133567-72-3Relevant academic research and scientific papers
1,5-Diphenylpenta-2,4-dien-1-ones as potent and selective monoamine oxidase-B inhibitors
Desideri, Nicoletta,Fioravanti, Rossella,Proietti Monaco, Luca,Biava, Mariangela,Yanez, Matilde,Ortuso, Francesco,Alcaro, Stefano
, p. 91 - 100 (2013/03/13)
A series of (2E,4E)-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-ones (3a-r) and (2Z,4E)-3-hydroxy-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-ones (6a-l) were synthesized and evaluated in vitro as inhibitors of the two human Monoamine oxidase (hMAO) iso
Novel (E)- and (Z)-2-styrylchromones from (E,E)-2′-hydroxycinnamylideneacetophenones - Xanthones from daylight photooxidative cyclization of (E)-2-styrylchromones
Silva, Artur M. S.,Pinto, Diana C. G. A.,Tavares, Hilario R.,Cavaleiro, Jose A. S.,Jimeno, M. Luisa,Elguero, Jose
, p. 2031 - 2038 (2007/10/03)
The oxidative cyclization of (E,E)-2′-hydroxycinnamylideneacetophenones 1a-e, and (E,E)-2′-benzyloxy-6′-hydroxycinnamylideneacetophenones 1i-1 with DMSO/ iodine, gave (E)-2-styrylchromones 3a-e,i-1. However, in the case of (E,E)-γ-alkyl-2′-hydroxycinnamyl
Synthesis of (E)-2-Styrylchromones
Cavaleiro, Jose A. S.,Elguero, Jose,Jimeno, M. Luisa,Silva, Artur M. S.
, p. 445 - 446 (2007/10/02)
A new synthesis of (E)-2-styrylchromones has been developed in paralell with synthetic studies on several flavone derivatives.
