41514-36-7Relevant academic research and scientific papers
Determination of free diferulic, disinapic and dicoumaric acids in plants and foods
Grúz, Ji?í,Pospí?il, Ji?í,Kozubíková, Hana,Pospí?il, Tomá?,Dole?al, Karel,Bunzel, Mirko,Strnad, Miroslav
, p. 280 - 286 (2015/03/18)
Hydroxycinnamates are common phenolic compounds of plants and plant foods, often found in substantial quantities. Due to their high in vitro antioxidant activity they can easily be oxidized under oxidative conditions. In this study, we found that in vitro
Hydroxycinnamic acids as DNA-cleaving agents in the presence of Cu II ions: Mechanism, structure-activity relationship, and biological implications
Fan, Gui-Juan,Jin, Xiao-Ling,Qian, Yi-Ping,Wang, Qi,Yang, Ru-Ting,Dai, Fang,Tang, Jiang-Jiang,Shang, Ya-Jing,Cheng, Li-Xia,Yang, Jie,Zhou, Bo
experimental part, p. 12889 - 12899 (2010/06/16)
The effectiveness of hydroxycinnamic acids (HCAs), that is, caffeic acid (CaA), chlorogenic acid (ChA), sinapic acid (SA), ferulic acid (FA), 3hydroxycinnamic acid (3-HCA), and 4hydroxycinnamic acid (4-HCA), as pBR322 plasmid DNA-cleaving agents in the pr
Stereochemistry of phellinsin A: A concise synthesis of α-arylidene-γ-lactones
Kim, Eungsoo,Hyeong, Kyu Lee,Hwang, Eui-Il,Kim, Sung-Uk,Woo, Song Lee,Lee, Sangku,Jung, Sang-Hun
, p. 1231 - 1238 (2007/10/03)
Phellinsin A (1a) was prepared in a concise way, thereby elucidating the relative stereochemistry of the aryl and carboxylic acid groups in 1a. The synthesis employed selective monohydrolysis of the dilactones derived from oxidative dimerization of cinnamic acid derivatives. This approach provided a practical synthetic route to α-arylidene-γ-lactones. Copyright Taylor & Francis, Inc.
