    Mendeleev Commun., 26:2 (2016),  169–171
  2. Synthesis and structure of N-alkoxyhydrazines and N-alkoxy-N’,N’,N’-trialkylhydrazinium salts

    Mendeleev Commun., 23:5 (2013),  289–291
  3. Molecular Structure of N-azidomethyl-N,N-dimethylamine According to Gas-phase Electron Diffraction Data and Quantum-chemical Calculations

    Mendeleev Commun., 23:3 (2013),  166–167
  4. The properties and structure of N-chloro-N-methoxy-4-nitrobenzamide

    Mendeleev Commun., 22:3 (2012),  164–166
  5. 1-Alkoxyamino-4-dimethylaminopyridinium derivatives as new representatives of O–N–N+ geminal systems and their structure†

    Mendeleev Commun., 22:2 (2012),  92–94
  6. N,3-Dimethyl-3-(perhydro-1,3,2-dioxazepin-2-yl)butanamide: synthesis and crystal structure

    Mendeleev Commun., 21:6 (2011),  349–350
  7. 1-Hydroxy-8-methyl-1,4,8-triazaspiro[4.5]decan-2-one and its (±)-3-methyl homologue: regioselective synthesis and in vivo evaluation as adjuvants in leukemia chemotherapy

    Mendeleev Commun., 21:5 (2011),  239–241
  8. New approach to N,N-dialkoxy-N′-arylureas and N,N-dialkoxycarbamates

    Mendeleev Commun., 21:1 (2011),  50–52
  9. Simple chiral auxiliary-assisted resolution of 2-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid

    Mendeleev Commun., 20:5 (2010),  291–292
  10. Pyramidal nitrogen in the crystal of N-[(benzoyl)-(hydroxy)methyl]-N-benzyloxy-N’-(2-bromophenyl)urea

    Mendeleev Commun., 20:3 (2010),  167–169
  11. General regioselective synthesis and crystal structure of racemic 5-substituted 2,2-dimethyl-3-hydroxyimidazolidin-4-ones

    Mendeleev Commun., 20:2 (2010),  106–108
  12. Cyanomethylamines and azidomethylamines: new general methods of the synthesis and transformations

    Mendeleev Commun., 19:5 (2009),  281–283
  13. Reaction of diaziridine-3,3-dicarboxylic acid dihydrazide with acetone

    Mendeleev Commun., 19:2 (2009),  81–83
  14. Isomorphism of chiral ammonium salts Ph(All)N+Et(Me)X–·CHCl3

    Mendeleev Commun., 19:1 (2009),  19–20
  15. The enigma of a (±)-tartaric acid–urea cocrystal

    Mendeleev Commun., 19:1 (2009),  17–18
  16. Synthesis and crystal structure of new imidazolidine-2,4-dione and imidazolidin-2-one derivatives

    Mendeleev Commun., 18:2 (2008),  102–104
  17. Absolute configuration of a chiral proton sponge

    Mendeleev Commun., 18:2 (2008),  86–87
  18. ClO3–···ClO3 – interactions in crystalline sodium chlorate

    Mendeleev Commun., 18:1 (2008),  29–31
  19. Spontaneous resolution of a chiral proton sponge

    Mendeleev Commun., 17:4 (2007),  214–215
  20. Synthesis, structure and properties of N-alkoxy-N-(1-pyridinium)urea salts, N-alkoxy-N-acyloxyureas and N,N-dialkoxyureas

    Mendeleev Commun., 17:3 (2007),  178–180
  21. N-Chloro-N-alkoxyureas: synthesis, structure and properties

    Mendeleev Commun., 16:6 (2006),  323–325
  22. Pyramidal amide nitrogen in N-acyloxy-N-alkoxyureas and N-acyloxy-N-alkoxycarbamates

    Mendeleev Commun., 16:4 (2006),  222–223
  23. The first conglomerate in fluorinated asymmetric nitrogen compounds

    Mendeleev Commun., 16:3 (2006),  139–141
  24. Sterically hindered fluorinated and brominated Tröger bases: synthesis and X-ray diffraction analysis

    Mendeleev Commun., 16:3 (2006),  138–139
  25. N,N-Dimethoxy-N-tert-alkylamines: new synthesis methods and the crystal structure of the precursor

