Fig. 3. Key 1H–1H COSY (red bold lines) and HMBC (blue→) of compound 9 (a), NOSEY correlation (blue→) of compound 9 (b), The ORTEP drawing of compound 9 (c). (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 4, DOI: 10.1016/j.phytochem.2022.113113, http://zenodo.org/record/823523
Fig. 5. Experimental CD spectrum (red line) of compound 2, and the Rh2(OCOCF3)4 induced CD spectrum ...
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 NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Fig. 4. Key 1H–1H COSY (red bold lines) and HMBC (blue→) correlation of compounds 11 (a), 12 (b), 13...
Chen, Yan-Yan, Zeng, Xiao-Tao, Xu, Ding-Qiao, Yue, Shi-Jun, Fu, Rui-Jia, Yang, Xue, Liu, Zhao-Xi, Ta...
Fig. 2. Key 1H–1H COSY (blue bold bonds) and HMBC (red arrows) correlations of 1–7. (For interpretat...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 3. ORTEP drawing for compound 1.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 5. ORTEP drawing for compound 6.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...
Fig. 6. Pimarane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 6. Experimental ECD spectrum of 3 (red line) and calculated ECD spectra (200–400 nm) of (3S,4S,...
Fig. 5. Experimental CD spectrum (red line) of compound 2, and the Rh2(OCOCF3)4 induced CD spectrum ...
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 NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key 1 H– 1 H COSY (red bold lines) and HMBC (blue→) of compounds 5 (a1) and 16 (a2), NOSEY c...
Fig. 4. Key 1H–1H COSY (red bold lines) and HMBC (blue→) correlation of compounds 11 (a), 12 (b), 13...
Chen, Yan-Yan, Zeng, Xiao-Tao, Xu, Ding-Qiao, Yue, Shi-Jun, Fu, Rui-Jia, Yang, Xue, Liu, Zhao-Xi, Ta...
Fig. 2. Key 1H–1H COSY (blue bold bonds) and HMBC (red arrows) correlations of 1–7. (For interpretat...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 3. ORTEP drawing for compound 1.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 5. ORTEP drawing for compound 6.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.Published as part of Du, Kaicheng, Yang, Xinyo...
Fig. 6. Pimarane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 3. Key ROESY correlations of compounds 1, 2, 4 and 5.Published as part of Li, Jian-Chun, Dai, W...
Fig. 6. Experimental ECD spectrum of 3 (red line) and calculated ECD spectra (200–400 nm) of (3S,4S,...
Fig. 5. Experimental CD spectrum (red line) of compound 2, and the Rh2(OCOCF3)4 induced CD spectrum ...
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 NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...