Абрамов Игорь Геннадьевич

Публикации в базе данных Math-Net.Ru

1. Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles
   
   Mendeleev Commun., 28:1 (2018),  86–87
2. The C-3 chlorination of 2-aryl-1-hydroxyindoles
   
   Mendeleev Commun., 27:5 (2017),  498–499
3. Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles
   
   Mendeleev Commun., 25:4 (2015),  315–317
4. Synthesis of 7,8-dicyanopyrimido[2,1-b][1,3]benzothiazoles
   
   Mendeleev Commun., 23:4 (2013),  215–216
5. Synthesis of 2-oxo- and 2-thioxo-5-(benzofuran-2-yl)tetrahydropyrimidines
   
   Mendeleev Commun., 21:1 (2011),  46–47
6. Synthesis of 5,6-dicyanobenzofurans based on 4-bromo-5-nitrophthalonitrile
   
   Mendeleev Commun., 19:6 (2009),  332–333
7. Synthesis of expanded alkylphenoxythiadiazole macroheterocycles
   
   Mendeleev Commun., 18:5 (2008),  289–290
8. Synthesis of substituted azines with the participation of 4-bromo-5-nitrophthalonitrile
   
   Mendeleev Commun., 12:3 (2002),  120–121
9. 4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions
   
   Mendeleev Commun., 12:2 (2002),  72–74
10. Synthesis of oxygen-containing heterocyclic ortho-dinitriles based on 4-bromo-5-nitrophthalonitrile
    
    Mendeleev Commun., 11:2 (2001),  80–81
11. The differing reactivity of the bromo and nitro groups in 4-bromo-5-nitrophthalonitrile towards nucleophilic attack
    
    Mendeleev Commun., 10:2 (2000),  78–80
12. Selective Hydrogenolysis of the C–F Bond
    
    Mendeleev Commun., 1:4 (1991),  118–119