<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-18T23:54:18Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/14028" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/14028</identifier><datestamp>2026-10-18T21:14:21Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Crystal structure and Hirshfeld surface analysis of 2-oxo-13-epi-manoyl oxide isolated from Sideritis perfoliata</dc:title><dc:creator>Çelik, Ísmail</dc:creator><dc:creator>Atioǧlu, Zeliha</dc:creator><dc:creator>Aksit, Huseyin</dc:creator><dc:creator>Demirtas, Ibrahim</dc:creator><dc:creator>Erenler, Ramazan</dc:creator><dc:creator>Akkurt, Mehmet</dc:creator><dc:subject>crystal structure</dc:subject><dc:subject>cyclohexane rings</dc:subject><dc:subject>helical supramolecular chains</dc:subject><dc:subject>Hirshfeld surface analysis</dc:subject><dc:subject>tetrahydropyran rings</dc:subject><dc:description>The title compound, C20 H32 O2 (systematic name: 3-ethenyl-3,4a,7,7,10a-pentamethyldodecahydro-9H-benzo[f]chromen-9-one), was isolated from Sideritis perfoliata. In the crystal, molecules pack in helical supramolecular chains along the 2 1 screw axis running parallel to the a axis, bound by C - H...O hydrogen bonds. These chains are efficiently interlocked in the other two unit-cell directions via van der Waals interactions. Hirshfeld surface analysis shows that van der Waals interactions constitute the major contribution to the intermolecular interactions, with H...H contacts accounting for 86.0% of the surface. © Çelik et al. 2018.</dc:description><dc:publisher>International Union of Crystallography</dc:publisher><dc:date>2018</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/14028</dc:identifier><dc:identifier>https://doi.org/10.1107/s2056989018005807</dc:identifier><dc:identifier>2056-9890</dc:identifier><dc:language>en</dc:language><dc:relation>Acta Crystallographica Section E: Crystallographic Communications</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/14028</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>