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kw.\*:("1,7-Naphtyridine dérivé")

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Syntheses of naphthonaphthyridines by Skraup reaction using 3-aminobenzo[g or h]quinolineTAKEUCHI, I; HAMADA, Y; HIROTA, M et al.Chemical and pharmaceutical bulletin. 1993, Vol 41, Num 4, pp 747-751, issn 0009-2363Article

Synthesis and NMR spectra of the six isomeric thieno[c]-fused 1,7- and 1,8-naphthyridinesMALM, J; REHN, B; HÖRNFELDT, A.-B et al.Journal of heterocyclic chemistry. 1994, Vol 31, Num 1, pp 11-15, issn 0022-152XArticle

De l'ortho-lithiation de dérivés iodés aza-aromatiques en général, et de l'application à la synthèse de 2,9-diazaphénanthrènes en particulier = Iodo-directed ortho-lithiation of aza-aromatics and application to the synthesis of 2,9-diazaphenanthrenesCochennec, Corine; Queguiner, G.1994, 247 p.Thesis

Synthesis of four isomeric imidazonaphthyridines: three novel ring systemsGRIVAS, S; RONNE, E.Journal of chemical research. Synopses (Print). 1994, Num 7, pp 268-269, issn 0308-2342Article

Cyclobutene Ring-Opening of Bicyclo[4.2.0]octa-1,6-dienes: Access to CF3-Substituted 5,6,7,8-Tetrahydro-1,7-naphthyridinesMAILYAN, Artur K; PEREGUDOV, Alexander S; DIXNEUF, Pierre H et al.Journal of organic chemistry. 2012, Vol 77, Num 19, pp 8518-8526, issn 0022-3263, 9 p.Article

Discovery and SAR of novel, potent and selective hexahydrobenzonaphthyridinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)TORRISI, Caterina; BISBOCCI, Monica; INGENITO, Raffaele et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 2, pp 448-452, issn 0960-894X, 5 p.Article

Design and structure-activity relationship of heterocyclic analogs of 4-amino-3-benzimidazol-2-ylhydroquinolin-2-ones as inhibitors of receptor tyrosine kinasesFRAZIER, Kelly; JAZAN, Elisa; LAPOINTE, Gena et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 8, pp 2247-2251, issn 0960-894X, 5 p.Article

Palladium-catalyzed cross-coupling reactions for the synthesis of 6,8-disubstituted 1,7-naphthyridines : A novel class of potent and selective phosphodiesterase type 4D inhibitorsHERSPERGER, R; BRAY-FRENCH, K; MAZZONI, L et al.Journal of medicinal chemistry (Print). 2000, Vol 43, Num 4, pp 675-682, issn 0022-2623Article

Synthesis of 4-(8-benzo[1,2,5]oxadiazol-5-yl-[1,7]naphthyridine-6-yl)-benzoic acid: a potent and selective phosphodiesterase type 4D inhibitorHERSPERGER, Rene; DAWSON, Janet; MUELLER, Thomas et al.Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 2, pp 233-235, issn 0960-894XArticle

Acetic Anhydride Generated Imidazolium Ylide in Ring Closures onto Carboxylic Acids; Part of the Synthesis of New Potential Bioreductive Antitumor AgentsJOYCE, Eamonn; MCARDLE, Patrick; ALDABBAGH, Fawaz et al.Synlett (Stuttgart). 2011, Num 8, pp 1097-1100, issn 0936-5214, 4 p.Article

Novel imidazo[1,2-a]naphthyridinic systems (part 1) : Synthesis, antiproliferative and DNA-intercalating activitiesANDALOUSSI, Mounir; MOREAU, Emmanuel; CHAVIGNON, Olivier et al.European journal of medicinal chemistry. 2008, Vol 43, Num 11, pp 2505-2517, issn 0223-5234, 13 p.Article

Synthesis and Nicotinic Acetylcholine Receptor Binding Properties of Bridged and Fused Ring Analogues of EpibatidineCARROLL, F. Ivy; ROBINSON, T. Philip; BRIEADDY, Lawrence E et al.Journal of medicinal chemistry (Print). 2007, Vol 50, Num 25, pp 6383-6391, issn 0022-2623, 9 p.Article

Synthesis and antitumor activity of some new substituted quinolin-4-one and 1,7-naphthyridin-4-one analogsEL-SUBBAGH, H. I; ABADI, A. H; AL-KHAWAD, I. E et al.Archiv der Pharmazie (Weinheim). 1999, Vol 332, Num 1, pp 19-24, issn 0365-6233Article

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