Systematic Asymmetric Synthesis of All Diastereomers of (-)-Talaumidin and Their Neurotrophic Activity.

(-)-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. The four stereogenic centers on the tetrahydrofuran moiety in 1 result in the presence of seven diastereomers except for their enantiomers. In order to investigate the stereochemistry-activity relationships of the stereoisomers, the systematic synthesis of all stereoisomers of 1 was accomplished by employing Evans aldol, diastereoselective hydroboration, reductive deoxygenation, and Mitsunobu reactions as key steps.

Nanofluids alter the surface wettability of solids.

We report the results of our studies on the changes in the contact angle and interfacial tension using a nanofluid composed of silica nanoparticles dispersed in water on three different solid substrates: gold (partially hydrophobic), glass (hydrophilic), and a silicon wafer (hydrophilic). We used both the goniometric method and drop-shape analysis to make the measurements. On the basis of the results of the drop-shape analysis using the Laplace equation, we evaluated the contributions of the interfacial tension change to the equilibrium contact angle and the presence of nanoparticles near the solid substrate, thereby elucidating the change in the wettability of the solid substrate.