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81
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Kravchenko A.N.
, Baranov V.V.
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, Chikunov I.E.
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Regioselective reactions of N-(carboxyalkyl)- and N-(aminoethyl)ureas with glyoxal and 1,2-dioxo-1,2-diphenylethane
Russian Chemical Bulletin. 2014.
V.63. N2. P.416-421. DOI: 10.1007/s11172-014-0446-5
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82
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Gazieva G.A.
, Kolotyrkina N.G.
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Synthesis of novel spiro[indole-3,3′-pyrrolidin]-2(1H)-ones
Russian Chemical Bulletin. 2014.
V.63. N2. P.431-434. DOI: 10.1007/s11172-014-0449-2
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83
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Gazieva G.A.
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Unexpected formation of 4-alkyl-5-(4-alkylthiosemicarbazido)-4,5-dihydro-1,2,4-triazine-3(2H)-thiones from 1,3-dialkyl-4,5-bis-(4-alkylthiosemicarbazido)imidazolidin-2-ones in acidic medium
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V.24. N1. P.42-44. DOI: 10.1016/j.mencom.2013.12.014
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84
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Gazieva G.A.
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Target synthesis of bioactive thioglycolurils, based on QSAR predictions
Mendeleev Communications. 2013.
V.23. N4. P.202-203. DOI: 10.1016/j.mencom.2013.07.007
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85
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Gazieva G.A.
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Synthesis of New Imidazo[4,5-e][1,3]thiazolo-[3,2-b][1,2,4]triazine Derivatives
Chemistry of Heterocyclic Compounds. 2013.
V.49. N7. P.1097-1101. DOI: 10.1007/s10593-013-1349-3
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86
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Gazieva G.A.
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Synthesis of imidazo[4,5-e][1,3]thiazolo-[3,2-b][1,2,4]triazines
Chemistry of Heterocyclic Compounds. 2012.
V.48. N9. P.1382-1389. DOI: 10.1007/s10593-012-1147-3
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87
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Gazieva G.
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, Popov L.
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A Novel Synthesis of Thioglycolurils by Ring Contraction of 5,7-Dialkyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-ones
Synthesis-Stuttgart. 2012.
V.44. N21. P.3366-3370. DOI: 10.1055/s-0032-1317194
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88
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Kravchenko A.N.
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[3 + 2]-Cycloaddition of azomethine ylide at 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones
Mendeleev Communications. 2012.
V.22. N2. P.90-91. DOI: 10.1016/j.mencom.2012.03.013
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89
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Kravchenko A.N.
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HNO2-Assisted Triazine Cycle Contraction in 3-oxo-,3-thioxo- and 3-imino-5,7-dimethyl-4a,7a-diphenyl-perhydroimidazo[4,5-e][1,2,4]triazin-6-ones
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V.22. N6. P.299-301. DOI: 10.1016/j.mencom.2012.11.006
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90
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Diastereoselective synthesis of 4,5-dihydroxyimidazolidin-2-ones (-thiones) and their structure
Russian Chemical Bulletin. 2012.
V.61. N1. P.64-73. DOI: 10.1007/s11172-012-0010-0
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91
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Baranov V.V.
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α-Thioureidoalkylation of functionally substituted ureas: I. Tandem cyclization and esterification in reactions of N-(carboxyalkyl)ureas with 1,3-dialkyl-4,5-dihydroxy-4,5-diphenylimidazolidine-2-thiones in alcohols
Russian Journal of Organic Chemistry. 2011.
V.47. N10. P.1564-1571. DOI: 10.1134/s1070428011100204
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V.47. N2. P.210-214. DOI: 10.1007/s10593-011-0742-z
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93
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Gazieva G.A.
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Russian Journal of Organic Chemistry. 2011.
V.47. N10. P.1572-1575. DOI: 10.1134/s1070428011100216
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94
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4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-aminoalkylureas 5. Synthesis of N-hydroxyalkyl-1,5-diphenylglycolurils
Russian Chemical Bulletin. 2010.
V.59. N6. P.1296-1299. DOI: 10.1007/s11172-010-0236-7
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95
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Condensation of 5,7-dimethyl-4a,7a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-one with halogenoacetic acids
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V.20. N1. P.47-49. DOI: 10.1016/j.mencom.2010.01.018
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96
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4,5-Dihydroxyimidazolidin-2-ones in α-ureidoalkylation of N-carboxyalkyl-, N-hydroxyalkyl-, and N-(aminoalkyl)ureas 4.* α-Ureidoalkylation of N-(2-acetylaminoethyl)ureas
Russian Chemical Bulletin. 2010.
V.59. N3. P.642-646. DOI: 10.1007/s11172-010-0117-0
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The synthesis, structure, and electron density distribution in crystals of 4,5-dihydroxyimidazolidine-2-thiones
Russian Chemical Bulletin. 2009.
V.58. N7. P.1353-1360. DOI: 10.1007/s11172-009-0181-5
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98
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Gazieva G.A.
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4,5-Dihydroxyimidazolidin-2-ones in an α-ureidoalkylation reaction of N-(carboxyalkyl)-, N-(hydroxyalkyl)-, and N-(aminoalkyl)ureas 3. α-Ureidoalkylation of N-[2-(dimethylamino)ethyl]urea
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V.58. N12. P.2488-2493. DOI: 10.1007/s11172-009-0348-0
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99
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α-Thioureidoalkylation of urea heteroanalogs
Russian Chemical Bulletin. 2009.
V.58. N9. P.1945-1954. DOI: 10.1007/s11172-009-0266-1
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100
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3,3′-bi(6,8-dialkyl-2,4-dioxa-7-thia-6,8-diazabicyclo[3.3.0]-octane-7,7-dioxides): Structure and synthesis
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V.45. N2. P.248-255. DOI: 10.1134/s107042800902016x
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