Fig. 3. ORTEP drawing for compound 1.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Feng, Lei, Wang, Chao & Ma, Xiao-Chi, 2021, Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities, pp. 1-8 in Phytochemistry (112593) 183 on page 3, DOI: 10.1016/j.phytochem.2020.112593, http://zenodo.org/record/829195
Fig. 8. ORTEP diagram of 6.Published as part of Yu, Hang-Fei, Cheng, Yu-Chen, Wu, Cai-Meng, Ran, Kun...
Fig. 7. ORTEP diagram of 5.Published as part of Yu, Hang-Fei, Cheng, Yu-Chen, Wu, Cai-Meng, Ran, Kun...
Fig. 4. Abietane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...
Fig. 5. ORTEP drawing for compound 6.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 1. Structure of compounds 1–15.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, ...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 4. The ORTEP drawing of 1.Published as part of Wei, Jiang-Chun, Zhang, Xiao-Yu, Gao, Yu-Ning, W...
Fig. 4. Measured ECD and calculated ECD spectra of compounds 2–5 together with their stereoisomers.P...
Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Fen...
Fig. 6. The inhibitory effects of diterpenoids 1–15 on HCE 2 (a). The inhibitory effects of diterpen...
Fig. 5. Proposed biosynthetic pathway for 1.Published as part of Wei, Jiang-Chun, Zhang, Xiao-Yu, Ga...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 1. Two ways of diterpenoid cyclization.Published as part of Xu, Yang, Tang, Peiyu, Zhu, Man, Wa...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key 1H–1H COSY, and HMBC correlations of compounds 1–8.Published as part of Wei, Jiang-Chun,...
Fig. 8. ORTEP diagram of 6.Published as part of Yu, Hang-Fei, Cheng, Yu-Chen, Wu, Cai-Meng, Ran, Kun...
Fig. 7. ORTEP diagram of 5.Published as part of Yu, Hang-Fei, Cheng, Yu-Chen, Wu, Cai-Meng, Ran, Kun...
Fig. 4. Abietane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...
Fig. 5. ORTEP drawing for compound 6.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han,...
Fig. 1. Structure of compounds 1–15.Published as part of Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, ...
Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.Published as part...
Fig. 4. The ORTEP drawing of 1.Published as part of Wei, Jiang-Chun, Zhang, Xiao-Yu, Gao, Yu-Ning, W...
Fig. 4. Measured ECD and calculated ECD spectra of compounds 2–5 together with their stereoisomers.P...
Li, Da-Wei, Deng, Xiao-Peng, He, Xin, Han, Xiu-Yan, Ma, Yu-Fang, Huang, Hui-Lian, Yu, Zhen-Long, Fen...
Fig. 6. The inhibitory effects of diterpenoids 1–15 on HCE 2 (a). The inhibitory effects of diterpen...
Fig. 5. Proposed biosynthetic pathway for 1.Published as part of Wei, Jiang-Chun, Zhang, Xiao-Yu, Ga...
Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.Published as part of Li, Jian-Chun, Dai, ...
Fig. 1. Two ways of diterpenoid cyclization.Published as part of Xu, Yang, Tang, Peiyu, Zhu, Man, Wa...
Fig. 3. Key NOE correlations of Compounds 1 and 5.Published as part of Du, Kaicheng, Yang, Xinyong, ...
Fig. 2. Key 1H–1H COSY, and HMBC correlations of compounds 1–8.Published as part of Wei, Jiang-Chun,...
Fig. 8. ORTEP diagram of 6.Published as part of Yu, Hang-Fei, Cheng, Yu-Chen, Wu, Cai-Meng, Ran, Kun...
Fig. 7. ORTEP diagram of 5.Published as part of Yu, Hang-Fei, Cheng, Yu-Chen, Wu, Cai-Meng, Ran, Kun...
Fig. 4. Abietane diterpenoids isolated from E. ebracteolata.Published as part of Yang, Ting, He, Jun...