Fig. 4. Comparison of the calculated vs experimental ECD spectra in MeOH for compound 5.Published as part of Zhai, Yi-Jie, Huo, Guang-Ming, Wei, Jing, Lin, Li-Bin, Zhang, Qiang, Li, Jian-Nan, Chen, Xin, Han, Wen-Bo & Gao, Jin-Ming, 2022, Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola, pp. 1-8 in Phytochemistry (112981) 193 on page 4, DOI: 10.1016/j.phytochem.2021.112981, http://zenodo.org/record/823457
Fig. 3. Experimental ECD spectrum (solid line, left axis) of 7 in acetonitrile and theoretical ECD s...
Fig. 6. Experimental and calculated ECD spectra for compounds 2–7 in MeOH.Published as part of Jin, ...
Fig. 4. Experiment ECD spectra of compounds 1 and 2.Published as part of Li, Qin, Chen, Chunmei, He,...
Fig. 6. Comparison of the calculated and experimental ECD spectra in MeOH for compound 6.Published a...
Fig. 7. Experimental ECD spectra in MeOH for 1 and 7.Published as part of Zhai, Yi-Jie, Huo, Guang-M...
Fig. 1. The structures of compounds 1–20.Published as part of Zhai, Yi-Jie, Huo, Guang-Ming, Wei, Ji...
Fig. 2. Key COSY and HMBC correlations of compounds 1–7.Published as part of Zhai, Yi-Jie, Huo, Guan...
Fig. 5. Preparation of acetomide derivative 6a.Published as part of Zhai, Yi-Jie, Huo, Guang-Ming, W...
Zhai, Yi-Jie, Huo, Guang-Ming, Wei, Jing, Lin, Li-Bin, Zhang, Qiang, Li, Jian-Nan, Chen, Xin, Han, W...
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).Publis...
Fig. 8. (A) The binding mode of 10 (yellow) in complex with mushroom tyrosinase. Hydrogen bonds inte...
Fig. 4. Comparing of experimental and calculated ECD spectra of (±)-1 in MeOH.Published as part of Z...
Fig. 4. Experimental and calculated ECD spectra for compounds 1, 4, and 7.Published as part of Lin, ...
Fig. 4. Experimental and calculated ECD spectra for compound 1 in MeOH.Published as part of Jin, Tia...
Fig. 5. Experimental ECDs and calculated ECDs for compounds 4–7.Published as part of Xian, Peng-Jie,...
Fig. 3. Experimental ECD spectrum (solid line, left axis) of 7 in acetonitrile and theoretical ECD s...
Fig. 6. Experimental and calculated ECD spectra for compounds 2–7 in MeOH.Published as part of Jin, ...
Fig. 4. Experiment ECD spectra of compounds 1 and 2.Published as part of Li, Qin, Chen, Chunmei, He,...
Fig. 6. Comparison of the calculated and experimental ECD spectra in MeOH for compound 6.Published a...
Fig. 7. Experimental ECD spectra in MeOH for 1 and 7.Published as part of Zhai, Yi-Jie, Huo, Guang-M...
Fig. 1. The structures of compounds 1–20.Published as part of Zhai, Yi-Jie, Huo, Guang-Ming, Wei, Ji...
Fig. 2. Key COSY and HMBC correlations of compounds 1–7.Published as part of Zhai, Yi-Jie, Huo, Guan...
Fig. 5. Preparation of acetomide derivative 6a.Published as part of Zhai, Yi-Jie, Huo, Guang-Ming, W...
Zhai, Yi-Jie, Huo, Guang-Ming, Wei, Jing, Lin, Li-Bin, Zhang, Qiang, Li, Jian-Nan, Chen, Xin, Han, W...
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).Publis...
Fig. 8. (A) The binding mode of 10 (yellow) in complex with mushroom tyrosinase. Hydrogen bonds inte...
Fig. 4. Comparing of experimental and calculated ECD spectra of (±)-1 in MeOH.Published as part of Z...
Fig. 4. Experimental and calculated ECD spectra for compounds 1, 4, and 7.Published as part of Lin, ...
Fig. 4. Experimental and calculated ECD spectra for compound 1 in MeOH.Published as part of Jin, Tia...
Fig. 5. Experimental ECDs and calculated ECDs for compounds 4–7.Published as part of Xian, Peng-Jie,...
Fig. 3. Experimental ECD spectrum (solid line, left axis) of 7 in acetonitrile and theoretical ECD s...
Fig. 6. Experimental and calculated ECD spectra for compounds 2–7 in MeOH.Published as part of Jin, ...
Fig. 4. Experiment ECD spectra of compounds 1 and 2.Published as part of Li, Qin, Chen, Chunmei, He,...