Fig. 3. Key NOE correlations (red dotted double arrows and blue dotted double arrows) of aglycones of 2–4. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)Published as part of Chen, Ze-Ping, Guo, Lin-Bo, He, Jun, Xu, Jie-Kun, Li, Ya-Nan, Huang, Xiu-Yong, Li, Zi-Wei, Zhang, Wei-Ku & Tian, Hai-Yan, 2020, Triterpene saponins from the seeds of Erythrophleum fordii and their cytotoxic activities, pp. 1-7 in Phytochemistry (112428) 177 on page 5, DOI: 10.1016/j.phytochem.2020.112428, http://zenodo.org/record/829581
Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.Published as part of Xu, Zhen-Peng, Liu, Y...
Fig. 6. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
Fig. 2. COSY (bold lines) and key HMBC (H→C) correlations of 1 and 2.Published as part of Chen, Ze-P...
Fig. 1. Chemical structures of 1–7.Published as part of Chen, Ze-Ping, Guo, Lin-Bo, He, Jun, Xu, Jie...
Chen, Ze-Ping, Guo, Lin-Bo, He, Jun, Xu, Jie-Kun, Li, Ya-Nan, Huang, Xiu-Yong, Li, Zi-Wei, Zhang, We...
Fig. 3. Selected key NOE correlations (red dotted arrows) of aglycones of 2 (A) and of 12 (B). (For ...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Key NOESY correlations of compounds 4, 9, 11, 14 (R ¼ (CH2)14CH3, in green), 18 and 19. (For...
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key ROESY correlations of compounds 1–12.Published as part of Zang, Yi, Zhou, Beiping, Wei, ...
Fig. 7. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. Key HMBC (red arrows) and COSY (bold blue lines) correlations for compounds 1–7. (For interp...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.Published as part of Xu, Zhen-Peng, Liu, Y...
Fig. 6. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
Fig. 2. COSY (bold lines) and key HMBC (H→C) correlations of 1 and 2.Published as part of Chen, Ze-P...
Fig. 1. Chemical structures of 1–7.Published as part of Chen, Ze-Ping, Guo, Lin-Bo, He, Jun, Xu, Jie...
Chen, Ze-Ping, Guo, Lin-Bo, He, Jun, Xu, Jie-Kun, Li, Ya-Nan, Huang, Xiu-Yong, Li, Zi-Wei, Zhang, We...
Fig. 3. Selected key NOE correlations (red dotted arrows) of aglycones of 2 (A) and of 12 (B). (For ...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Key NOESY correlations of compounds 4, 9, 11, 14 (R ¼ (CH2)14CH3, in green), 18 and 19. (For...
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key ROESY correlations of compounds 1–12.Published as part of Zang, Yi, Zhou, Beiping, Wei, ...
Fig. 7. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. Key HMBC (red arrows) and COSY (bold blue lines) correlations for compounds 1–7. (For interp...
Fig. 3. Key NOESY correlations of compounds 1, 2, 4 and 7.Published as part of Xu, Zhen-Peng, Liu, Y...
Fig. 6. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...