Synthesis and Cytotoxicity of (±)-9-Hydroxy-5-oxo-2,3,4,5-tetrahydro-1H -benzo[b ]azepine-2-carboxamide: An Active Component of Juglans regia

[1]  Xiao-guang Chen,et al.  Azacyclo-indoles and Phenolics from the Flowers of Juglans regia. , 2017, Journal of natural products.

[2]  K. Mukkanti,et al.  Apparent Carbon Monoxide InsertionviaDouble Isocyanide Incorporation during Palladium-Catalyzed Construction of Indoloquinoline Ring in a Single Pot: Synthesis of New Cytotoxic Agents , 2016 .

[3]  Rajnikanth Sunke,et al.  Copper‐Catalyzed Domino Reaction Involving Nitro as an Unexpected Leaving Group: Construction of Dibenzo‐Fused Azepinone Ring , 2016 .

[4]  N. Panth,et al.  Phytochemical profile and biological activity of Juglans regia. , 2016, Journal of integrative medicine.

[5]  S. Ito,et al.  Stereochemistry of N-Benzoyl-5-substituted-1-benzazepines Revisited: Synthesis of the Conformationally Biased Derivatives and Revision of the Reported Structure. , 2016, The Journal of organic chemistry.

[6]  M. Pal,et al.  Creation of molecular complexities via a new Cu-catalyzed cascade reaction: a direct access to novel 2,2'-spirobiindole derivatives. , 2015, Chemical communications.

[7]  Q. Dang,et al.  A cascade of acid-promoted C-O bond cleavage and redox reactions: from oxa-bridged benzazepines to benzazepinones. , 2014, Organic letters.

[8]  B. Matuszczak,et al.  Synthesis of substituted 3-(3-chloro-1H-pyrazol-5-yl)quinoxalin-2(1H)ones , 2014 .

[9]  Sun Choi,et al.  The carbonate analogues of 5'-halogenated resiniferatoxin as TRPV1 ligands. , 2013, European journal of medicinal chemistry.

[10]  Israel Fernández,et al.  Intramolecular Pd(0)-catalyzed reactions of (2-iodoanilino)-aldehydes: a joint experimental-computational study. , 2012, The Journal of organic chemistry.

[11]  Waya S. Phutdhawong,et al.  Synthesis and anticancer activity of 5,6,8,13-tetrahydro-7H-naphtho[2,3-a][3]-benzazepine-8,13-diones , 2012, Archives of pharmacal research.

[12]  D. Adams,et al.  Phosphodiesterase inhibitors. Part 3: Design, synthesis and structure-activity relationships of dual PDE3/4-inhibitory fused bicyclic heteroaromatic-dihydropyridazinones with anti-inflammatory and bronchodilatory activity. , 2012, Bioorganic & medicinal chemistry.

[13]  D. Spring,et al.  Novel and efficient copper-catalysed synthesis of nitrogen-linked medium-ring biaryls. , 2011, Chemistry.

[14]  K. Niknam,et al.  Silica-bonded S-sulfonic acid: an efficient and recyclable solid acid catalyst for the three-component synthesis of α-amino nitriles , 2010 .

[15]  B. T. Bagmanov Effect of structural factors and solvent nature in bromination of anilines , 2009 .

[16]  J. Ghali,et al.  Conivaptan: A Dual Receptor Vasopressin V1a/V2 Antagonist , 2007 .

[17]  H. Fujiki,et al.  Tolvaptan, an orally active vasopressin V(2)-receptor antagonist - pharmacology and clinical trials. , 2007, Cardiovascular drug reviews.

[18]  M. Paris,et al.  Polymer-supported organotin reagents for regioselective halogenation of aromatic amines. , 2005, The Journal of organic chemistry.

[19]  Y. Yamamura,et al.  7-Chloro-5-hydroxy-1-[2-methyl-4-(2-methylbenzoyl-amino)benzoyl ]-2,3,4,5-tetrahydro-1H-1-benzazepine (OPC-41061): a potent, orally active nonpeptide arginine vasopressin V2 receptor antagonist. , 1999, Bioorganic & medicinal chemistry.

[20]  Y. Yamamura,et al.  Orally active, nonpeptide vasopressin V2 receptor antagonists: a novel series of 1-[4-(benzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepines and related compounds. , 1996, Journal of medicinal chemistry.

[21]  M. Fujikawa,et al.  Halogenation Using Quaternary Ammonium Polyhalides. VI. Bromination of Aromatic Amines by Use of Benzyltrimethylammonium Tribromide , 1988 .

[22]  T. Mosmann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. , 1983, Journal of immunological methods.

[23]  V. Boekelheide,et al.  The Synthesis of 1-Benzazepine Derivatives as Model Compounds Related to Apo-β-Erythroidine1,2 , 1955 .