1373820-97-3Relevant academic research and scientific papers
Synthesis of 3-aryl-2-methoxyinden-1-one (Z)-phenylhydrazones via hydrobromic acid-mediated cyclization of 2-(1-aryl-2-methoxyethenyl)benzaldehyde phenylhydrazones
Kobayashi, Kazuhiro,Miyatani, Wataru,Matsumoto, Naoki
, p. 239 - 245 (2013/03/28)
2-(1-Aryl-2-methoxyethenyl)benzaldehydes 2, obtained by successive treatment of 1-(1-aryl-2-methoxyethenyl)-2-bromobenzenes 1 with BuLi and 1-formylpiperidine, were transformed to the corresponding phenylhydrazones 3 on treatment with PhNHNH2.
Synthesis of 4-arylisocoumarins (=4-aryl-1H-2-benzopyran-1-ones) through acidic hydrolysis of (Z)-2-(1-aryl-2-methoxyethenyl)benzaldehydes, followed by oxidation
Kobayashi, Kazuhiro,Miyatani, Wataru,Kuroda, Minami
, p. 2173 - 2178 (2014/01/06)
4-Arylisocoumarins (=4-aryl-1H-2-benzopyran-1-ones) 6 were prepared from 2-(1-aryl-2-methoxyethenyl)-1-bromobenzenes 1. Successive treatment of these bromo styrenes with BuLi and 1-formylpiperidine gave a mixture of (E)- and (Z)-2-(1-aryl-2-methoxyethenyl)benzaldehydes 2. Hydrolysis of (Z)-isomers with conc. HBr, followed by pyridinium chlorochromate (PCC) oxidation of the resulting 1H-2-benzopyran-1-ol derivatives 4 (and 5), afforded the desired products. Copyright
Synthesis of polysubstituted isoquinolines through cross-coupling reactions with α-alkoxytosylhydrazones
Florentino, Lucia,Aznar, Fernando,Valdes, Carlos
, p. 2323 - 2325 (2012/06/18)
A Pd-catalyzed cross-coupling reaction of α-alkoxytosylhydrazones with sulfonates derived from salicyl aldehydes gives rise to protected 1,5-dicarbonyl compounds. Treatment with ammonium hydroxide readily transforms these alkenes into isoquinolines with d