    Mendeleev Commun., 16:2 (2006),  84–85
  26. Intermolecular N3···N3 interactions in the crystal of pentaerythrityl tetraazide

    Mendeleev Commun., 15:6 (2005),  232–234
  27. Methanetriacetic and methylmethanetriacetic acids, their precursors and derivatives: NMR and X-ray diffraction studies

    Mendeleev Commun., 15:5 (2005),  187–189
  28. Chirality-directed organogel formation

    Mendeleev Commun., 15:4 (2005),  140–141
  29. ESR study of stereochemistry in chiral nitroxide radical crystals

    Mendeleev Commun., 14:6 (2004),  318–320
  30. Stereochemistry of 1,2,4,5-tetraazanorbornanes and diaziridines: exciting history and news

    Mendeleev Commun., 14:6 (2004),  315–318
  31. Crystal engineering strategies in alkane-bis(ammonium) 2,5-diaza-3,6-dioxobicyclo[2.2.2]octane-1,4-dicarboxylates

    Mendeleev Commun., 14:6 (2004),  312–314
  32. Resolution and racemization of nonbenzenoid atropenantiomers

    Mendeleev Commun., 14:6 (2004),  310–312
  33. Stereochemisty of 3,3-disubstituted 2-methoxy-1,2-oxazolidines

    Mendeleev Commun., 14:6 (2004),  306–309
  34. Impossible things in stereochemistry

    Mendeleev Commun., 14:6 (2004),  229–230
  35. Acyloxy group exchange in N-acyloxy-N-alkoxyamides

    Mendeleev Commun., 14:5 (2004),  208–210
  36. One-step synthesis and structure of a tricyclic trislactone with C3 symmetry

    Mendeleev Commun., 14:3 (2004),  89–90
  37. Configurationally stable axially chiral N,N’-dialkyl-2,2’-biphenylene-N,N’-ureas

    Mendeleev Commun., 13:6 (2003),  275–276
  38. Chiral aziridine-trans-2,3-dicarboxylic acid derivatives: exciting history, re-examination and structures

    Mendeleev Commun., 13:5 (2003),  223–226
  39. Nitrogen chirality via the sterical veto of N inversion

    Mendeleev Commun., 13:3 (2003),  136–139
  40. 2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization

    Mendeleev Commun., 13:3 (2003),  116–118
  41. Spontaneous resolution in the imidazolidin-2-one series

    Mendeleev Commun., 13:3 (2003),  114–116
  42. Asymmetric three-coordinated nitrogen compounds: spontaneous resolution and absolute asymmetric synthesis

    Mendeleev Commun., 13:3 (2003),  111–113
  43. A new conglomerate in a series of 2,3:6,7-dibenzobicyclo[3.3.1]nonanes

    Mendeleev Commun., 13:3 (2003),  106–108
  44. Pasteur-like resolution of quasi-racemates in solid and gas phases

    Mendeleev Commun., 13:3 (2003),  97–99
  45. Louis Pasteur did it for us especially

    Mendeleev Commun., 13:3 (2003),  85–90
  46. Ångström-sized pore crystal

    Mendeleev Commun., 12:6 (2002),  220–222
  47. General regioselective synthesis of 2,2-disubstituted 3-hydroxyimidazolidin-4-ones

    Mendeleev Commun., 12:5 (2002),  193–196
  48. Sterically hindered nitrogen inversion in five-membered cyclic hydrazines

    Mendeleev Commun., 12:5 (2002),  189–193
  49. (±)-trans-1,2-Diaminocyclohexane crystallises as a conglomerate

    Mendeleev Commun., 12:4 (2002),  147–149
  50. Chiral 1-alkoxyaziridines: resolution, nitrogen inversion, stucture and diastereomeric transformations

    Mendeleev Commun., 12:4 (2002),  137–140
  51. 3-Hydroxy-2,2-dimethylimidazolidin-4-one: the regioselective synthesis and chiral crystallization

    Mendeleev Commun., 12:3 (2002),  85–87
  52. Chiral drugs via the spontaneous resolution

    Mendeleev Commun., 12:1 (2002),  6–8
  53. Directed synthesis of compounds capable to spontaneous resolution

    Mendeleev Commun., 12:1 (2002),  4–6
  54. Outer-sphere association of hexacyanoferrate and nitrogen betaine anions

