Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1, 2, 4, 5, and 9.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya & Hou, Ai-Jun, 2020, Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides, pp. 1-11 in Phytochemistry (112524) 180 on page 4, DOI: 10.1016/j.phytochem.2020.112524, http://zenodo.org/record/829268
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 4, 6, and 7.Published as part of Liu, H...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou,...
Fig. 3. Key NOESY correlations of 1, 2, and 4.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yon...
Fig. 5. X-ray ORTEP drawing for 2a.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun,...
Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya, Hou, Ai-Jun (2020): Mer...
Fig. 6. ΔδH(S R) values (in ppm) for (S)-/(R)-MTPA esters of 8a and 8b′.Published as part of Shi, Qi...
Fig. 4. Chiral resolution chromatograms (A and C) and ECD spectra (B and D) for 1a/1b 8a/8b.Publishe...
Fig. 3. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zh...
Fig. 7. Compounds 5a, 8b, and 9 suppress the LPS-induced inflammatory responses in RAW 264.7 macroph...
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–11.Published as part of Huang, Wei-ming,...
Fig. 3. Key 2D correlations of 2.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou, Xing-cun, P...
Fig. 2. 1H–1H COSY and selective HMBC correlations for 1, 3/4, 10, and 13.Published as part of Youn,...
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 4, 6, and 7.Published as part of Liu, H...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou,...
Fig. 3. Key NOESY correlations of 1, 2, and 4.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yon...
Fig. 5. X-ray ORTEP drawing for 2a.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun,...
Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya, Hou, Ai-Jun (2020): Mer...
Fig. 6. ΔδH(S R) values (in ppm) for (S)-/(R)-MTPA esters of 8a and 8b′.Published as part of Shi, Qi...
Fig. 4. Chiral resolution chromatograms (A and C) and ECD spectra (B and D) for 1a/1b 8a/8b.Publishe...
Fig. 3. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zh...
Fig. 7. Compounds 5a, 8b, and 9 suppress the LPS-induced inflammatory responses in RAW 264.7 macroph...
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–11.Published as part of Huang, Wei-ming,...
Fig. 3. Key 2D correlations of 2.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou, Xing-cun, P...
Fig. 2. 1H–1H COSY and selective HMBC correlations for 1, 3/4, 10, and 13.Published as part of Youn,...
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 4, 6, and 7.Published as part of Liu, H...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou,...