The influence of the structure of 4-oxoalkan-1,1,2,2-tetrakarbonitrila the direction their interaction with secondary amines, as the result developed new methods for the synthesis of various 3,3-substituted 3H-pyrroles.
3Н-пирролы, 4-оксоалкан-1,1,2,2-тетракарбонитрилы, β-цианогруппы, γ-цианогруппы, 3H-pyrroles, 4-оxoalkane-1,1,2,2-tetracarbonitriles,, β-cyano groups, γ-cyano groups
1. Padmavathi, V. Synthesis and Biological Activity of a New Class of Sulfone-Linked Pyrrolylpyrazoles and Pyrrolylisoxazoles from Methyl-3-aryl-2-(E-arylethenesulfonyl)acrylate / V. Padmavathi, L.T Radha, K. Mahesh, A.A. Padmaja // Chem. Pharm. Bull. - 2009. - Vol. 57. - № 11. - P. 1200-1205.
2. Muratake, H. Synthesis of Duocarmycin SA by Way of Methyl 4-(Methoxycarbonyl)oxy-3H-pyrrolo[3, 2-f]quinoline-2-carboxylate as a Tricyclic Heteroaromatic Intermediate / H. Muratake, M. Tonegawa, M. Natsume // Chem. Pharm. Bull. - 1998. - Vol. 46. - № 3. - P. 400-412.
3. Belikov, M.Yu. Reaction between 4-oxoalkane-1,1,2,2-tetracarbonitriles and morpholine: regioselective synthesis of -amino-2-(morpholin-4-yl)-3-(2-oxoalkyl)-3H-pyrrol-3,4-dicarbonitriles / M.Yu. Belikov, O.V. Ershov, A.V. Eremkin, O.E. Nasakin, V.A. Tafeenko, E.V. Nurieva // Tetrahedron Letters. - 2011. - № 52. - R. 6407-6410.
4. Belikov, M.Yu. Sintez -amino-3H-pirrol-3,4-dikarbonitrilov na osnove tetracianoetilirovannyh zhirnoaromaticheskih ketonov / M.Yu. Belikov, O.V. Ershov, I.V. Lipovskaya, A.V. Eremkin, O.E. Nasakin // ZhOrH. - 2011. - T.47. - №9. - S. 1401-1402.
5. Belikov, M.Yu. Vzaimodeystvie 4-oksoalkan-1,1,2,2-tetrakarbonitrilov s ammiakom i aminami / M.Yu. Belikov // Avtoref. dis. kand. him. nauk. - Kazan'. - 2011. - 23 s.
6. Nasakin, O.E. The Synthesis of 3-Amidinio-2-amino-pyridine-4-Carboxylates / O.E. Nasakin, V.P. Sheverdov, I.V. Moiseeva, A.N. Lyshchikov, O.V. Ershov, V.N. Nesterov // Tetrahedron Letters. - 1997. - Vol.- № 25. - P. 4455-4456.
7. Belikov, M.Yu., Poluchenie 3,4-diciano-5,6,7,8-tetragidrohinolin-2-olyatov dietilammoniya / M.Yu. Belikov, O.V. Ershov, A.V. Eremkin, Ya.S. Kayukov, O.E. Nasakin // ZhOrH. - 2010. - T. 46. № 4.- S.621-622.
8. Lipin, K.V. Trehkomponentnyy sintez i biologicheskaya aktivnost' 2-hloropiridin-3,4-dikarbonitrilov / K.V. Lipin, V.N. Maksimova, O.V. Ershov, O.E. Nasakin, L.F. Sattarova, B.P. Strunin, V.A. Antipov, P.A. Gurevich // Vestnik Kazanskogo tehnol. un-ta. - 2010. - № 8. - S. 37-40.
9. Gurevich, P.A. Sintez i biologicheskaya aktivnost' -galogen-5,6,7,8-tetragidrohinolin-3,4-dikarbonitrilov / P.A. Gurevich, V.N. Maksimova, K.V. Lipin, O.V. Ershov, O.E. Nasakin, L.F. Sattarova, N.G. Mogil'nyy, B.P. Strunin // Vestnik Kazanskogo tehnol. un-ta. - 2012. - № 1. - S. 90-93.
10. Belikov, M.Yu. Sintez pirrolo[3,4-c]pirrolov i hinolin-3,4-dikarbonitrilov na osnove -oksoalkan-1,1,2,2-tetrakarbonitrilov / M.Yu. Belikov, O.V. Ershov, I.V. Lipovskaya, O.E. Nasakin, B.P. Strunin, V.A. Antipov, L.F. Sattarova, P.A. Gurevich // Vestnik Kazanskogo tehnol. un-ta. - 2010. - № 9. - S. 112-115.
11. Belikov, M.Yu., Poluchenie novogo organicheskogo aniona vzaimodeystviem -aril(geteril)-4-oksobutan-1,1,2,2-tetrakarbonitrilov s ammiakom / M.Yu. Belikov, O.V. Ershov, A.V. Eremkin, Ya.S. Kayukov, O.E. Nasakin // ZhOrH. - 2010. - T. 46. № 4. - S. 604-605.
12. Belikov, M.Yu. Sintez i biologicheskaya aktivnost' produktov vzaimodeystviya -oksoalkan-1,1,2,2-tetrakarbonitrilov s aminami / M.Yu. Belikov, O.V. Ershov, O.E. Nasakin, B.P. Strunin, V.A. Antipov, L.F. Sattarova, P.A. Gurevich // Vestnik Kazanskogo tehnol. un-ta. - 2010. - № 8. - S. 28-31.
13. Nasakin, O.E. Single-stage synthesis of -amino-1,2-dicyano-4,6-diazabibicyclo[3.2.1]oct-2-en-7-ones from b,b,g,g-tetracyanoalkanones / O.E. Nasakin, V.P. Sheverdov, O.V. Ershov, I.V. Moiseeva, A.N. Lyshchikov, V.N. Khrustalev, M.Yu. Antipin // Mendeleev Communications. - 1997. - Vol. 7. - № 3. - P.112-113.
14. Ducker, J.M. The reaction of ethentetracarbonitrile with acyclic b-dicarbonyl compounds and related studies / J.M. Ducker, M.J. Gunter // Australian Journal Chemistry. - 1973. - Vol. 26. - № 7. - P. 1551-1569.
