Батог Людмила Валентиновна

Публикации в базе данных Math-Net.Ru

1. Synthesis of 1,2,4-oxadiazole-, pyrrole- and 1,2,3-triazole-substituted (1,2,3-triazol-1-yl)furazans
   
   Mendeleev Commun., 18:3 (2008),  161–163
2. Synthesis and Dimroth rearrangement of 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles
   
   Mendeleev Commun., 14:2 (2004),  76–77
3. Azido-1,2,5-oxadiazoles in reactions with 1,3-dicarbonyl compounds
   
   Mendeleev Commun., 12:4 (2002),  159–162
4. Synthesis of 1-aryl(hetaryl)-1,2,3-triazoles with the use of ionic liquids
   
   Mendeleev Commun., 12:3 (2002),  83–84
5. First representatives of macrocyclic poly(diazene oxide furazans): 3,4:7,8:11,12:15,16-tetrafurazano-1,2,5,6,9,10,13,14-octaazacyclohexadeca-1,3,5,7,9,11,13,15-octaene 1,9- and 1,10-dioxides; 1,5,9,13-tetraoxide and its crystal structure
   
   Mendeleev Commun., 7:1 (1997),  5–7
6. Hypohalites as reagents for the macrocyclization of diamines of the furazan series
   
   Mendeleev Commun., 6:5 (1996),  193–195
7. Polydiazenofurazans: novel macrocyclic systems
   
   Mendeleev Commun., 6:2 (1996),  66–67
8. New Macrocyclic Systems – Tetrafurazano[3,4-c:3,4-e:3,4-i:3,4-k]-1,2,7,8-tetraazacyclododeca-1,3,5,7,9,11-hexane and Hexafurazano-[3,4-c:3,4-e:3,4-i:3,4-k:3,4-o:3,4-r]-1,2,7,8,13,14-hexaazacyclooctadeca-1,3,5,7,9,11,13,15,17-nonane by Oxidative Macrocyclization of Diaminodifurazanyl
   
   Mendeleev Commun., 4:3 (1994),  102