Fig. 4. Key 1H–1H COSY (red bold lines) and HMBC (blue→) correlation of compounds 11 (a), 12 (b), 13 (c), and 15 (d). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)Published as part of Chen, Yan-Yan, Zeng, Xiao-Tao, Xu, Ding-Qiao, Yue, Shi-Jun, Fu, Rui-Jia, Yang, Xue, Liu, Zhao-Xi & Tang, Yu-Ping, 2022, Pimarane, abietane, and labdane diterpenoids from Euphorbia pekinensis Rupr. and their anti-tumor activities, pp. 1-8 in Phytochemistry (113113) 197 on page 5, DOI: 10.1016/j.phytochem.2022.113113, http://zenodo.org/record/823523
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key correlations in HMBC (red arrows) and 1H–1H COSY (black bold) of 1–4, 16, 20, and 21. (F...
Fig. 6. Experimental ECD spectrum of 3 (red line) and calculated ECD spectra (200–400 nm) of (3S,4S,...
Fig. 3. Key 1H–1H COSY (red bold lines) and HMBC (blue→) of compound 9 (a), NOSEY correlation (blue→...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Chen, Yan-Yan, Zeng, Xiao-Tao, Xu, Ding-Qiao, Yue, Shi-Jun, Fu, Rui-Jia, Yang, Xue, Liu, Zhao-Xi, Ta...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 2. Key 1H–1H COSY (blue bold bonds) and HMBC (red arrows) correlations of 1–7. (For interpretat...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...
Fig. 2. 1 H– 1 H COSY and key HMBC correlations of compounds 1–3.Published as part of Li, Jian-Chun,...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 6. Pimarane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...
Fig. 2. Key COSY (H→H) and HMBC (H→C) correlations of compounds 1–7.Published as part of Meng, Xian-...
Fig. 3. Key NOESY (H→H) correlations of compounds 1–7.Published as part of Meng, Xian-Hua, Wang, Kai...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key correlations in HMBC (red arrows) and 1H–1H COSY (black bold) of 1–4, 16, 20, and 21. (F...
Fig. 6. Experimental ECD spectrum of 3 (red line) and calculated ECD spectra (200–400 nm) of (3S,4S,...
Fig. 3. Key 1H–1H COSY (red bold lines) and HMBC (blue→) of compound 9 (a), NOSEY correlation (blue→...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Chen, Yan-Yan, Zeng, Xiao-Tao, Xu, Ding-Qiao, Yue, Shi-Jun, Fu, Rui-Jia, Yang, Xue, Liu, Zhao-Xi, Ta...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 2. Key 1H–1H COSY (blue bold bonds) and HMBC (red arrows) correlations of 1–7. (For interpretat...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...
Fig. 2. 1 H– 1 H COSY and key HMBC correlations of compounds 1–3.Published as part of Li, Jian-Chun,...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 6. Pimarane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...
Fig. 2. Key COSY (H→H) and HMBC (H→C) correlations of compounds 1–7.Published as part of Meng, Xian-...
Fig. 3. Key NOESY (H→H) correlations of compounds 1–7.Published as part of Meng, Xian-Hua, Wang, Kai...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key correlations in HMBC (red arrows) and 1H–1H COSY (black bold) of 1–4, 16, 20, and 21. (F...
Fig. 6. Experimental ECD spectrum of 3 (red line) and calculated ECD spectra (200–400 nm) of (3S,4S,...