Synthesis of Substituted Diazino[c]quinolin-5(6H)-ones, Diazino[c]isoquinolin-6(5H)-ones, Diazino[c]naphthyridin-6(5H)-ones and Diazino[c]naphthyridin-5(6H)-ones
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[1] Y. Charnay,et al. Synthesis and structure-affinity relationships of selective high-affinity 5-HT(4) receptor antagonists: application to the design of new potential single photon emission computed tomography tracers. , 2012, Journal of medicinal chemistry.
[2] Adam Siddiqui-Jain,et al. Novel potent dual inhibitors of CK2 and Pim kinases with antiproliferative activity against cancer cells. , 2012, Bioorganic & medicinal chemistry letters.
[3] T. Cailly,et al. N-tosylcarboxamide as a transformable directing group for Pd-catalyzed C-H ortho-arylation. , 2012, Organic letters.
[4] Chien‐Hong Cheng,et al. Synthesis of phenanthridinones from N-methoxybenzamides and arenes by multiple palladium-catalyzed C-H activation steps at room temperature. , 2011, Angewandte Chemie.
[5] Adam Siddiqui-Jain,et al. Novel potent pyrimido[4,5-c]quinoline inhibitors of protein kinase CK2: SAR and preliminary assessment of their analgesic and anti-viral properties. , 2011, Bioorganic & medicinal chemistry letters.
[6] Tingting Yuan,et al. One-pot formation of C-C and C-N bonds through palladium-catalyzed dual C-H activation: synthesis of phenanthridinones. , 2011, Angewandte Chemie.
[7] Adam Siddiqui-Jain,et al. Discovery and SAR of 5-(3-chlorophenylamino)benzo[c][2,6]naphthyridine-8-carboxylic acid (CX-4945), the first clinical stage inhibitor of protein kinase CK2 for the treatment of cancer. , 2011, Journal of medicinal chemistry.
[8] T. Roisnel,et al. Deprotonative metalation of substituted benzenes and heteroaromatics using amino/alkyl mixed lithium-zinc combinations. , 2010, Chemistry.
[9] S. Rault,et al. General method for the synthesis of substituted phenanthridin-6(5H)-ones using a KOH-mediated anionic ring closure as the key step , 2010 .
[10] M. Begtrup,et al. Regioselective functionalization of 2-(2′-fluorophenyl)-3-cyanopyridine and its cyclization to benzo[h]-1,6-naphthyridines , 2010 .
[11] F. Tillequin,et al. Synthesis of N-substituted benzo[c][1,7]- and benzo[c][1,8] phenanthrolin-(5H)-6-ones through a Pd-mediated Suzuki–Miyaura heteroaryl-aryl coupling reaction , 2009 .
[12] E. LaVoie,et al. 12-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridines as novel topoisomerase I-targeting antitumor agents. , 2009, Bioorganic & medicinal chemistry.
[13] A. Derdour,et al. Deprotonative cadmation of functionalized aromatics. , 2008, Chemical communications.
[14] C. Chai,et al. Structure-activity relationship studies of phenanthridine-based Bcl-XL inhibitors. , 2008, Journal of medicinal chemistry.
[15] E. LaVoie,et al. Synthesis of N-substituted 5-[2-(N-alkylamino)ethyl]dibenzo[c,h][1,6]naphthyridines as novel topoisomerase I-targeting antitumor agents. , 2008, Bioorganic & medicinal chemistry.
[16] E. LaVoie,et al. Facile formation of hydrophilic derivatives of 5H-8,9-dimethoxy-5-[2-(N,N-dimethylamino)ethyl]-2,3-methylenedioxydibenzo[c,h] [1,6]naphthyridin-6-one (ARC-111) and its 12-aza analog via quaternary ammonium intermediates. , 2008, Bioorganic & medicinal chemistry letters.
[17] R. Calhelha,et al. New strategies for the synthesis of heteroannulated 2-pyridinones, substituted 2-quinolinones and coumarins from dehydroamino acid derivatives , 2008 .
[18] W. Wilson,et al. Antitumor polycyclic acridines. 20. Search for DNA quadruplex binding selectivity in a series of 8,13-dimethylquino[4,3,2-kl]acridinium salts: telomere-targeted agents. , 2008, Journal of medicinal chemistry.
[19] M. Vaultier,et al. Lithium-mediated zincation of pyrazine, pyridazine, pyrimidine, and quinoxaline. , 2007, The Journal of organic chemistry.
[20] S. Rault,et al. The synthesis of three new heterocycles: the pyrido[4,3 or 3,4 or 2,3-c]-1,5-naphthyridines , 2007 .
[21] L. Bouffier,et al. Amino- and glycoconjugates of pyrido[4,3,2-kl]acridine. Synthesis, antitumor activity, and DNA binding. , 2006, Bioorganic & medicinal chemistry.
[22] S. Rault,et al. A new, direct, and efficient synthesis of benzonaphthyridin-5-ones , 2006 .
[23] E. Borowski,et al. 2,7-Dihydro-3H-pyridazino[5,4,3-kl]acridin-3-one derivatives, novel type of cytotoxic agents active on multidrug-resistant cell lines. Synthesis and biological evaluation. , 2005, Bioorganic & medicinal chemistry.
[24] M. Darabantu,et al. Synthesis of new polyaza heterocycles. Part 42: Diazines , 2005 .
[25] S. Buchwald,et al. Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure. , 2005, Journal of the American Chemical Society.
[26] A. Turck,et al. Regioselective synthesis and metallation of tributylstannylfluoropyrazines. Application to the synthesis of some new fluorinated liquid crystals diazines. Part 34 , 2003 .
[27] Mark T. Kershaw,et al. Synthesis of 2-aryl-oxazolo[4,5-c]quinoline-4(5H)-ones and 2-aryl-thiazolo[4,5-c]quinoline-4(5H)-ones. , 2003, Organic letters.
[28] Jie Zhang,et al. Design and synthesis of poly ADP-ribose polymerase-1 inhibitors. 2. Biological evaluation of aza-5[H]-phenanthridin-6-ones as potent, aqueous-soluble compounds for the treatment of ischemic injuries. , 2003, Journal of medicinal chemistry.
[29] P. Renard,et al. New benzo[h][1,6]naphthyridine and azepino[3,2-c]quinoline derivatives as selective antagonists of 5-HT4 receptors: binding profile and pharmacological characterization. , 2003, Journal of medicinal chemistry.
[30] Corinne Fruit,et al. Syntheses and metalation of pyridazinecarboxamides and thiocarboxamides. Diazines. Part 32 , 2002 .
[31] Norio Miyaura,et al. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds , 1995 .
[32] V. Snieckus,et al. Combined Metalation-Palladium-Catalyzed Cross Coupling Strategies. A Formal Synthesis of the Marine Alkaloid Amphimedine , 1995 .
[33] N. Haider,et al. On the metalation of 3-substituted and 3,6-disubstituted pyridazines , 1993 .
[34] W. Denny,et al. Potential antitumor agents. 55. 6-Phenylphenanthridine-4-carboxamides: a new class of DNA-intercalating antitumor agents. , 1988, Journal of medicinal chemistry.