    Mendeleev Commun., 11:5 (2001),  181–182
  55. Bis-aziridinomethanes: synthesis, structure and properties

    Mendeleev Commun., 11:4 (2001),  141–143
  56. Crystal properties of N-alkyl-substituted glycolurils as the precursors of chiral drugs

    Mendeleev Commun., 11:4 (2001),  134–136
  57. X-ray diffraction study of DL-1,4-dimethyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione: the sense of twist and folding

    Mendeleev Commun., 11:2 (2001),  49–50
  58. Stereoregular self-assembling of diastereomeric bicyclic bis-lactam diesters

    Mendeleev Commun., 11:1 (2001),  6–8
  59. Wedekind–Fock–Havinga salt Me(Et)N+(All)PhI–·CHCl3 as historically the first object for absolute asymmetric synthesis: spontaneous resolution, structure and absolute configuration

    Mendeleev Commun., 11:1 (2001),  1–5
  60. Molecular structure of 1-methoxymethylaziridine and methoxymethyldimethylamine and anomeric effects

    Mendeleev Commun., 10:6 (2000),  217–220
  61. Chirality-directed self-assembling of long-chain dialkyl 3,7-diazabicyclo[3.3.1]nonane-2,6-dione-1,5-dicarboxylates

    Mendeleev Commun., 10:3 (2000),  106–108
  62. Molecular structure of tris(aziridino)methane in the gas phase and crystalline state

    Mendeleev Commun., 10:3 (2000),  103–106
  63. Resolution of racemates with achiral reagents

    Mendeleev Commun., 10:3 (2000),  83–84
  64. Homochiral and pseudoracemic 3,3- and 1,2-dimethyldiaziridine–silver nitrate complexes

    Mendeleev Commun., 10:2 (2000),  44–46
  65. Spontaneous resolution of new conglomerates in the series of 4-arenesulfonyliminocyclohex-2-en-1-ones

    Mendeleev Commun., 10:1 (2000),  16–18
  66. 1,4-Dimethyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione: optical resolution, absolute configuration and circular dichroism

    Mendeleev Commun., 9:6 (1999),  229–231
  67. Chirality-directed co-crystallization of different configurationally opposite dialkyl 2,5-diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylates

    Mendeleev Commun., 9:4 (1999),  154–156
  68. 3,7-Dimethyl-3,7-diazabicyclo[3.3.1]nonane-2,6-dione-1,5-dicarboxylic acid derivatives: synthesis, structure and resolution

    Mendeleev Commun., 9:4 (1999),  151–154
  69. 2,5-Diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylic acids: synthesis, resolution, absolute configuration and crystal structures of the racemic and (–)-enantiomeric forms

    Mendeleev Commun., 9:3 (1999),  109–111
  70. 3,7-Diazabicyclo[3.3.1]nonane-2,6-diones: building of homo- and heterochiral crystals

    Mendeleev Commun., 9:3 (1999),  106–108
  71. 3,7-Diazabicyclo[3.3.0]octane-2,6-diones: synthesis, NMR spectra and structures

    Mendeleev Commun., 9:2 (1999),  70–73
  72. Optically active 2,2-dimethyl-1,3,4-triazabicyclo[4.1.0]heptan-5-one: synthesis, spontaneous resolution and absolute configuration

    Mendeleev Commun., 9:1 (1999),  26–27
  73. Chiral glycouril, 2,6-diethyl-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione: spontaneous resolution, reactivity and absolute configuration

    Mendeleev Commun., 8:6 (1998),  231–233
  74. α,α’-Diamino-α,α’-dicarboxyadipic acid tetraester: synthesis, lactamisation and dilactam structure

    Mendeleev Commun., 8:6 (1998),  228–230
  75. Sterically controlled population of the 1,2-cis-form of 1,2-dimethyl-3-tert-butyldiaziridine

    Mendeleev Commun., 8:3 (1998),  113–116
  76. N-Fluorination of aziridinecarboxylates via fluorolysis of their N-aminomethyl derivatives

    Mendeleev Commun., 8:2 (1998),  66–67
  77. Stereospecific synthesis of bicyclic diaziridines: 4a-chloro-; 4e,6a- and 4a,6e-dichloro-5-methoxycarbonyl-1,6-diazabicyclo[3.1.0]hexanes

