Морковник Анатолий Савельевич

Публикации в базе данных Math-Net.Ru

1. A new method for constructing pyrido[3',2':4,5]imidazo[1,2-b]pyridazine system and preparation of its derivatives
   
   Mendeleev Commun., 35:1 (2025),  24–26
2. β-Carbolines as intermediates in indirect heteroarylation of tryptamines exemplified by the synthesis of 2-pyrazolyltryptamines
   
   Mendeleev Commun., 33:5 (2023),  645–647
3. New β-[o-(5-oxopyrazol-3-yl)aryl]ethylamines and their unusual metastable betaine form
   
   Mendeleev Commun., 33:2 (2023),  203–205
4. Novel recyclization of 3,4-dihydroisoquinolines as an efficient route to a new type of heteroarylated derivatives of β-arylethylamines
   
   Mendeleev Commun., 32:6 (2022),  795–797
5. New type of recyclization in 3,4-dihydroisoquinolines in the synthesis of β-(o-indazolylaryl)ethylamines and their 7-azaindazolyl analogues
   
   Mendeleev Commun., 32:2 (2022),  265–267
6. Nitration of 2,3-dihydroimidazo[1,2-a]benzimidazole and its N 9-substituted derivatives
   
   Mendeleev Commun., 31:4 (2021),  555–557
7. Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion
   
   Mendeleev Commun., 31:4 (2021),  545–547
8. Thiourea assisted recyclization of 1-(chloromethyl)dihydroisoquinolines: a convenient route to β-(o-thiazolylaryl)ethylamines
   
   Mendeleev Commun., 31:1 (2021),  125–127
9. New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines
   
   Mendeleev Commun., 30:1 (2020),  28–30
10. 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
11. Uncommon condensations of 1,2,3-triketone 2-oximes with o-phenylenediamine
    
    Mendeleev Commun., 29:1 (2019),  111–113
12. 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
13. Novel reactions of ninhydrin oxime with mercaptoalkanoic acids
    
    Mendeleev Commun., 28:3 (2018),  300–302
14. 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
15. Recyclization of glaucine as a new route to litebamine derivatives
    
    Mendeleev Commun., 28:1 (2018),  58–60
16. Unexpected domino reaction of 3-alkyl-1,2,4-triazolo[1,5-a]benzimidazoles with butylmagnesium bromide leading to benzimidazolyl guanidines
    
    Mendeleev Commun., 26:4 (2016),  320–322
17. Synthesis of 6’ H-spiro(indene-2,2’ -[1,3]oxathiane)-1,3,5’ -triones
    
    Mendeleev Commun., 23:6 (2013),  352–353
18. Structure and tautomerism of 2-benzimidazolylthioureas
    
    Mendeleev Commun., 17:4 (2007),  224–226
19. Steric control in the ion radical nitration of 5-triphenylmethylbenzimidazolines using a silver/nitrite system
    
    Mendeleev Commun., 7:5 (1997),  175–176
20. A New Class of Benzoin Condensation Catalysts: N,N′-Disubstituted o-Phenylenediamines
    
    Mendeleev Commun., 5:1 (1995),  11–12
21. Окислительно-восстановительная стадия в реакции нитрования
    
    Усп. хим., 57:2 (1988),  254–280
22. Неорганические ион-радикалы и их органические реакции
    
    Усп. хим., 48:11 (1979),  1968–2006