60463-24-3Relevant academic research and scientific papers
The flavan-isoflavan rearrangement: Bioinspired synthetic access to isoflavonoids via 1,2-shift-alkylation sequence
Nakamura, Kayo,Ohmori, Ken,Suzuki, Keisuke
supporting information, p. 7012 - 7014 (2015/04/22)
An approach to 2-substituted isoflavonoids is reported based on the 1,2-shift of the aryl group in the catechin skeleton followed by the in situ alkylation. Synthesis of (-)-equol, a natural isoflavan with estrogenic activities, was achieved.
Synthesis and biological activity of cinnamaldehydes as angiogenesis inhibitors
Kwon, Byoung-Mog,Lee, Seung-Ho,Cho, Young-Kwon,Bok, Song-Hae,So, Seung-Ho,Youn, Mi-Ran,Chang, Soo-Ik
, p. 2473 - 2476 (2007/10/03)
A series of 2-hydroxycinnamaldehyde derivatives was synthesized for examing a structure-activity relationship for inhibition of angiogenesis. The anti-angiogenic effects of 2'-substituted cinnamaldehydes and related analogs were determined in a chick embryo chorioallantoic membrane assay system.
