Fig. 3. Key HMBC correlations of compounds 1–4.Published as part of Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xie, Jun, Lai, Shengtian, Wang, Hongqing, Chen, Ruoyun & Kang, Jie, 2021, The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L, pp. 1-9 in Phytochemistry (112622) 183 on page 5, DOI: 10.1016/j.phytochem.2020.112622, http://zenodo.org/record/829180
Fig. 2. Key HMBC correlations of compounds 1–10.Published as part of Xie, Jun, Wang, Hongqing, Dong,...
Fig. 2. Key HMBC correlations for compound 1.Published as part of Bendamene, Samia, Boutaghane, Naim...
Fig. 3. Key 1 H– 1 H COSY (blue arrows) and HMBC (red arrows) correlations in compounds 1 and 4. (Fo...
Fig. 1. Structures of compounds 1–4.Published as part of Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xie...
Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xie, Jun, Lai, Shengtian, Wang, Hongqing, Chen, Ruoyun, Kang...
Fig. 6. X-ray crystal structure of 4.Published as part of Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xi...
Fig. 4. Experimental ECD spectra obtained in MeOH and calculated ECD spectra for isomers 1–4 (a–d, r...
Fig. 2. Chiral HPLC-UV chromatogram of racemic 1–4 (a–d) using a Chiralpak AD-H column (4.6 mm × 250...
Fig. 2. Key HMBC correlations of compound 1a/1b‒12.Published as part of Yin, Zhao-Kun, Liu, Zhao-Zhe...
Phytochemical studies on roots of Morinda elliptica have resulted in the isolation of a new anthraqu...
Fig. 2. Key HMBC (A) and ROESY (B) correlations for compound 1.Published as part of Cao, Dong-Hua, L...
Fig. 2. Key HMBC correlations for 1, 4, and 6.Published as part of Zhao, Xiao-Tong, Yu, Mei-Hua, Su,...
Fig. 2. Key 1H–1H COSY () and HMBC () correlations of 1, 12 and 13.Published as part of Zhou, Xian-L...
Ekon JPL, Zra T, Songue JL, et al. New anthraquinone derivatives from the stem barks of Morinda luci...
Fig. 3. Key 1H–1H COSY (bold ─), and HMBC (→) correlations of compound 1 or 2; Key NOESY () correlat...
Fig. 2. Key HMBC correlations of compounds 1–10.Published as part of Xie, Jun, Wang, Hongqing, Dong,...
Fig. 2. Key HMBC correlations for compound 1.Published as part of Bendamene, Samia, Boutaghane, Naim...
Fig. 3. Key 1 H– 1 H COSY (blue arrows) and HMBC (red arrows) correlations in compounds 1 and 4. (Fo...
Fig. 1. Structures of compounds 1–4.Published as part of Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xie...
Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xie, Jun, Lai, Shengtian, Wang, Hongqing, Chen, Ruoyun, Kang...
Fig. 6. X-ray crystal structure of 4.Published as part of Li, Changkang, Dong, Chaoxuan, Fu, Jia, Xi...
Fig. 4. Experimental ECD spectra obtained in MeOH and calculated ECD spectra for isomers 1–4 (a–d, r...
Fig. 2. Chiral HPLC-UV chromatogram of racemic 1–4 (a–d) using a Chiralpak AD-H column (4.6 mm × 250...
Fig. 2. Key HMBC correlations of compound 1a/1b‒12.Published as part of Yin, Zhao-Kun, Liu, Zhao-Zhe...
Phytochemical studies on roots of Morinda elliptica have resulted in the isolation of a new anthraqu...
Fig. 2. Key HMBC (A) and ROESY (B) correlations for compound 1.Published as part of Cao, Dong-Hua, L...
Fig. 2. Key HMBC correlations for 1, 4, and 6.Published as part of Zhao, Xiao-Tong, Yu, Mei-Hua, Su,...
Fig. 2. Key 1H–1H COSY () and HMBC () correlations of 1, 12 and 13.Published as part of Zhou, Xian-L...
Ekon JPL, Zra T, Songue JL, et al. New anthraquinone derivatives from the stem barks of Morinda luci...
Fig. 3. Key 1H–1H COSY (bold ─), and HMBC (→) correlations of compound 1 or 2; Key NOESY () correlat...
Fig. 2. Key HMBC correlations of compounds 1–10.Published as part of Xie, Jun, Wang, Hongqing, Dong,...
Fig. 2. Key HMBC correlations for compound 1.Published as part of Bendamene, Samia, Boutaghane, Naim...
Fig. 3. Key 1 H– 1 H COSY (blue arrows) and HMBC (red arrows) correlations in compounds 1 and 4. (Fo...