Fig. 3. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 2 and 3.Published as part of Liu, Yang-Lan, Li, Wen-Rui, Wang, Xiao-Jing, Wang, Ru-Bing, Li, Mi, Zhang, Jian-Pei, Yong, Jing-Yao, Bao, Xiu-Qi, Zhang, Dan & Ma, Shuang-Gang, 2020, Highly oxidized sesquiterpenes from the fruits of Illicium lanceolatum A. C. Smith, pp. 1-11 in Phytochemistry (112281) 172 on page 4, DOI: 10.1016/j.phytochem.2020.112281, http://zenodo.org/record/829415
Fig. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 7. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 9 and 10.Published...
Fig. 2. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compound 1.Published as part...
Fig. 5. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 4 and 5.Published ...
Fig. 6. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 6, 7 and 8.Publish...
Fig. 1. Structures of compounds 1–16.Published as part of Liu, Yang-Lan, Li, Wen-Rui, Wang, Xiao-Jin...
Liu, Yang-Lan, Li, Wen-Rui, Wang, Xiao-Jing, Wang, Ru-Bing, Li, Mi, Zhang, Jian-Pei, Yong, Jing-Yao,...
Fig. 4. Single-crystal X-ray crystallographic structures of compounds 3 (left) and 6 (right).Publish...
Fig. 8. Single-crystal X-ray crystallographic structure of compound 9.Published as part of Liu, Yang...
Fig. 9. Plausible biosynthetic pathways for seco-prezizaane-type sesquiterpenes 1–3, and 6–16 and al...
Fig. 10. Protection rate of resveratrol (RSV) and compounds 2–4, 6–9 and 11–16 against monosodium gl...
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. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...
Fig. 7. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 9 and 10.Published...
Fig. 2. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compound 1.Published as part...
Fig. 5. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 4 and 5.Published ...
Fig. 6. 1H–1H COSY, key HMBC and selected NOE and ROESY correlations of compounds 6, 7 and 8.Publish...
Fig. 1. Structures of compounds 1–16.Published as part of Liu, Yang-Lan, Li, Wen-Rui, Wang, Xiao-Jin...
Liu, Yang-Lan, Li, Wen-Rui, Wang, Xiao-Jing, Wang, Ru-Bing, Li, Mi, Zhang, Jian-Pei, Yong, Jing-Yao,...
Fig. 4. Single-crystal X-ray crystallographic structures of compounds 3 (left) and 6 (right).Publish...
Fig. 8. Single-crystal X-ray crystallographic structure of compound 9.Published as part of Liu, Yang...
Fig. 9. Plausible biosynthetic pathways for seco-prezizaane-type sesquiterpenes 1–3, and 6–16 and al...
Fig. 10. Protection rate of resveratrol (RSV) and compounds 2–4, 6–9 and 11–16 against monosodium gl...
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. 9. Key 1H–1H COSY and HMBC correlations of compounds 11 12.Published as part of Zhang, Jian-Pei...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 3. Key ROESY and NOE correlations of compounds 1–5.Published as part of Zhang, Jian-Pei, Li, We...