Fig. 3. (A) Chiral-phase HPLC chromatograms of (±)-1 and (±)-2. (B) Experimental and calculated ECD spectra of (+)-1/()-1 and (+)-2/()-2.Published as part of Huang, Guo-Yong, Cui, Hui, Lu, Xin-Yi, Zhang, Lu-Di, Ding, Xiao-Ying, Wu, Jin-Jun, Duan, Li-Xin, Zhang, Shi-Jie, Liu, Zhongqiu & Zhang, Rong-Rong, 2021, (þ/¡)-Dievodialetins A¡G: Seven pairs of enantiomeric coumarin dimers with anti-acetylcholinesterase activity from the roots of Evodia lepta Merr., pp. 1-7 in Phytochemistry (112597) 182 on page 3, DOI: 10.1016/j.phytochem.2020.112597, http://zenodo.org/record/829146
Fig. 8. Experimental ECD spectra of zephyranines G–I (7–9), 6-O-ethylnerinine (10) and the calculate...
Two polyprenylated acylcyclopentanone racemates, evodialones A (<b>1</b>) and B (<b>2</b>), featurin...
Fig. 4. (A) The CD exciton chirality model for 1 and 2; (B)–(F) The calculated ECD spectra of 1 (B),...
Huang, Guo-Yong, Cui, Hui, Lu, Xin-Yi, Zhang, Lu-Di, Ding, Xiao-Ying, Wu, Jin-Jun, Duan, Li-Xin, Zha...
Fig. 1. Chemical structures of 1 9.Published as part of Huang, Guo-Yong, Cui, Hui, Lu, Xin-Yi, Zhang...
Fig. 2. (A) Key 1H–1H COSY (red bold lines) and HMBC (blue arrows) correlations of 1. (B) X-ray ORTE...
Fig. 4. Plausible biosynthetic pathway of (+/)-1 7.Published as part of Huang, Guo-Yong, Cui, Hui, L...
Fig. 5. Compounds 1–9 ameliorate oxidative stress and neuroinflammation in scopolamine-treated SH-SY...
Fig. 3. Calculated and experimental ECD spectra (a) and chiral analysis chromatogram (b) of 1a and 1...
Fig. 4. Comparisons of calculated ECD spectra and experimental ECD spectra of compounds 3–5. (A) The...
Fig. 4. Chiral resolution chromatograms (A and C) and ECD spectra (B and D) for 1a/1b 8a/8b.Publishe...
Fig. 2. Comparison of experimental and calculated ECD spectra of compounds 3–12. * Mirror image (ena...
Fig. 4. Experimental and calculated ECD spectra of zephyranines A (1) and B (2) and their enantiomer...
Fig. 3. X-ray structures of (+)-1 (A) and ()-1 (B), and experimental and calculated ECD spectra of (...
Fig. 7. Experimental and calculated ECD spectra of zephyranines C F (3–6), isolated as mixtures of r...
Fig. 8. Experimental ECD spectra of zephyranines G–I (7–9), 6-O-ethylnerinine (10) and the calculate...
Two polyprenylated acylcyclopentanone racemates, evodialones A (<b>1</b>) and B (<b>2</b>), featurin...
Fig. 4. (A) The CD exciton chirality model for 1 and 2; (B)–(F) The calculated ECD spectra of 1 (B),...
Huang, Guo-Yong, Cui, Hui, Lu, Xin-Yi, Zhang, Lu-Di, Ding, Xiao-Ying, Wu, Jin-Jun, Duan, Li-Xin, Zha...
Fig. 1. Chemical structures of 1 9.Published as part of Huang, Guo-Yong, Cui, Hui, Lu, Xin-Yi, Zhang...
Fig. 2. (A) Key 1H–1H COSY (red bold lines) and HMBC (blue arrows) correlations of 1. (B) X-ray ORTE...
Fig. 4. Plausible biosynthetic pathway of (+/)-1 7.Published as part of Huang, Guo-Yong, Cui, Hui, L...
Fig. 5. Compounds 1–9 ameliorate oxidative stress and neuroinflammation in scopolamine-treated SH-SY...
Fig. 3. Calculated and experimental ECD spectra (a) and chiral analysis chromatogram (b) of 1a and 1...
Fig. 4. Comparisons of calculated ECD spectra and experimental ECD spectra of compounds 3–5. (A) The...
Fig. 4. Chiral resolution chromatograms (A and C) and ECD spectra (B and D) for 1a/1b 8a/8b.Publishe...
Fig. 2. Comparison of experimental and calculated ECD spectra of compounds 3–12. * Mirror image (ena...
Fig. 4. Experimental and calculated ECD spectra of zephyranines A (1) and B (2) and their enantiomer...
Fig. 3. X-ray structures of (+)-1 (A) and ()-1 (B), and experimental and calculated ECD spectra of (...
Fig. 7. Experimental and calculated ECD spectra of zephyranines C F (3–6), isolated as mixtures of r...
Fig. 8. Experimental ECD spectra of zephyranines G–I (7–9), 6-O-ethylnerinine (10) and the calculate...
Two polyprenylated acylcyclopentanone racemates, evodialones A (<b>1</b>) and B (<b>2</b>), featurin...
Fig. 4. (A) The CD exciton chirality model for 1 and 2; (B)–(F) The calculated ECD spectra of 1 (B),...