Fig. 7. Key 1H–1H COSY, HMBC and NOEs/ROESY correlations of compounds 6–9.Published as part of Zhang, Jian-Pei, Li, Wen-Rui, Wu, Shuo, Wang, Xiao-Jing, Wang, Ru-Bing, Li, Mi, Su, Guo-Zhu, Wang, Hai-Qiang, Yong, Jin-Yao, Yang, Jia, Li, Li, Li, Yu-Huan & Ma, Shuang-Gang, 2021, Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity, pp. 1-11 in Phytochemistry (112935) 192 on page 7, DOI: 10.1016/j.phytochem.2021.112935, http://zenodo.org/record/825748
Fig. 3. The ORTEP drawing of illisimonone A (1).Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao...
Fig. 3. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 2 and 3.Published ...
Fig. 2. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compound 1.Published as part...
Fig. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 8. Key 1H–1H COSY, HMBC and ROESY correlations of compounds 10 and 10a.Published as part of Zha...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 2. Key HMBC correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, Wen-Rui, Wu...
Fig. 1. Structures of prenylated C6–C3 compounds 1–13.Published as part of Zhang, Jian-Pei, Li, Wen-...
Fig. 4. CD spectra of compounds 1–5, 7, 8, 10a, 11, 12, and 13 in MeOH.Published as part of Zhang, J...
Zhang, Jian-Pei, Li, Wen-Rui, Wu, Shuo, Wang, Xiao-Jing, Wang, Ru-Bing, Li, Mi, Su, Guo-Zhu, Wang, H...
Fig. 5. Single-crystal X-ray structure of compound 1.Published as part of Zhang, Jian-Pei, Li, Wen-R...
Fig. 6. The experimental ECD spectra of 2, 6, and 8 (red) and the calculated ECD spectra of 2, 6, an...
Fig. 10. Proposed biogenetic pathway for compounds 1–13.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 1. The structures of compounds 1–11.Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao-Jing, ...
Fig. 5. The experimental ECD spectra of 3 and 4 and calculated ECD spectra of a pair of enantiomers ...
Fig. 3. The ORTEP drawing of illisimonone A (1).Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao...
Fig. 3. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 2 and 3.Published ...
Fig. 2. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compound 1.Published as part...
Fig. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 8. Key 1H–1H COSY, HMBC and ROESY correlations of compounds 10 and 10a.Published as part of Zha...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 2. Key HMBC correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, Wen-Rui, Wu...
Fig. 1. Structures of prenylated C6–C3 compounds 1–13.Published as part of Zhang, Jian-Pei, Li, Wen-...
Fig. 4. CD spectra of compounds 1–5, 7, 8, 10a, 11, 12, and 13 in MeOH.Published as part of Zhang, J...
Zhang, Jian-Pei, Li, Wen-Rui, Wu, Shuo, Wang, Xiao-Jing, Wang, Ru-Bing, Li, Mi, Su, Guo-Zhu, Wang, H...
Fig. 5. Single-crystal X-ray structure of compound 1.Published as part of Zhang, Jian-Pei, Li, Wen-R...
Fig. 6. The experimental ECD spectra of 2, 6, and 8 (red) and the calculated ECD spectra of 2, 6, an...
Fig. 10. Proposed biogenetic pathway for compounds 1–13.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 1. The structures of compounds 1–11.Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao-Jing, ...
Fig. 5. The experimental ECD spectra of 3 and 4 and calculated ECD spectra of a pair of enantiomers ...
Fig. 3. The ORTEP drawing of illisimonone A (1).Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao...
Fig. 3. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 2 and 3.Published ...
Fig. 2. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compound 1.Published as part...