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Publications in Math-Net.Ru
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Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives
Mendeleev Commun., 29:5 (2019), 584–586
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Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines
Mendeleev Commun., 28:6 (2018), 584–586
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Syntheses of chiral nopinane-annelated pyridines of C2 and D2-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9’-bi-4,5-diazafluorenylidene
Mendeleev Commun., 27:2 (2017), 128–130
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Syntheses of α-cyano substituted oximes from terpenic hydrocarbons via nitroso chlorides: X-ray structures of 3-cyanocaran-4-one oxime, 2-cyanopinan-3-one oxime and 1-cyano-p-menth-8-en-2-one oxime
Mendeleev Commun., 25:2 (2015), 93–95
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Stereoselective functionalisation of pinopyridine with anisidines and o-phenylenediamine
Mendeleev Commun., 21:5 (2011), 253–255
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Efficient synthesis of β-hydroxy sulfides by microwave-promoted ring opening in (+)-3-carene trans-epoxide with sodium thiolates
Mendeleev Commun., 21:4 (2011), 192–193
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First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.04,16]hexadeca-1,12-diene
Mendeleev Commun., 19:5 (2009), 246–247
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Mannich-type three component condensation of α-substituted caran-4-one oximes with formaldehyde and secondary amines
Mendeleev Commun., 19:3 (2009), 139–140
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Chirospecific analysis of plant volatiles
Usp. Khim., 76:10 (2007), 1014–1033
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Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro- 6H-benzo[c]quinolizine using the tert-amino effect
Mendeleev Commun., 16:2 (2006), 82–83
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C-Alkylation of nitroso chlorides with diethyl malonate: the X-ray structure of diethyl (±)-(1R*,2S*,5R*)-2-{3(E)-hydroxyimino-2,6,6-trimethylbicyclo[3.1.1]-hept-2-yl}malonate
Mendeleev Commun., 14:1 (2004), 18–20
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Formation of an optically active 2-phenyl[1,2,4]triazolo[1,5-a]pyrimidine derivative in the reaction of (+)-3-carene-derived β-chlorovinylketone with benzylidene aminoguanidine
Mendeleev Commun., 12:6 (2002), 226–227
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Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime
Mendeleev Commun., 12:3 (2002), 88–89
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Transformation of myrtenoic acid nitrile to aminophospholene oxide by the reaction with dibenzylphosphine oxide: the X-ray structure of (1S*,2R*,6R*,8R*)-5-benzyl-9,9-dimethyl-5-oxo-4-phenyl- 5-phosphatricyclo[6.1.1.02,6]dec-3-en-3-ylamine
Mendeleev Commun., 11:3 (2001), 98–99
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New approach to [a]-fused fluoroquinolones: the synthesis of 5-oxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinolines
Mendeleev Commun., 11:2 (2001), 53–54
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N-Alkylation in the reactions of 5-imidazolylphenylthiourea with alkyl halides and chloroacetone
Mendeleev Commun., 10:6 (2000), 233–235
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Unusual acid-induced heterocyclisation of caryophyllene-type α-amino oximes: X-ray structure of (1S,2S,5R,8S)-1,4,4,8-tetramethyl-8-morpholin-4-yl-11-oxa-10-azatricyclo[7.2.2.02,5]tridec-9-ene
Mendeleev Commun., 10:6 (2000), 211–212
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Novel terpene-based chiral bis-α-aminooximes and the corresponding macrocycles: X-ray structure of a ring-fused 5,7-dioxa-1,4,8,11-tetraazacyclotrideca-3,8-diene derivative
Mendeleev Commun., 10:6 (2000), 209–210
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Nitrosochlorination of acyclic monoterpenoids
Mendeleev Commun., 10:4 (2000), 146–148
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Synthesis of chiral fused pyrimidines from (+)-3-carene- and limonene-derived isomeric β-enaminones
Mendeleev Commun., 10:3 (2000), 112–114
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Nitrosochlorination of cembrene
Mendeleev Commun., 10:3 (2000), 109–111
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A new ring transformation in the series of 1,2,3-thiadiazoles. Synthesis of 5H-[1,2,3]triazolo[5,1-b][1,3,4]thiadiazines
Mendeleev Commun., 10:1 (2000), 19–20
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Transformation of diaminocarane on a triosmium cluster. Absolute configuration of a cluster with a bridging imidyl ligand
Mendeleev Commun., 9:6 (1999), 213–214
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Synthesis of diethyl oxo phosphonates from monoterpene ketones – carvone, pinocarvone and 2-caren-4-one
Mendeleev Commun., 7:4 (1997), 141–143
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Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame
Mendeleev Commun., 7:4 (1997), 139–141
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Syntheses of novel chiral quinoxaline derivatives from seco-derivatives of monoterpene hydrocarbons 3-carene and α-pinene
Mendeleev Commun., 7:3 (1997), 114–115
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Synthesis of monoterpenic α-amino ketones
Mendeleev Commun., 6:2 (1996), 64–66
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New pyrazole-, isoxazole- and N-acylpyrazoline derivatives with a pinane carbon frame
Mendeleev Commun., 6:1 (1996), 18–20
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Synthesis of (–)-Caronaldehyde from ( + )-3-Carene
Mendeleev Commun., 5:5 (1995), 179–180
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Enaminones of the 2-Acetylcyclopent-1-en-1-ylamine Type Derived from the Terpenic Compounds Limonene, 3-Carene and δ-Cadinol
Mendeleev Commun., 2:4 (1992), 161–162
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An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime
Mendeleev Commun., 2:3 (1992), 82–83
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Is the Six-Membered Ring of the 3-Carene Molecule Planar?
Mendeleev Commun., 1:3 (1991), 98–99
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