Fig. 3. Key NOESY correlations of 1, 2, and 4.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. 3. Key NOESY correlations for 1, 3/4, 10, and 13.Published as part of Youn, Isoo, Han, Kyu-Yeon...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou,...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1, 2, 4, 5, and 9.Published as part of Shi, Qing,...
Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya, Hou, Ai-Jun (2020): Mer...
Fig. 5. X-ray ORTEP drawing for 2a.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun,...
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. 7. Compounds 5a, 8b, and 9 suppress the LPS-induced inflammatory responses in RAW 264.7 macroph...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
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 key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yu...
Fig. 3. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zh...
Fig. 1. Structures of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan, Wen-Cong, ...
Fig. 3. Key NOESY correlations for 1, 3/4, 10, and 13.Published as part of Youn, Isoo, Han, Kyu-Yeon...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou,...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1, 2, 4, 5, and 9.Published as part of Shi, Qing,...
Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya, Hou, Ai-Jun (2020): Mer...
Fig. 5. X-ray ORTEP drawing for 2a.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun,...
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. 7. Compounds 5a, 8b, and 9 suppress the LPS-induced inflammatory responses in RAW 264.7 macroph...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
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 key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yu...
Fig. 3. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zh...
Fig. 1. Structures of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan, Wen-Cong, ...
Fig. 3. Key NOESY correlations for 1, 3/4, 10, and 13.Published as part of Youn, Isoo, Han, Kyu-Yeon...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Deng, Xin, Xia, Jing, Hu, Bo, Hou,...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...