Iminocoumarins are a group of chemicals consisting of a coumarin with an attached imine group.

Many derivatives of 2-iminocoumarin are applied as luminescence indicators,[1] laser dyes,[2][3][4] also they are known as biologically active compounds.[5][6][7] Furthermore, structural features of 2-iminopyrane cycle cause unusual reactivity of these compounds.[8][9] Most of the reported transformations affect directly the iminopyrane cycle, and the iminogroup is the main target for nucleophilic and electrophilic attacks in many cases. However furthermore the iminogroup these compounds can contain other functional groups, which can participate in such interactions. Thus, vicinal arrangement of the imino and amide nucleophilic groups in 2-iminocoumarin-3-(thio)carboxoamides 4, 5 produces great opportunity to utilize these compounds as building blocks to construct different heterocyclic systems.

Iminocoumarins can be formed by a variation of the Knoevenagel condensation by reaction of salicylaldehyde with substituted acetonitriles.[10]

References

  1. ↑ Nikolov, P.; Tyutyulkov, N.; Dryanska, V. Zeitschrift für Naturforschung. 1987, 42 (9), 987-993
  2. ↑ Asimov, M.M.; Nikitchenko, V.M.; Novikov, A.I.; Rubinov, A.N.; Bor, Zs.; Gaty, L. (1988). "New high-efficiency biscoumarin laser dyes". Chemical Physics Letters. Elsevier BV. 149 (2): 140–144. doi:10.1016/0009-2614(88)87210-5. ISSN 0009-2614.
  3. ↑ Liepouri, F.; Foukaraki, E.; Deligeorgiev, T.G.; Katerinopoulos, H.E. (2001). "Iminocoumarin-based low affinity fluorescent Ca2+ indicators excited with visible light". Cell Calcium. Elsevier BV. 30 (5): 331–335. doi:10.1054/ceca.2001.0240. ISSN 0143-4160.
  4. ↑ Krimova A. I.; Petuchov V. A.; Popov M.B. Quant. Electronica (Moscow) 1985, 12 (10), 2163-2166
  5. ↑ Bylov, Igor E; Vasylyev, Maksym V; Bilokin, Yaroslav V (1999). "Synthesis and anti-inflammatory activity of N-substituted 2-oxo-2H-1-benzopyran-3-carboxamides and their 2-iminoanalogues". European Journal of Medicinal Chemistry. Elsevier BV. 34 (11): 997–1001. doi:10.1016/s0223-5234(99)00119-1. ISSN 0223-5234.
  6. ↑ Huang, Chi-Kuang; Wu, Feng-Ying; Ai, You-Xi (1995). "Polyhydroxylated 3-(N-phenyl) carbamoyl-2-iminochromene derivatives as potent inhibitors of tyrosine kinase p60c-src". Bioorganic & Medicinal Chemistry Letters. Elsevier BV. 5 (20): 2423–2428. doi:10.1016/0960-894x(95)00422-p. ISSN 0960-894X.
  7. ↑ Hadfield, J. A.; Pavlidis, V. H.; Perry, P. J.; McGown, A. T. Anti-Cancer Drugs. 1999, 10 (6), 591-595
  8. ↑ Zhuravel', Irina O.; Kovalenko, Sergiy M.; Ivachtchenko, Alexandre V.; Chernykh, Valentin P.; Shinkarenko, Pavlo E. (2004). "Synthesis of substituted 3-(5-amino-[1,3,4]thiadiazol-2-yl)-2H-pyrano[2,3-c]pyridin-2-ones". Journal of Heterocyclic Chemistry. Wiley. 41 (4): 517–524. doi:10.1002/jhet.5570410407. ISSN 0022-152X.
  9. ↑ O'Callaghan C.N. Proc. R. Ir. Acad. 1973, 73 (17), 291-297
  10. ↑ O'Callaghan, Conor N. (1980). "Isomerisation of 2-aryl-4-oxo-2,3-dihydrobenzopyrano[2,3-d]pyrimidines to 2-aryl-4-hydroxy-5H-benzopyrano[2,3-d]pyrimidines". Journal of the Chemical Society, Perkin Transactions 1. Royal Society of Chemistry (RSC): 1335-1337. doi:10.1039/p19800001335. ISSN 0300-922X.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.