Fig. 8. 1H NMR Δδ values in ppm for the bis-S- and R-MTPA esters of 5 in S-R Methanol-d4.Published as part of Zang, Yi, Gong, Yihua, Chen, Xia, Wen, Huiling, Qi, Changxing, Chen, Chunmei, Liu, Junjun, Luo, Zengwei, Wang, Jianping, Zhu, Hucheng & Zhang, Yonghui, 2021, Piperazine-2,5-dione derivatives and an α-pyrone polyketide from Penicillium griseofulvum and their immunosuppression activity, pp. 1-8 in Phytochemistry (112708) 186 on page 5, DOI: 10.1016/j.phytochem.2021.112708, http://zenodo.org/record/825870
Fig. 6. (S) and (R)-MTPA esters of 6 and their 1H NMR chemical shift differences.Published as part o...
Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.Published as part of X...
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).Publis...
Fig. 7. DP4 probabilities of 13C NMR data for both diastereoisomers of 4; comparing of experimental ...
Fig. 4. Linear correlation between the experimental and calculated 13C NMR chemical shift of 1-A and...
Fig. 5. Key 1H–1H COSY, HMBC, NOESY, and ROESY correlations of compounds 2–5.Published as part of Za...
Fig. 1. Chemical structures of compounds 1–9.Published as part of Zang, Yi, Gong, Yihua, Chen, Xia, ...
Fig. 2. Key 1H–1H COSY, HMBC, NOESY, and 1H–15N HMBC correlations of compound 1.Published as part of...
Zang, Yi, Gong, Yihua, Chen, Xia, Wen, Huiling, Qi, Changxing, Chen, Chunmei, Liu, Junjun, Luo, Zeng...
Fig. 6. ECD spectra of compounds 2–4 and 6.Published as part of Zang, Yi, Gong, Yihua, Chen, Xia, We...
Fig. 5. Linear correlation between the experimental and calculated 13C NMR chemical shifts for 1A an...
Fig. 6. Linear regression analysis of calculated 13C NMR shifts of (1′S)-1 (right) and (1′R)-1 (left...
Fig. 3. Key NOESY correlations (H↔H) of compounds 1, 4, 5 and 6a.Published as part of Xu, Ke, Li, Ga...
Fig. 5. Linear correlation between experimental and calculated 13C NMR chemical shifts of 3 at the B...
Fig. 4. ΔδRS (δ- δ) values of (R)-MPA ester of 2 and (S)-MPA ester of 2.Published as part of Feng, L...
Fig. 6. (S) and (R)-MTPA esters of 6 and their 1H NMR chemical shift differences.Published as part o...
Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.Published as part of X...
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).Publis...
Fig. 7. DP4 probabilities of 13C NMR data for both diastereoisomers of 4; comparing of experimental ...
Fig. 4. Linear correlation between the experimental and calculated 13C NMR chemical shift of 1-A and...
Fig. 5. Key 1H–1H COSY, HMBC, NOESY, and ROESY correlations of compounds 2–5.Published as part of Za...
Fig. 1. Chemical structures of compounds 1–9.Published as part of Zang, Yi, Gong, Yihua, Chen, Xia, ...
Fig. 2. Key 1H–1H COSY, HMBC, NOESY, and 1H–15N HMBC correlations of compound 1.Published as part of...
Zang, Yi, Gong, Yihua, Chen, Xia, Wen, Huiling, Qi, Changxing, Chen, Chunmei, Liu, Junjun, Luo, Zeng...
Fig. 6. ECD spectra of compounds 2–4 and 6.Published as part of Zang, Yi, Gong, Yihua, Chen, Xia, We...
Fig. 5. Linear correlation between the experimental and calculated 13C NMR chemical shifts for 1A an...
Fig. 6. Linear regression analysis of calculated 13C NMR shifts of (1′S)-1 (right) and (1′R)-1 (left...
Fig. 3. Key NOESY correlations (H↔H) of compounds 1, 4, 5 and 6a.Published as part of Xu, Ke, Li, Ga...
Fig. 5. Linear correlation between experimental and calculated 13C NMR chemical shifts of 3 at the B...
Fig. 4. ΔδRS (δ- δ) values of (R)-MPA ester of 2 and (S)-MPA ester of 2.Published as part of Feng, L...
Fig. 6. (S) and (R)-MTPA esters of 6 and their 1H NMR chemical shift differences.Published as part o...
Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.Published as part of X...
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).Publis...