87884-43-3Relevant academic research and scientific papers
Mizoroki-Heck cross-couplings of 2-acetyl-5-bromobenzofuran and aryl halides under microwave irradiation
Shaaban, Mohamed R.,Darweesh, Ahmed F.,Dawood, Kamal M.,Faraga, Ahmad M.
experimental part, p. 208 - 225 (2011/02/22)
Mizoroki-Heck cross-coupling reactions of 2-acetyl-5-bromobenzofuran as well as activated and deactivated aryl bromides with various olefins were investigated under both thermal as well as microwave irradiating conditions in open air using water solvent.
Antiulcer Agents. 4. Conformational Considerations and the Antiulcer Activity of Substituted Imidazopyridines and Related Analogues
Kaminski, James J.,Puchalski, Chester,Solomon, Daniel M.,Rizvi, Razia K.,Conn, David J.,et al.
, p. 1686 - 1700 (2007/10/02)
Definition of the interrelationship between the conformational characteristics of a series of substituted imidazopyridines and their antiulcer activity was investigated by examining the conformational properties of 3-cyano-2-methyl-8-(phenylmethoxy
Antiallergic agents. III. N-(1H-tetrazol-5-yl)-2-pyridinecarboxamides
Honma,Hanamoto,Hashiyama,et al.
, p. 125 - 128 (2007/10/02)
A series of N-tetrazolylpyridinecarboxamides was prepared and evaluated for antiallergic activity by the passive cutaneous anaphylaxis assay. From the structure-activity relationships of this class of compounds, it was revealed that the N-tetrazolylcarbamoyl group as an acidic functionality is required to be at the 2-position of the pyridine nucleus and that the phenyl group as a substituent is not necessarily required for activity. 6-Methyl-N-(1H-tetrazol-5-yl)-2-pyridinecarboxamide showed good oral activity and low toxicity.
