<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>69(Pt 4)</volume><submitter>Andersson PF</submitter><pubmed_abstract>The asymmetric unit of the title compound, C20H18O6 (systematic name: 1β,3β-dihy-droxy-2β-meth-oxyfuro[4',3',2':4,5,6]-18-norandrosta-8,11,13-triene-7,17-dione), a dihydro derivative of the fungal steroid viridin, contains two mol-ecules with similar conformations. The rings bearing the hy-droxy groups adopt boat conformations. The absolute structure was assigned based on the known chirality of a precursor compound. In the crystal, mol-ecules are linked by O-H⋯O hydrogen bonds, generating a three-dimensional network and weak C-H⋯O inter-actions consolidate the packing.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o467-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3629508</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The furan-osteroid viridiol.</pubmed_title><pmcid>PMC3629508</pmcid><pubmed_authors>Broberg A</pubmed_authors><pubmed_authors>Andersson PF</pubmed_authors><pubmed_authors>Lundberg D</pubmed_authors></additional><is_claimable>false</is_claimable><name>The furan-osteroid viridiol.</name><description>The asymmetric unit of the title compound, C20H18O6 (systematic name: 1β,3β-dihy-droxy-2β-meth-oxyfuro[4',3',2':4,5,6]-18-norandrosta-8,11,13-triene-7,17-dione), a dihydro derivative of the fungal steroid viridin, contains two mol-ecules with similar conformations. The rings bearing the hy-droxy groups adopt boat conformations. The absolute structure was assigned based on the known chirality of a precursor compound. In the crystal, mol-ecules are linked by O-H⋯O hydrogen bonds, generating a three-dimensional network and weak C-H⋯O inter-actions consolidate the packing.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Apr</publication><modification>2025-04-26T16:09:02.377Z</modification><creation>2019-03-27T01:07:34Z</creation></dates><accession>S-EPMC3629508</accession><cross_references><pubmed>23634026</pubmed><doi>10.1107/S1600536813005606</doi></cross_references></HashMap>