Fig. 2. Key 1H-1H COSY (bold bonds) and HMBC (blue arrows) correlations of 1–4. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)Published as part of M, Benjamin, etoyer, Benatrehina, Annecie, Rakotondraibe, L. Harinantenaina, Thouvenot, Louis, Asakawa, Yoshinori, Nour, Mohammed & Raharivelomanana, Phila, 2020, Dimeric and esterified sesquiterpenes from the liverwort Chiastocaulon caledonicum, pp. 1-8 in Phytochemistry (112495) 179 on page 3, DOI: 10.1016/j.phytochem.2020.112495, http://zenodo.org/record/829336
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key 1 H– 1 H COSY (blue arrows) and HMBC (red arrows) correlations in compounds 1 and 4. (Fo...
Fig. 5. Key 1H-1H COSY (bold bonds) and HMBC (blue arrows) correlations for 6 and 7. (For interpreta...
Fig. 4. Key 1H-1H COSY (bold bonds), HMBC (blue arrows), and NOE correlations (red arrows) for compo...
Fig. 3. Key NOE correlations of 1–4.Published as part of M, Benjamin, etoyer, Benatrehina, Annecie, ...
Fig. 6. Key NOE correlations for compounds 6 and 7.Published as part of M, Benjamin, etoyer, Benatre...
Fig. 1. Isolated compounds from C. caledonicum.Published as part of M, Benjamin, etoyer, Benatrehina...
M, Benjamin, etoyer, Benatrehina, Annecie, Rakotondraibe, L. Harinantenaina, Thouvenot, Louis, Asaka...
Fig. 7. Proposed biosynthesis for the chiastocaulin structure.Published as part of M, Benjamin, etoy...
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key 1H 1H COSY (red) and HMBC correlations (blue) of compounds 1–11. (For interpretation of ...
Fig. 3. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–6.Published as part of Kang, Xin, Yan...
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key 1 H– 1 H COSY (blue arrows) and HMBC (red arrows) correlations in compounds 1 and 4. (Fo...
Fig. 5. Key 1H-1H COSY (bold bonds) and HMBC (blue arrows) correlations for 6 and 7. (For interpreta...
Fig. 4. Key 1H-1H COSY (bold bonds), HMBC (blue arrows), and NOE correlations (red arrows) for compo...
Fig. 3. Key NOE correlations of 1–4.Published as part of M, Benjamin, etoyer, Benatrehina, Annecie, ...
Fig. 6. Key NOE correlations for compounds 6 and 7.Published as part of M, Benjamin, etoyer, Benatre...
Fig. 1. Isolated compounds from C. caledonicum.Published as part of M, Benjamin, etoyer, Benatrehina...
M, Benjamin, etoyer, Benatrehina, Annecie, Rakotondraibe, L. Harinantenaina, Thouvenot, Louis, Asaka...
Fig. 7. Proposed biosynthesis for the chiastocaulin structure.Published as part of M, Benjamin, etoy...
Fig. 2. Key 1H-1 H COSY (red bold), HMBC (solid arrows) and key ROESY correlations (dashed arrows) o...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 2. Key 1H 1H COSY (red) and HMBC correlations (blue) of compounds 1–11. (For interpretation of ...
Fig. 3. Key 1 H– 1 H COSY and HMBC correlations of compounds 1–6.Published as part of Kang, Xin, Yan...
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) corr...
Fig. 3. Key 1 H– 1 H COSY (blue arrows) and HMBC (red arrows) correlations in compounds 1 and 4. (Fo...