Fig. 8. The HMBC and key NOE correlations of 7.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wang, Xue, Suo, Xinyue, Lin, Mingbao, Jiang, Jiandong & Ji, Tengfei, 2021, Polycyclic polyprenylated acylphloroglucinol derivatives from Hypericum pseudohenryi, pp. 1-8 in Phytochemistry (112761) 187 on page 6, DOI: 10.1016/j.phytochem.2021.112761, http://zenodo.org/record/825900
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 7. Linear correlation between experimental and calculated 13C NMR chemical shifts of 5 at the B...
Fig. 9. The anti-inflammatory activity of compound 1–13.Published as part of Sun, Haoran, Wang, Jiaj...
Fig. 7. Key HMBC and NOE correlations of 6.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo,...
Fig. 6. 1H–1H COSY, Key HMBC and NOE correlations of 5.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 4. 1H–1H COSY, Key HMBC and NOE correlations of 3.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 2. 1H–1H COSY, Key HMBC and NOE correlations of 1.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 3. Key NOE correlations of 2 and 4.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wa...
Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wang, Xue, Suo, Xinyue, Lin, Mingbao, Jiang, Jiandong, Ji, Teng...
Fig. 5. Selected NOESY correlations of 3 and 4.Published as part of Fang, Qiang-Qiang, Feng, Tong-To...
Fig. 1. Structures of compound 1–7.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wang, X...
Fig. 8. Key 2D correlations of compounds 7 and 8.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 5. Calculated ECD spectra of 1 and 3.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, ...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 7. Linear correlation between experimental and calculated 13C NMR chemical shifts of 5 at the B...
Fig. 9. The anti-inflammatory activity of compound 1–13.Published as part of Sun, Haoran, Wang, Jiaj...
Fig. 7. Key HMBC and NOE correlations of 6.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo,...
Fig. 6. 1H–1H COSY, Key HMBC and NOE correlations of 5.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 4. 1H–1H COSY, Key HMBC and NOE correlations of 3.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 2. 1H–1H COSY, Key HMBC and NOE correlations of 1.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 3. Key NOE correlations of 2 and 4.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wa...
Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wang, Xue, Suo, Xinyue, Lin, Mingbao, Jiang, Jiandong, Ji, Teng...
Fig. 5. Selected NOESY correlations of 3 and 4.Published as part of Fang, Qiang-Qiang, Feng, Tong-To...
Fig. 1. Structures of compound 1–7.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wang, X...
Fig. 8. Key 2D correlations of compounds 7 and 8.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 5. Calculated ECD spectra of 1 and 3.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, ...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 7. Linear correlation between experimental and calculated 13C NMR chemical shifts of 5 at the B...
Fig. 9. The anti-inflammatory activity of compound 1–13.Published as part of Sun, Haoran, Wang, Jiaj...