Fig. 1. Structures of compounds 1–17.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang, Cheng-Cheng, Olga, Quasie, Yan, Dan, Tang, Peng-Fei, Zhang, Li-Na, Luo, Jun & Kong, Ling-Yi, 2020, Highly oxygenated and rearranged limonoids from the stem barks of Entandrophragma utile, pp. 1-10 in Phytochemistry (112282) 172 on page 2, DOI: 10.1016/j.phytochem.2020.112282, http://zenodo.org/record/829417
Fig. 4. Separated ORTEP-like view of the absolute configuration of 1 (A) and 3 (B), only asymmetric ...
Mouth, Gervais, Happi, e, Kemayou, Guy Paulin Mouthe, Stammler, Hans-Georg, Neumann, Beate, Ismail, ...
Fig. 1. Structures of limonoids 1–12.Published as part of Sun, Yujin, Cui, Letian, Sun, Yunpeng, Li,...
Fig. 4. X-ray crystallographic structure of 1.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang...
Hu, Ya-Lin, Tian, Xiao-Meng, Wang, Cheng-Cheng, Olga, Quasie, Yan, Dan, Tang, Peng-Fei, Zhang, Li-Na...
Fig. 6. Key HMBC and ROESY correlations of 4.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang,...
Fig. 7. Key HMBC and ROESY correlations of 10.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang,...
Fig. 8. The CD spectra of compounds 10–12 in MeOH; the bold lines denote the electric transition dip...
Fig. 5. The CD spectra of compounds 3–7 in MeOH; the bold lines denote the electric transition dipol...
Fig. 3. The CD spectrum of compound 1 in MeOH; the bold lines denote the electric transition dipole ...
Fig. 1. Chemical structures of compounds 1–5 isolated from E. candollei.Published as part of Mouth, ...
Fig. 3. ORTEP-like view of the asymmetric unit of the mixed crystal of compounds 1 + 3.Published as ...
Fig. 6. Structure and ORTEP-like view of scopoletin (6).Published as part of Mouth, Gervais, Happi, ...
Fig. 5. ORTEP-like view of compound 5. Only asymmtric carbon atoms were labelled, the absolute confi...
Fig. 4. Separated ORTEP-like view of the absolute configuration of 1 (A) and 3 (B), only asymmetric ...
Mouth, Gervais, Happi, e, Kemayou, Guy Paulin Mouthe, Stammler, Hans-Georg, Neumann, Beate, Ismail, ...
Fig. 1. Structures of limonoids 1–12.Published as part of Sun, Yujin, Cui, Letian, Sun, Yunpeng, Li,...
Fig. 4. X-ray crystallographic structure of 1.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang...
Hu, Ya-Lin, Tian, Xiao-Meng, Wang, Cheng-Cheng, Olga, Quasie, Yan, Dan, Tang, Peng-Fei, Zhang, Li-Na...
Fig. 6. Key HMBC and ROESY correlations of 4.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang,...
Fig. 7. Key HMBC and ROESY correlations of 10.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang...
Fig. 2. Key HMBC and ROESY correlations of 1.Published as part of Hu, Ya-Lin, Tian, Xiao-Meng, Wang,...
Fig. 8. The CD spectra of compounds 10–12 in MeOH; the bold lines denote the electric transition dip...
Fig. 5. The CD spectra of compounds 3–7 in MeOH; the bold lines denote the electric transition dipol...
Fig. 3. The CD spectrum of compound 1 in MeOH; the bold lines denote the electric transition dipole ...
Fig. 1. Chemical structures of compounds 1–5 isolated from E. candollei.Published as part of Mouth, ...
Fig. 3. ORTEP-like view of the asymmetric unit of the mixed crystal of compounds 1 + 3.Published as ...
Fig. 6. Structure and ORTEP-like view of scopoletin (6).Published as part of Mouth, Gervais, Happi, ...
Fig. 5. ORTEP-like view of compound 5. Only asymmtric carbon atoms were labelled, the absolute confi...
Fig. 4. Separated ORTEP-like view of the absolute configuration of 1 (A) and 3 (B), only asymmetric ...
Mouth, Gervais, Happi, e, Kemayou, Guy Paulin Mouthe, Stammler, Hans-Georg, Neumann, Beate, Ismail, ...
Fig. 1. Structures of limonoids 1–12.Published as part of Sun, Yujin, Cui, Letian, Sun, Yunpeng, Li,...