Fig. 3. Key NOESY correlations of compounds 1–4, 5 and 6 (1D NOESY correlations were marked in red and 2D NOESY correlations were marked in blue).Published as part of Yan, Zhi-Yang, Lv, Tian-Ming, Wang, Yu-Xi, Shi, Shao-Chun, Chen, Jing-Jie, Bin-Lin, Liu, Qing-Bo, Huang, Xiao-Xiao & Song, Shao-Jiang, 2020, Terpenylated coumarins from the root bark of Ailanthus altissima (Mill.) Swingle, pp. 1-9 in Phytochemistry (112361) 175 on page 4, DOI: 10.1016/j.phytochem.2020.112361, http://zenodo.org/record/829543
Fig. 3. Key NOE correlations (red dotted double arrows and blue dotted double arrows) of aglycones o...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Zhou, Ming, Peng, Xiaogang, Zho...
Fig. 2. Key HMBC correlations (arrows in blue) and H1–H1 COSY (bold bond in black) of the undescribe...
Fig. 4. (A) Possible gross structures of compounds 3, 4 and 11; (B) Possible relative configurations...
Fig. 1. Chemical structure of compounds 1–14.Published as part of Yan, Zhi-Yang, Lv, Tian-Ming, Wang...
Yan, Zhi-Yang, Lv, Tian-Ming, Wang, Yu-Xi, Shi, Shao-Chun, Chen, Jing-Jie, Bin-Lin, Liu, Qing-Bo, Hu...
Fig. 5. ΔδS-R value (ppm) of MTPA ester of 3, 5, 6 and 10.Published as part of Yan, Zhi-Yang, Lv, Ti...
Four new terpenylated coumarins (<b>1</b>–<b>4</b>) were isolated from the stem bark of <i>Ailanthus...
Fig. 2. Key NOESY correlations for 1.Published as part of Singh, Ahilya, Cullen, Jason K., Bruce, Za...
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
The present study was focussed to carry out the detailed pharmacognostic studies in terms of organol...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
Fig. 3. Selected NOESY correlations (H↔H) of 1, 2, 10 and 14.Published as part of Wang, Xue, Jin, Xu...
Fig. 3. Key NOESY correlations of 1, 2, 5 and 6.Published as part of Ablajan, Nurfida, Zhao, Bo, Zha...
Fig. 3. Key NOE correlations (red dotted double arrows and blue dotted double arrows) of aglycones o...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Zhou, Ming, Peng, Xiaogang, Zho...
Fig. 2. Key HMBC correlations (arrows in blue) and H1–H1 COSY (bold bond in black) of the undescribe...
Fig. 4. (A) Possible gross structures of compounds 3, 4 and 11; (B) Possible relative configurations...
Fig. 1. Chemical structure of compounds 1–14.Published as part of Yan, Zhi-Yang, Lv, Tian-Ming, Wang...
Yan, Zhi-Yang, Lv, Tian-Ming, Wang, Yu-Xi, Shi, Shao-Chun, Chen, Jing-Jie, Bin-Lin, Liu, Qing-Bo, Hu...
Fig. 5. ΔδS-R value (ppm) of MTPA ester of 3, 5, 6 and 10.Published as part of Yan, Zhi-Yang, Lv, Ti...
Four new terpenylated coumarins (<b>1</b>–<b>4</b>) were isolated from the stem bark of <i>Ailanthus...
Fig. 2. Key NOESY correlations for 1.Published as part of Singh, Ahilya, Cullen, Jason K., Bruce, Za...
Fig. 3. The key NOESY correlations of compounds 1–4.Published as part of Li, Qin, Zheng, Yuyi, Fu, A...
The present study was focussed to carry out the detailed pharmacognostic studies in terms of organol...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
Fig. 3. Selected NOESY correlations (H↔H) of 1, 2, 10 and 14.Published as part of Wang, Xue, Jin, Xu...
Fig. 3. Key NOESY correlations of 1, 2, 5 and 6.Published as part of Ablajan, Nurfida, Zhao, Bo, Zha...
Fig. 3. Key NOE correlations (red dotted double arrows and blue dotted double arrows) of aglycones o...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Zhou, Ming, Peng, Xiaogang, Zho...