Demidov Oleg P

Publications in Math-Net.Ru

1. Synthetic protocol for the preparation of new ([2,2':6',2''-terpyridin]-4'-yl)naphthalene derivatives
   
   Mendeleev Commun., 35:1 (2025),  96–98
2. Crystal structure and properties of new benzimidazopyrido[2,3-b]indole-6-carbonitriles
   
   Mendeleev Commun., 34:2 (2024),  274–276
3. β-Carbolines as intermediates in indirect heteroarylation of tryptamines exemplified by the synthesis of 2-pyrazolyltryptamines
   
   Mendeleev Commun., 33:5 (2023),  645–647
4. New β-[o-(5-oxopyrazol-3-yl)aryl]ethylamines and their unusual metastable betaine form
   
   Mendeleev Commun., 33:2 (2023),  203–205
5. α-Amino acid-assisted autoxidation of naphthalene proton sponge affording 1,4-naphthoquinone nitrogen derivatives
   
   Mendeleev Commun., 33:2 (2023),  197–200
6. 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
7. Synthesis, molecular structure and biological activity of Niⁱⁱ complexes based on substituted 2-(2-hydroxyphenyl)benzoxazole
   
   Mendeleev Commun., 32:6 (2022),  763–765
8. Photo- and ionochromic properties of new spirobenzochromene-pyranoquinoline
   
   Mendeleev Commun., 32:4 (2022),  531–533
9. Unusual cyclization of N-imidazolyl quinone imines with the formation of thiadiazole ring and its subsequent recyclization
   
   Mendeleev Commun., 32:3 (2022),  386–389
10. 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
11. Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion
    
    Mendeleev Commun., 31:4 (2021),  545–547
12. Thiourea assisted recyclization of 1-(chloromethyl)dihydroisoquinolines: a convenient route to β-(o-thiazolylaryl)ethylamines
    
    Mendeleev Commun., 31:1 (2021),  125–127
13. 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