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J. Tois, M. Vahermo and A. Koskinen, “Novel and Convenient Synthesis of 4(1H)quinolones,” Tetrahedron Letter, Vol. 46, No. 5, 2005, pp. 735-737.

has been cited by the following article:

• TITLE: New and Facile Synthesis of Substituted Pyrrole, Pyridine, Pyrazolo[4,3-b] Pyridine, Pyrano[3,2-c] Quinoline, Napthopyran, Naphthodipyran and Coumarin Derivatives

  AUTHORS: F. M. A. El-Taweel, A. A. Elagamey

  KEYWORDS: Pyrrole; Pyridine; Pyrazolo[4, 3-b] Pyridine; Pyrano[3, 2-c] Quinoline; Naphthopyran; Naphthodipyrans and Coumarin

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.3 No.1, March 27, 2013

  ABSTRACT: Several new pyrazolo[4,3-b] pyridines 7a, b were prepared by reacting arylidenemalononitriles 1a, c or 1i, j with 4-nitrosoantipyrine 4. Reacting 1a, b, d with 4-azidomethylcarbonylantipyrine 8 give 2-aminopyrrole 14. Pyrano[3,2-c] quinolines 20a, b and 23 were obtained by reacting 4-hydroxyquinoline 15 with 1g, h, 2b respectively. Reaction of 1 with naphthalenediols 24, 27 and 29 yield naphthodipyrans 26a, b, 28a, b and 30a,