Fig. 5. The overlaid experimental and calculated ECD spectra of compounds 1–3, 5–8, and 10–15.Published as part of Zhang, Hai-Xin, Si, Jin-Guang, Li, Jing-Rong, Yu, Meng, Qin, Ling-Ling, Zhao, Chen-Xu, Zhang, Tao & Zou, Zhong-Mei, 2023, Eudesmane type sesquiterpenes from the rhizomes of Atractylodes macrocephala and their bioactivities, pp. 1-13 in Phytochemistry (113545) 206 on page 7, DOI: 10.1016/j.phytochem.2022.113545, http://zenodo.org/record/823060
Fig. 7. Experimental ECD spectrum of 6 (black) compared with the calculated ECD spectra of 6 (red) a...
Fig. 6. The induced ECD spectra of 8 (upside: starting spectrum; downside: finally processed spectru...
Fig. 4. Experimental and calculated ECD spectra for 1 and 10.Published as part of Youn, Isoo, Han, K...
Fig. 4. Measured ECD and calculated ECD spectra of compounds 2–5 together with their stereoisomers.P...
Two new eudesmane-type sesquiterpenoids, eudesma-4(15),7(11)-dien-8α,12-ether (atractylenother, 1) a...
Fig. 3. Experimental and calculated ECD spectra for 1; experimental ECD spectrum for 2.Published as ...
Fig. 5. Comparisons of calculated and experimental ECD spectra of 7‒12.Published as part of Zang, Yi...
Fig. 4. Experimental and calculated ECD spectra for 3 (A) and 4 (B).Published as part of Zhang, Jun-...
Fig. 4. Comparisons of calculated and experimental ECD spectra of 1‒6.Published as part of Zang, Yi,...
Fig. 5. Experimental and calculated ECD spectra for compounds 1–6 in MeOH.Published as part of Xu, W...
Fig. 5. Experimental and calculated ECD spectra for 7–10.Published as part of Singha, Suriphon, Yotm...
Fig. 5. Experimental ECD spectrum of 5 (black) compared with the calculated ECD spectra of 5 (red) a...
Fig. 5. Experimental ECD spectra of 2 and 3.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Li...
Fig. 4. Experimental and calculated ECD spectra for 1–6.Published as part of Singha, Suriphon, Yotma...
Fig. 5. Experimental and calculated ECD spectra of 3 in CH3OH.Published as part of Pei, Yue-Hu, Zhan...
Fig. 7. Experimental ECD spectrum of 6 (black) compared with the calculated ECD spectra of 6 (red) a...
Fig. 6. The induced ECD spectra of 8 (upside: starting spectrum; downside: finally processed spectru...
Fig. 4. Experimental and calculated ECD spectra for 1 and 10.Published as part of Youn, Isoo, Han, K...
Fig. 4. Measured ECD and calculated ECD spectra of compounds 2–5 together with their stereoisomers.P...
Two new eudesmane-type sesquiterpenoids, eudesma-4(15),7(11)-dien-8α,12-ether (atractylenother, 1) a...
Fig. 3. Experimental and calculated ECD spectra for 1; experimental ECD spectrum for 2.Published as ...
Fig. 5. Comparisons of calculated and experimental ECD spectra of 7‒12.Published as part of Zang, Yi...
Fig. 4. Experimental and calculated ECD spectra for 3 (A) and 4 (B).Published as part of Zhang, Jun-...
Fig. 4. Comparisons of calculated and experimental ECD spectra of 1‒6.Published as part of Zang, Yi,...
Fig. 5. Experimental and calculated ECD spectra for compounds 1–6 in MeOH.Published as part of Xu, W...
Fig. 5. Experimental and calculated ECD spectra for 7–10.Published as part of Singha, Suriphon, Yotm...
Fig. 5. Experimental ECD spectrum of 5 (black) compared with the calculated ECD spectra of 5 (red) a...
Fig. 5. Experimental ECD spectra of 2 and 3.Published as part of Wei, Mengsha, Zhou, Peng, Huang, Li...
Fig. 4. Experimental and calculated ECD spectra for 1–6.Published as part of Singha, Suriphon, Yotma...
Fig. 5. Experimental and calculated ECD spectra of 3 in CH3OH.Published as part of Pei, Yue-Hu, Zhan...
Fig. 7. Experimental ECD spectrum of 6 (black) compared with the calculated ECD spectra of 6 (red) a...
Fig. 6. The induced ECD spectra of 8 (upside: starting spectrum; downside: finally processed spectru...
Fig. 4. Experimental and calculated ECD spectra for 1 and 10.Published as part of Youn, Isoo, Han, K...