Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfei, Shi, Zhengyi, Cao, Yunfang, Zhang, Yeting, Hu, Hong, Tong, Qingyi, Qi, Changxing & Zhang, Yonghui, 2022, Kiiacylphnols A H, eight undescribed polycyclic polyprenylated acylphloroglucinols with anticancer activities from Hypericum przewalskii Maxim, pp. 1-11 in Phytochemistry (113166) 199 on page 6, DOI: 10.1016/j.phytochem.2022.113166, http://zenodo.org/record/823573
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 5. Selected NOESY correlations of 3 and 4.Published as part of Fang, Qiang-Qiang, Feng, Tong-To...
Fig. 8. The HMBC and key NOE correlations of 7.Published as part of Sun, Haoran, Wang, Jiajia, Zhen,...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 8. Key 2D correlations of compounds 7 and 8.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 1. Structures of compounds 1–10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfe...
Fig. 3. NMR calculations with DP4+ probability analysis of compounds 1 and 2.Published as part of Du...
Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfei, Shi, Zhengyi, Cao, Yunfang, Zhang, Yeting, Hu, Hong, To...
Fig. 9. Calculated ECD spectra of compound 7 and experimental ECD spectra of compounds 7 and 8.Publi...
Fig. 4. Experimental and calculated ECD spectra for compounds 1 and 4.Published as part of Duan, Yul...
Fig. 7. Single-crystal X-ray structure of 10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu...
Fig. 5. Experimental ECD spectra for compounds 1–6 and 9.Published as part of Duan, Yulin, Hu, Ping,...
Fig. 7. Key HMBC and NOE correlations of 6.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo,...
Fig. 3. Key NOE correlations of 2 and 4.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wa...
Fig. 6. 1H–1H COSY, Key HMBC and NOE correlations of 5.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 5. Selected NOESY correlations of 3 and 4.Published as part of Fang, Qiang-Qiang, Feng, Tong-To...
Fig. 8. The HMBC and key NOE correlations of 7.Published as part of Sun, Haoran, Wang, Jiajia, Zhen,...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 8. Key 2D correlations of compounds 7 and 8.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 1. Structures of compounds 1–10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfe...
Fig. 3. NMR calculations with DP4+ probability analysis of compounds 1 and 2.Published as part of Du...
Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfei, Shi, Zhengyi, Cao, Yunfang, Zhang, Yeting, Hu, Hong, To...
Fig. 9. Calculated ECD spectra of compound 7 and experimental ECD spectra of compounds 7 and 8.Publi...
Fig. 4. Experimental and calculated ECD spectra for compounds 1 and 4.Published as part of Duan, Yul...
Fig. 7. Single-crystal X-ray structure of 10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu...
Fig. 5. Experimental ECD spectra for compounds 1–6 and 9.Published as part of Duan, Yulin, Hu, Ping,...
Fig. 7. Key HMBC and NOE correlations of 6.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo,...
Fig. 3. Key NOE correlations of 2 and 4.Published as part of Sun, Haoran, Wang, Jiajia, Zhen, Bo, Wa...
Fig. 6. 1H–1H COSY, Key HMBC and NOE correlations of 5.Published as part of Sun, Haoran, Wang, Jiaji...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 5. Selected NOESY correlations of 3 and 4.Published as part of Fang, Qiang-Qiang, Feng, Tong-To...
Fig. 8. The HMBC and key NOE correlations of 7.Published as part of Sun, Haoran, Wang, Jiajia, Zhen,...