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Публикации в базе данных Math-Net.Ru
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Design and synthesis of pyrazolo[3,4-d]pyridazine 5,6-dioxides as novel NO-donors
Mendeleev Commun., 31:1 (2021), 42–45
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Synthesis of new pharmacologically oriented heterocyclic ensembles, [2-(1H-pyrazol-1-yl)thiazol-4-yl]furoxans
Mendeleev Commun., 29:3 (2019), 288–291
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Regioselective synthesis, structural diversification and cytotoxic activity of (thiazol-4-yl)furoxans
Mendeleev Commun., 28:6 (2018), 623–625
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Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes
Mendeleev Commun., 25:4 (2015), 257–259
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Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids
Mendeleev Commun., 25:2 (2015), 126–128
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Nucleophilic aromatic cine-substitution of hydrogen: the ionic liquid-promoted von Richter reaction
Mendeleev Commun., 25:1 (2015), 41–43
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Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans
Mendeleev Commun., 25:1 (2015), 36–38
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Успехи химии моноциклических амино- и нитрофуроксанов
Усп. хим., 82:11 (2013), 1007–1033
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Ionic Liquids-assisted Synthesis of 3,4-Dihydroisoquinolines by the Bishler–Napieralski Reaction
Mendeleev Commun., 22:5 (2012), 267–269
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Ionic liquid-assisted synthesis of 5-monoand 1,5-disubstituted tetrazoles
Mendeleev Commun., 21:6 (2011), 334–336
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Synthesis of 5-alkyl-2-amino-1,3,4-thiadiazoles and α,ω-bis(2-amino-1,3,4-thiadiazol-5-yl)alkanes in ionic liquids
Mendeleev Commun., 21:6 (2011), 331–333
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Henry and Mannich reactions of polynitroalkanes in ionic liquids
Mendeleev Commun., 21:1 (2011), 21–23
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The first example of the Schmidt reaction in ionic liquids
Mendeleev Commun., 20:6 (2010), 335–336
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Thermally induced rearrangement of the arylhydrazones of furoxan-3-yl carbonyl compounds
Mendeleev Commun., 16:5 (2006), 259–262
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Thermal rearrangements of 3-substituted 4-(3-ethoxycarbonylthioureido)-1,2,5-oxadiazole 2-oxides
Mendeleev Commun., 13:4 (2003), 188–190
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The base-induced cascade rearrangement of 4-acetylamino-3-arylazo-1,2,5-oxadiazole 2-oxides (furoxans) into 4-acetylamino-2-aryl-5-nitro-2H-1,2,3-triazoles
Mendeleev Commun., 11:6 (2001), 230–232
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