898547-02-9Relevant academic research and scientific papers
Systematic Asymmetric Synthesis of All Diastereomers of (-)-Talaumidin and Their Neurotrophic Activity
Harada, Kenichi,Kubo, Miwa,Horiuchi, Hiroki,Ishii, Akiko,Esumi, Tomoyuki,Hioki, Hideaki,Fukuyama, Yoshiyasu
, p. 7076 - 7088 (2015/07/28)
(-)-Talaumidin (1), a 2,5-biaryl-3,4-dimethyltetrahydrofuran lignan isolated from Aristolochia arcuata Masters, shows significant neurite-outgrowth promotion and neuroprotection in primary cultured rat cortical neurons and in NGF-differentiated PC12 cells
Asymmetric synthesis of (+)-machilin f by unusual stereoselective mitsunobu reaction
Harada, Kenichi,Kubo, Naoko,Tanabe, Kazuma,Kubo, Miwa,Esumi, Tomoyuki,Hioki, Hideaki,Fukuyama, Yoshiyasu
, p. 1127 - 1132 (2011/05/05)
First synthesis of (+)-machilin F (1c) has been achieved in 16 steps as part of systematic synthetic studies on (-)-talaumidin (1) and its stereoisomers. The 2,3,4,5-tetrasubstituted tetrahydrofuran with the (2S,3S,4S,5S)-configuration has been constructe
First enantioselective synthesis of (-)-talaumidin, a neurotrophic diaryltetrahydrofuran-type lignan
Esumi, Tomoyuki,Hojyo, Daisuke,Zhai, Haifeng,Fukuyama, Yoshiyasu
, p. 3979 - 3983 (2007/10/03)
The first enantioselective total synthesis of a neurotrophic (-)-talaumidin (1) is described in 16 steps from 4-benzyloxy-3-methoxybenzaldehyde in ca. 10.7% overall yield, and thus has established the absolute configurations of the four stereogenic center
