Fig. 4. Selected 2D NMR correlations of compound 8.Published as part of Gao, Yuan, Zhou, Jun-Su, Liu, Hong-Chun, Zhang, Yan, Yin, Wei-Hang, Liu, Qun-Fang, Wang, Guan-Wu, Zhao, Jin-Xin & Yue, Jian-Min, 2022, Phorneroids A-M, diverse types of diterpenoids from Euphorbia neriifolia, pp. 1-11 in Phytochemistry (113142) 198 on page 5, DOI: 10.1016/j.phytochem.2022.113142, http://zenodo.org/record/823527
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...
Fig. 3. Selected 2D NMR correlations of compound 5.Published as part of Gao, Yuan, Zhou, Jun-Su, Liu...
Fig. 5. Selected 2D NMR correlations of compound 12.Published as part of Gao, Yuan, Zhou, Jun-Su, Li...
Fig. 2. Selected 2D NMR correlations of compound 1.Published as part of Gao, Yuan, Zhou, Jun-Su, Liu...
Fig. 7. Experimental and calculated ECD spectra of compounds 2 (A), 3 (B), 8 (C), and 12 (D).Publish...
Gao, Yuan, Zhou, Jun-Su, Liu, Hong-Chun, Zhang, Yan, Yin, Wei-Hang, Liu, Qun-Fang, Wang, Guan-Wu, Zh...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 2. 1 H– 1 H COSY and key HMBC correlations of compounds 1–3.Published as part of Li, Jian-Chun,...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7.Published as part of Chang, Ste...
Fig. 5. 1H NMR spectra and assignments of compounds 1–3.Published as part of Chang, Stephen S., Huan...
Fig. 3. Key NOE correlations of compounds 1, 3, 6, and 7.Published as part of Chang, Stephen S., Hua...
Fig. 1. Structures of compounds 1–12 isolated from Euphorbia neriifolia.Published as part of Li, Jia...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...
Fig. 3. Selected 2D NMR correlations of compound 5.Published as part of Gao, Yuan, Zhou, Jun-Su, Liu...
Fig. 5. Selected 2D NMR correlations of compound 12.Published as part of Gao, Yuan, Zhou, Jun-Su, Li...
Fig. 2. Selected 2D NMR correlations of compound 1.Published as part of Gao, Yuan, Zhou, Jun-Su, Liu...
Fig. 7. Experimental and calculated ECD spectra of compounds 2 (A), 3 (B), 8 (C), and 12 (D).Publish...
Gao, Yuan, Zhou, Jun-Su, Liu, Hong-Chun, Zhang, Yan, Yin, Wei-Hang, Liu, Qun-Fang, Wang, Guan-Wu, Zh...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 2. 1 H– 1 H COSY and key HMBC correlations of compounds 1–3.Published as part of Li, Jian-Chun,...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7.Published as part of Chang, Ste...
Fig. 5. 1H NMR spectra and assignments of compounds 1–3.Published as part of Chang, Stephen S., Huan...
Fig. 3. Key NOE correlations of compounds 1, 3, 6, and 7.Published as part of Chang, Stephen S., Hua...
Fig. 1. Structures of compounds 1–12 isolated from Euphorbia neriifolia.Published as part of Li, Jia...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...