    Mendeleev Commun., 8:2 (1998),  54–56
  78. Geminal oxygen–nitrogen–halogen systems. N-Halohydroxylamine derivatives

    Usp. Khim., 67:3 (1998),  203–218
  79. Methyl 2-trifluoromethylaziridine-2-carboxylate: stereodirected N-halogenation from the sterically more hindered side

    Mendeleev Commun., 7:6 (1997),  229–230
  80. Stereocontrolled synthesis and cyclization of (+,−)-α,α’-dihydroxy-α,α ’, β-trimethylglutaric acid derivatives

    Mendeleev Commun., 7:2 (1997),  64–66
  81. Unusual reaction of aziridine dimer with acetylene dicarboxylates

    Mendeleev Commun., 7:2 (1997),  56–58
  82. Derivatives of 1-fluoroaziridine-2,2-dicarboxylic acid

    Mendeleev Commun., 7:2 (1997),  54–55
  83. Autoassembling of the quinuclidine nucleus: one-step synthesis, structure and properties of dimethyl 4-hydroxy-6,6,7,7-tetramethyl-Δ2-dehydroquinuclidine-2,3-di-carboxylate

    Mendeleev Commun., 6:4 (1996),  143–145
  84. Heterolytic fragmentation of 4-hydroxy-6,6,7,7-tetramethyl-Δ2-dehydro-quinuclidine-2,3-dicarboxylic acid esters

    Mendeleev Commun., 6:3 (1996),  108–110
  85. 1,2-Di-tert-butyldiaziridine

    Mendeleev Commun., 6:3 (1996),  106–107
  86. 3,4-Di-tert-butyl-l,3,4-oxadiazolidine: synthesis and structure

    Mendeleev Commun., 6:2 (1996),  69–71
  87. A Novel trans-1,2-Dimethyldiaziridine–Silver Nitrate Complex: Synthesis and Molecular and Crystal Structure

    Mendeleev Commun., 5:6 (1995),  218–219
  88. A Superstable Nitrogen Pyramid: Stereodirected N-Halogenation of Methyl 2-Aziridinecarboxylate

    Mendeleev Commun., 5:6 (1995),  216–217
  89. Absolute Configuration of 1,4-Dialkyl-2,5-dioxabicyclo[2.2.1]heptane-3,6-dione Enantiomers

    Mendeleev Commun., 4:3 (1994),  97–99
  90. Stereochemistry of the Mannich Reaction, Illustrated by the Aminomethylation of Diaziridine

    Mendeleev Commun., 3:5 (1993),  212–213
  91. New Scope and Limitations in the Knorr–Paal Synthesis of Pyrroles

    Mendeleev Commun., 3:1 (1993),  21–23
  92. The Absolute Configuration of Pyrazidole

    Mendeleev Commun., 2:4 (1992),  130–131
  93. Synthesis and Properties of 2,3-Dimethoxy-1,4,2,3-dioxadiazinane and Dialkoxydiazene Oxides

    Mendeleev Commun., 2:2 (1992),  50–51
  94. Is there Ring–Chain Tautomerism in γ-Nitrosoalkanols?

    Mendeleev Commun., 1:1 (1991),  9–10
  95. The structure of the amide group in $n$-bromobenzoylethylenimine

    Dokl. Akad. Nauk SSSR, 175:3 (1967),  586–589
  96. Three-member cycles with coordination bond

    Dokl. Akad. Nauk SSSR, 164:5 (1965),  1054–1057
  97. Alkylidene-bis-ethylenimines

    Dokl. Akad. Nauk SSSR, 159:1 (1964),  142–145
  98. The structure and dual reactivity of $\mathrm{N}$-ethyleneminocarbinols

    Dokl. Akad. Nauk SSSR, 148:4 (1963),  839–842
  99. Gammet constants of the ethylenimine cycle

    Dokl. Akad. Nauk SSSR, 147:4 (1962),  843–845
  100. Reaction of ethylenimine with carbonyl compounds

    Dokl. Akad. Nauk SSSR, 139:4 (1961),  877–879
  101. Reaction of ethylenimine with formaldehyde

    Dokl. Akad. Nauk SSSR, 135:4 (1960),  853–856

© Steklov Math. Inst. of RAS, 2026