Synthesis of pyrano[3,2-c]quinoline-4-carboxylates and 2-(4-oxo-1,4-dihydroquinolin-3-yl)fumarates

[11] Radwan MF(2002)Synthesis of highly branched sulfur–nitrogen heterocycles by cascade cycloadditions of [1,2]dithiolo[1,4]thiazines and [1,2]dithiolopyrroles Bioorg Med Chem 10 2705-4251

[12] Gamal-Eldeen AM(2006)4-Hydroxy-3-nitro-2-quinolones and related compounds as inhibitors of allergic reactions Bioorg Med Chem Lett 16 4246-1181

[13] Abdel-Aziz M(1984)Design, synthesis, structural studies, biological evaluation, and computational simulations of novel potent AT J Heterocycl Chem 21 1177-5936

[14] Abuo-Rahma GA(2004) angiotensin II receptor antagonists based on the 4-phenylquinoline structure J Med 47 5923-1289

[15] Ramadan M(2012)Synthesis and cytotoxic activity evaluation of indolo-, pyrrolo-, and benzofuro-quinolin-2(1 J Heterocycl Chem 49 1269-5922

[16] Aly AA(2004))-ones and 6-anilinoindoloquinoline derivatives J Med Chem 47 5912-7782

[17] Brown AB(2006)Design, synthesis, and biological evaluations of novel quinolones as HIV-1 non-nucleoside reverse transcriptase inhibitors Tetrahedron Lett 47 7779-471

[18] Hassan AA(1996)Non-steroidal antiinflammatory agents. 1. Synthesis of 4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl alkanoic acids by the wittig reaction of quinisatines J Nat Prod 59 469-1886

[19] Asghari S(1997)Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 2 Bioorg Med Chem Lett 7 1883-606

[20] Ramezani S(1998)Synthesis and chemical reactivity of pyrano[3,2- Nat Prod Rep 15 595-704

[11] Radwan MF(2002)Synthesis of highly branched sulfur–nitrogen heterocycles by cascade cycloadditions of [1,2]dithiolo[1,4]thiazines and [1,2]dithiolopyrroles Bioorg Med Chem 10 2705-4251

[12] Gamal-Eldeen AM(2006)4-Hydroxy-3-nitro-2-quinolones and related compounds as inhibitors of allergic reactions Bioorg Med Chem Lett 16 4246-1181

[13] Abdel-Aziz M(1984)Design, synthesis, structural studies, biological evaluation, and computational simulations of novel potent AT J Heterocycl Chem 21 1177-5936

[14] Abuo-Rahma GA(2004) angiotensin II receptor antagonists based on the 4-phenylquinoline structure J Med 47 5923-1289

[15] Ramadan M(2012)Synthesis and cytotoxic activity evaluation of indolo-, pyrrolo-, and benzofuro-quinolin-2(1 J Heterocycl Chem 49 1269-5922

[16] Aly AA(2004))-ones and 6-anilinoindoloquinoline derivatives J Med Chem 47 5912-7782

[17] Brown AB(2006)Design, synthesis, and biological evaluations of novel quinolones as HIV-1 non-nucleoside reverse transcriptase inhibitors Tetrahedron Lett 47 7779-471

[18] Hassan AA(1996)Non-steroidal antiinflammatory agents. 1. Synthesis of 4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl alkanoic acids by the wittig reaction of quinisatines J Nat Prod 59 469-1886

[19] Asghari S(1997)Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 2 Bioorg Med Chem Lett 7 1883-606

[20] Ramezani S(1998)Synthesis and chemical reactivity of pyrano[3,2- Nat Prod Rep 15 595-704