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Beilstein J. Org. Chem. 2026, 22, 691–704, doi:10.3762/bjoc.22.54
Graphical Abstract
Figure 1: Chemical structures of the two known natural products, (+)-salicifoliol (1) and (+)-pinoresinol (2)...
Figure 2: Reaction schemes detailing the semisynthesis of (+)-eudesmin (3), (+)-phillygenin (4), (+)-5,5'-dib...
Figure 3: Key COSY, HMBC, and ROESY correlations for (+)-5,5'-dibromopinoresinol (5).
Figure 4: ORTEP drawing of (+)-eudesmin (3).
Figure 5: ECD data for compounds 2–7 in MeOH.
Figure 6: Percentage of cell viability for (+)-pinoresinol (2) and its analogues (+)-eudesmin (3), (+)-philly...
Figure 7: (A) Transwell invasive assay of the (+)-pinoresinol library 2–7 on U251MG cells at a concentration ...
Figure 8: (A) Transwell invasion assay of (+)-4,4'-di(3,3-dimethylbutanoyl)pinoresinol (6) on KNS42 cells at ...
Figure 9: The U251 cell line was derived from a grade III–IV malignant tumor, specifically an astrocytoma, ob...