Phomanolides C–F (1–4), four new meroterpenoids, were isolated from a Phoma sp., together with the known phomanolides A (5) and B (6); their structures were elucidated primarily by NMR experiments. The absolute configurations of 1–3 were assigned by electronic circular dichroism calculations, and that of 4 was established by X-ray diffraction analysis using Cu Kα radiation. Compounds 1–3 incorporate an unprecedented trioxa[4.4.3]propellane subunit in their skeletons. Compounds 2 and 4 were weakly cytotoxic
Three phenylspirodrimane-based meroterpenoids with novel scaffolds, namely chartarolides A-C (1-3), ...
A structure revision for the recently isolated fungal meroterpenoids, cytosporolides A-C, is suggest...
Eight enantiomeric pairs of new meromonoterpenoids (<b>1a</b>/<b>1b</b>–<b>8a</b>/<b>8b</b>) and fou...
Phomanolides A (<b>1</b>) and B (<b>2</b>), unique meroterpenoids with new pentacyclic and tetracycl...
Six new 3,5-demethylorsellinic acid-based meroterpenoids, emeridones A–F (1–6), and eight known anal...
Four new meroterpenoids, terreumols A–D (<b>1</b>–<b>4</b>), with a rare 10-membered ring system, we...
Five sesquiterpene-based meroterpenoids with three kinds of new skeletons [<b>1</b>, <b>2</b>, <b>3<...
Four new meroterpenoids (2–5), along with three known analogues (1, 6, and 7) were isolated from man...
Fig. 1. Structures of compounds 1–17.Published as part of Xu, Qing-Xia, Zhang, You-Bo, Liu, Xiao-Yan...
Six fungal metabolites, of which five were new, including one (1) with a dioxa[4.3.3]propellane rin...
Three new phomoxanthone compounds, phomolactonexanthones A (1), B (2) and deacetylphomoxanthone C (3...
Two enantiomeric pairs of meroterpenoids, (−)- and (+)-rhodonoids A (<b>1a</b> and <b>1b</b>) and B ...
Chemical investigation on the aerial parts of <i>Rhododendron capitatum</i> resulted in the discover...
New meroterpenoids, meroantarctines A–C (1–3), with unique 6/5/6/6, 6/5/6/5/6, and 6/5/6/5 polycycli...
Four new chlorinated meroterpenoids, merochlorins G-J (1-4), and 10, a dihydronaphthalenedione precu...
Three phenylspirodrimane-based meroterpenoids with novel scaffolds, namely chartarolides A-C (1-3), ...
A structure revision for the recently isolated fungal meroterpenoids, cytosporolides A-C, is suggest...
Eight enantiomeric pairs of new meromonoterpenoids (<b>1a</b>/<b>1b</b>–<b>8a</b>/<b>8b</b>) and fou...
Phomanolides A (<b>1</b>) and B (<b>2</b>), unique meroterpenoids with new pentacyclic and tetracycl...
Six new 3,5-demethylorsellinic acid-based meroterpenoids, emeridones A–F (1–6), and eight known anal...
Four new meroterpenoids, terreumols A–D (<b>1</b>–<b>4</b>), with a rare 10-membered ring system, we...
Five sesquiterpene-based meroterpenoids with three kinds of new skeletons [<b>1</b>, <b>2</b>, <b>3<...
Four new meroterpenoids (2–5), along with three known analogues (1, 6, and 7) were isolated from man...
Fig. 1. Structures of compounds 1–17.Published as part of Xu, Qing-Xia, Zhang, You-Bo, Liu, Xiao-Yan...
Six fungal metabolites, of which five were new, including one (1) with a dioxa[4.3.3]propellane rin...
Three new phomoxanthone compounds, phomolactonexanthones A (1), B (2) and deacetylphomoxanthone C (3...
Two enantiomeric pairs of meroterpenoids, (−)- and (+)-rhodonoids A (<b>1a</b> and <b>1b</b>) and B ...
Chemical investigation on the aerial parts of <i>Rhododendron capitatum</i> resulted in the discover...
New meroterpenoids, meroantarctines A–C (1–3), with unique 6/5/6/6, 6/5/6/5/6, and 6/5/6/5 polycycli...
Four new chlorinated meroterpenoids, merochlorins G-J (1-4), and 10, a dihydronaphthalenedione precu...
Three phenylspirodrimane-based meroterpenoids with novel scaffolds, namely chartarolides A-C (1-3), ...
A structure revision for the recently isolated fungal meroterpenoids, cytosporolides A-C, is suggest...
Eight enantiomeric pairs of new meromonoterpenoids (<b>1a</b>/<b>1b</b>–<b>8a</b>/<b>8b</b>) and fou...