Fig. 2. (A) Selected 1H–1H COSY and HMBC correlations and (B) selected NOESY correlations for 7-deoxyiridolactonic acid (6) and linaburioside A (1).Published as part of Niwa, Kanji, Yi, Ren, Tanaka, Naonobu, Kitaguchi, Shindai, Tsuji, Daisuke, Kim, Sang-Yong, Tsogtbaatar, Ariuntuya, Bunddulam, Perleidulam, Kawazoe, Kazuyoshi, Kojoma, Mareshige, Damdinjav, Davaadagva, Itoh, Kohji & Kashiwada, Yoshiki, 2020, Linaburiosides A-D, acylated iridoid glucosides from Linaria buriatica, pp. 1-7 in Phytochemistry (112247) 171 on page 2, DOI: 10.1016/j.phytochem.2019.112247, http://zenodo.org/record/829386
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. Selected key HMBC () and 1H–1H COSY () correlations of compounds 1, 5, 7, 9a/9b, and 10a/10b...
Fig. 2. Key HMBC, COSY and ROESY correlations of compounds 1–11.Published as part of Mi, Cheng-neng,...
Fig. 1. Structures of linaburiosides A−D (1–4), iridolinarin C (5), and 7-deoxyiridolactonic acid (6...
Niwa, Kanji, Yi, Ren, Tanaka, Naonobu, Kitaguchi, Shindai, Tsuji, Daisuke, Kim, Sang-Yong, Tsogtbaat...
Fig. 3. Application of (A) the PGME method to 7-deoxyiridolactonic acid (6) and (B) modified Mosher'...
Fig. 2. Key HMBC and NOESY correlations of 1, 6, 7, 20, 22 and 24.Published as part of Xu, Hong-Tao,...
Fig. 2. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1 and 4.Pu...
Fig. 3. 1H–1H COSY and key HMBC (A), and selected NOESY (B) correlations of compounds 15–17.Publishe...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 4, 6, and 7.Published as part of Liu, H...
Fig. 2. Selected key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 6, 8, and 10.Published...
Fig. 4. Key NOESY correlations of compounds 2, 4, 5, and 7.Published as part of Zhou, Peng, Zheng, M...
Fig. 2. 1H–1H COSY and key HMBC correlations (A), selected NOESY correlations and nOe differences (B...
Fig. 2. 1H– 1H COSY correlations for compounds 6–10 and key HMBC correlations for compounds 1 and 6–...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. Selected key HMBC () and 1H–1H COSY () correlations of compounds 1, 5, 7, 9a/9b, and 10a/10b...
Fig. 2. Key HMBC, COSY and ROESY correlations of compounds 1–11.Published as part of Mi, Cheng-neng,...
Fig. 1. Structures of linaburiosides A−D (1–4), iridolinarin C (5), and 7-deoxyiridolactonic acid (6...
Niwa, Kanji, Yi, Ren, Tanaka, Naonobu, Kitaguchi, Shindai, Tsuji, Daisuke, Kim, Sang-Yong, Tsogtbaat...
Fig. 3. Application of (A) the PGME method to 7-deoxyiridolactonic acid (6) and (B) modified Mosher'...
Fig. 2. Key HMBC and NOESY correlations of 1, 6, 7, 20, 22 and 24.Published as part of Xu, Hong-Tao,...
Fig. 2. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1 and 4.Pu...
Fig. 3. 1H–1H COSY and key HMBC (A), and selected NOESY (B) correlations of compounds 15–17.Publishe...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 3, and 6.Published as part of Z...
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 4, 6, and 7.Published as part of Liu, H...
Fig. 2. Selected key 1H–1H COSY, HMBC, and NOESY correlations of compounds 1, 6, 8, and 10.Published...
Fig. 4. Key NOESY correlations of compounds 2, 4, 5, and 7.Published as part of Zhou, Peng, Zheng, M...
Fig. 2. 1H–1H COSY and key HMBC correlations (A), selected NOESY correlations and nOe differences (B...
Fig. 2. 1H– 1H COSY correlations for compounds 6–10 and key HMBC correlations for compounds 1 and 6–...
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.Published as part of Liu, Huan, Liu, Dan, Jia...
Fig. 2. Selected key HMBC () and 1H–1H COSY () correlations of compounds 1, 5, 7, 9a/9b, and 10a/10b...
Fig. 2. Key HMBC, COSY and ROESY correlations of compounds 1–11.Published as part of Mi, Cheng-neng,...