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Публикации в базе данных Math-Net.Ru
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Synthesis of new heterocyclic systems fused at pyrazolo[3,4-c]-2,7-naphthyridine core
Mendeleev Commun., 32:3 (2022), 393–394
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Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion
Mendeleev Commun., 31:4 (2021), 545–547
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Thiourea assisted recyclization of 1-(chloromethyl)dihydroisoquinolines: a convenient route to β-(o-thiazolylaryl)ethylamines
Mendeleev Commun., 31:1 (2021), 125–127
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Nucleophilic substitution of hydrogen–the Boger reaction sequence as an approach towards 8-(pyridin-2-yl)coumarins
Mendeleev Commun., 29:3 (2019), 299–300
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The novel structural modification of pyridoxal via its cyclization into 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines
Mendeleev Commun., 29:1 (2019), 116–118
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Synthesis of phenanthro[1,2-d]azepine derivatives containing a new heterocyclic system from the aporphine alkaloid glaucine
Mendeleev Commun., 28:3 (2018), 320–322
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Reaction of 2-methyl-3,4-dihydro-β-carbolin-2-ium iodide with acylmethyl halides controlled by electronic effects: a new route to 1,2-dihydroazepino[4,5-b]indoles
Mendeleev Commun., 28:1 (2018), 83–85
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Recyclization of glaucine as a new route to litebamine derivatives
Mendeleev Commun., 28:1 (2018), 58–60
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Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-ols and guanidine
Mendeleev Commun., 22:2 (2012), 114–116
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Stereochemical outcome of the T-reaction employing chiral bicyclic amines
Mendeleev Commun., 17:6 (2007), 318–320
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Interaction of barbituric acids with o-dialkylaminobenzaldehydes
Mendeleev Commun., 16:1 (2006), 52–54
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Механизм направляющего влияния функциональных групп и геометрии молекул реагентов на пероксидное эпоксидирование алкенов
Усп. хим., 68:3 (1999), 206–226
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Inter-ring Long-range Spin-Spin Proton Coupling in some 8-Hydroxyquinoline Derivatives
Mendeleev Commun., 3:3 (1993), 107–108
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New Rearrangement in the o-Methoxycarbonyl-ω-diazoacetophenone Series
Mendeleev Commun., 2:1 (1992), 8–10
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Новые направления в создании пестицидов с низкой экологической нагрузкой
Усп. хим., 60:3 (1991), 553–554
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