164408-48-4Relevant academic research and scientific papers
Synthesis of two alnustone-like natural diarylheptanoids via 4+3 strategy
Burmaoglu, Serdar,Celik, Huelya,Goeiksu, Sueleyman,Maras, Ahmet,Altundas, Ramazan,Secen, Hasan
experimental part, p. 1549 - 1562 (2009/11/30)
The first total synthesis of (4E,6E)-1,7-bis(3,4-dihydroxyphenyl)-hepta-4, 6-dien-3-one and an alternative synthesis of (4E,6E)-1,7-bis(4-hydroxyphenyl)- hepta-4,6-dien-3-one, two natural diarylheptanoids, mainly based on Claisen-Schmidt condensation were described. The crucial steps of the syntheses were the condensation of OH-protected 4-aryl-2-butanones with OH-protected 3-aryl-acrylaldehydes by the in situ enamination and then deprotection of OH groups to give the corresponding natural diarylheptanoids. Copyright Taylor & Francis Group, LLC.
A Series of (4-Arylbutadienyl)oxazolochromones with Highly Potent 5-Lipoxygenase Inhibitory Activity
Kosaka,Takatoshi,Ochiai, Keiko,Wakabayashi, Toshio,Murota, Sei-itsu
, p. 502 - 514 (2007/10/03)
A series of (4-arylbutadienyl)oxazolochromone was synthesized and evaluated for their inhibitory activity of 5-lipoxygenase. These compounds were found to be potent 5-lipoxygenase inhibitors and many were better than TMK-777, one of the most potent compou
