80825-32-7Relevant academic research and scientific papers
Synthesis and anti-inflammatory activity of phenylbutenoid dimer analogs
Kim, Sung-Soo,Fang, Yuanying,Park, Haeil
supporting information, p. 1676 - 1680 (2015/07/15)
Several phenylbutenoid dimer (PBD) analogs were synthesized and evaluated for their inhibitory activities against nitric oxide (NO) production and TNF-α release. The PBD analogs were synthesized via Diels - Alder and subsequent Schlosser reactions as key steps. Among the tested compounds, two analogs (8c, 8f) exhibited much stronger inhibitory activity against LPS-stimulated NO production and TNF-α release in RAW 264.7 cells than that of wogonin.
CHEMISTRY OF ENOL ETHERS. LIII. PROTOTROPIC ISOMERIZATION IN THE SERIES OF CYCLIC 1-ALKOXY-1,4-DIENES
Makin, S. M.,Pomogaev, A. I.,Boiko, T. N.,Nikiforova, A. P.
, p. 2033 - 2036 (2007/10/02)
A series of diethyl acetals of 1-cyclohexene-3-carbaldehydes, the pyrolysis of which leads to the formation of cyclic 1-ethoxy-1,4-dienes, were obtained by the acetalization of 1-cyclohexene-3-carbaldehydes, which were obtained by the condensation of conjugated dienes with α,β-unsaturated aldehydes.The prototropic isomerization of the 1-ethoxy-1,4-dienes to corresponding 1-ethoxy-1,3-dienes under the influence of potassium tert-butoxide in dimethyl sulfoxide solution was investigated.
