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. Phytochemistry (112935) 192: 1-11, DOI: 10.1016/j.phytochem.2021.112935, URL: http://dx.doi.org/10.1016/j.phytochem.2021.11293
Fig. 3. The ORTEP drawing of illisimonone A (1).Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao...
Fig. 5. The experimental ECD spectra of 3 and 4 and calculated ECD spectra of a pair of enantiomers ...
Fig. 4. The experimental and calculated ECD spectra of 2a and 2b.Published as part of Su, Guo-Zhu, L...
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...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 2. Key HMBC correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, Wen-Rui, Wu...
Fig. 7. Key 1H–1H COSY, HMBC and NOEs/ROESY correlations of compounds 6–9.Published as part of Zhang...
Fig. 8. Key 1H–1H COSY, HMBC and ROESY correlations of compounds 10 and 10a.Published as part of Zha...
Fig. 5. Single-crystal X-ray structure of compound 1.Published as part of Zhang, Jian-Pei, Li, Wen-R...
Fig. 10. Proposed biogenetic pathway for compounds 1–13.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 6. The experimental ECD spectra of 2, 6, and 8 (red) and the calculated ECD spectra of 2, 6, an...
Fig. 1. The structures of compounds 1–11.Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao-Jing, ...
Su, Guo-Zhu, Li, Mi, Wang, Xiao-Jing, Wang, Ru-Bing, Ma, Shuang-Gang, Zhang, Dan, Wang, Xiao-Liang, ...
Fig. 3. The ORTEP drawing of illisimonone A (1).Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao...
Fig. 5. The experimental ECD spectra of 3 and 4 and calculated ECD spectra of a pair of enantiomers ...
Fig. 4. The experimental and calculated ECD spectra of 2a and 2b.Published as part of Su, Guo-Zhu, L...
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...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 2. Key HMBC correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, Wen-Rui, Wu...
Fig. 7. Key 1H–1H COSY, HMBC and NOEs/ROESY correlations of compounds 6–9.Published as part of Zhang...
Fig. 8. Key 1H–1H COSY, HMBC and ROESY correlations of compounds 10 and 10a.Published as part of Zha...
Fig. 5. Single-crystal X-ray structure of compound 1.Published as part of Zhang, Jian-Pei, Li, Wen-R...
Fig. 10. Proposed biogenetic pathway for compounds 1–13.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 6. The experimental ECD spectra of 2, 6, and 8 (red) and the calculated ECD spectra of 2, 6, an...
Fig. 1. The structures of compounds 1–11.Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao-Jing, ...
Su, Guo-Zhu, Li, Mi, Wang, Xiao-Jing, Wang, Ru-Bing, Ma, Shuang-Gang, Zhang, Dan, Wang, Xiao-Liang, ...
Fig. 3. The ORTEP drawing of illisimonone A (1).Published as part of Su, Guo-Zhu, Li, Mi, Wang, Xiao...
Fig. 5. The experimental ECD spectra of 3 and 4 and calculated ECD spectra of a pair of enantiomers ...
Fig. 4. The experimental and calculated ECD spectra of 2a and 2b.Published as part of Su, Guo-Zhu, L...