2007
DOI: 10.1107/s1600536807024786
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Roridin H

Abstract: In the molecule of the title compound, C29H36O8, the five‐membered rings adopt envelope conformations, while the six‐membered rings have twist and chair conformations. The five‐membered rings also have pseudo‐mirror planes, while the six‐membered rings have pseudo‐twofold axes. In the crystal structure, intra‐ and intermolecular C—H...O hydrogen bonds cause the formation of a network structure. This study establishes the relative configuration of the compound.

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Cited by 2 publications
(1 citation statement)
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“…In 1999, the same group was able to employ insights from these X-ray studies in an investigation into the diastereomers of roridin E [ 110 ], following the work by Flippen-Anderson in 1986 [ 111 ], in order to infer the absolute configuration of various carbons in the sidechain, on the basis of 13 C NMR chemical shift differences near the stereogenic centers. The latest SCXRD work on the roridins was published by Gai in 2007 [ 112 ]. Here, the analysis of roridin H again focused on the stereochemistry of the sidechain, this time at positions C-4′, C-5′ and C-6′, which are part of a five-membered ring.…”
Section: Methods To Study Structurementioning
confidence: 99%
“…In 1999, the same group was able to employ insights from these X-ray studies in an investigation into the diastereomers of roridin E [ 110 ], following the work by Flippen-Anderson in 1986 [ 111 ], in order to infer the absolute configuration of various carbons in the sidechain, on the basis of 13 C NMR chemical shift differences near the stereogenic centers. The latest SCXRD work on the roridins was published by Gai in 2007 [ 112 ]. Here, the analysis of roridin H again focused on the stereochemistry of the sidechain, this time at positions C-4′, C-5′ and C-6′, which are part of a five-membered ring.…”
Section: Methods To Study Structurementioning
confidence: 99%