Fig. 3. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yuan, Rong-Wen, Deng, Li, Hou, Cheng, Li, Wei, Liu, Ting, Kong, Xiang-Qian, Zhang, Li-Jun & Liao, Hai-Bing, 2022, Terpenoids with α-glucosidase inhibitory activity from Rhododendron minutiflorum Hu, pp. 1-11 in Phytochemistry (113083) 196 on page 5, DOI: 10.1016/j.phytochem.2021.113083, http://zenodo.org/record/823448
Fig. 2. Selected key HMBC () and 1H–1H COSY () correlations of compounds 1, 5, 7, 9a/9b, and 10a/10b...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5.Published as part of Vo, Thanh-Hoa, Lin, ...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yu...
Fig. 6. Structure and α-glucosidase inhibitory activity relationship analysis.Published as part of F...
Fig. 5. X-ray ORTEP drawing of 1–2 and 6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yuan, Ron...
Fig. 1. Chemical structures of compounds 1–32.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yuan...
Fig. 2. Experimental ECD spectra of rhodominutinoid B–C (2–3) in MeOH.Published as part of Fan, Xian...
Fan, Xian-Zhe, Zhu, Yang-Li, Yuan, Rong-Wen, Deng, Li, Hou, Cheng, Li, Wei, Liu, Ting, Kong, Xiang-Q...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1, 2, 4, 5, and 9.Published as part of Shi, Qing,...
Fig. 2. Key 1H–1H COSY (blue bold bonds) and HMBC (red arrows) correlations of 1–7. (For interpretat...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 2. The key 1H-1H COSY and HMBC correlations of compounds 1–11.Published as part of He, Xiao-Fen...
Fig. 2. (A) 1H–1H COSY and key HMBC correlations for 1; (B) Selected ROESY correlations for 1.Publis...
Fig. 2. Selected key HMBC () and 1H–1H COSY () correlations of compounds 1, 5, 7, 9a/9b, and 10a/10b...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5.Published as part of Vo, Thanh-Hoa, Lin, ...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yu...
Fig. 6. Structure and α-glucosidase inhibitory activity relationship analysis.Published as part of F...
Fig. 5. X-ray ORTEP drawing of 1–2 and 6.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yuan, Ron...
Fig. 1. Chemical structures of compounds 1–32.Published as part of Fan, Xian-Zhe, Zhu, Yang-Li, Yuan...
Fig. 2. Experimental ECD spectra of rhodominutinoid B–C (2–3) in MeOH.Published as part of Fan, Xian...
Fan, Xian-Zhe, Zhu, Yang-Li, Yuan, Rong-Wen, Deng, Li, Hou, Cheng, Li, Wei, Liu, Ting, Kong, Xiang-Q...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1, 2, 4, 5, and 9.Published as part of Shi, Qing,...
Fig. 2. Key 1H–1H COSY (blue bold bonds) and HMBC (red arrows) correlations of 1–7. (For interpretat...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
Fig. 3. Key NOE correlations (blue dashed arrows) in 1–7. (For interpretation of the references to c...
Fig. 2. The key 1H-1H COSY and HMBC correlations of compounds 1–11.Published as part of He, Xiao-Fen...
Fig. 2. (A) 1H–1H COSY and key HMBC correlations for 1; (B) Selected ROESY correlations for 1.Publis...
Fig. 2. Selected key HMBC () and 1H–1H COSY () correlations of compounds 1, 5, 7, 9a/9b, and 10a/10b...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5.Published as part of Vo, Thanh-Hoa, Lin, ...