Fig. 3. Selected 2D NMR correlations of compound 5.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. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 6. CD spectrum of 4 in DMSO containing Mo2(OAc)4 with the inherent CDs subtracted.Published as ...
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. 4. Selected 2D NMR correlations of compound 8.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. 5. 1H NMR spectra and assignments of compounds 1–3.Published as part of Chang, Stephen S., Huan...
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. 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. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 6. CD spectrum of 4 in DMSO containing Mo2(OAc)4 with the inherent CDs subtracted.Published as ...
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. 4. Selected 2D NMR correlations of compound 8.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. 5. 1H NMR spectra and assignments of compounds 1–3.Published as part of Chang, Stephen S., Huan...
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. 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. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 6. CD spectrum of 4 in DMSO containing Mo2(OAc)4 with the inherent CDs subtracted.Published as ...