<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>64(Pt 6)</volume><submitter>Svorc L</submitter><pubmed_abstract>The absolute configuration of the title compound, C(14)H(13)NO(2)S, was assigned from the synthesis and confirmed by the structure determination. The central six-membered ring of the indolizine system adopts an envelope conformation, the greatest deviation from the mean plane of the ring being 0.459 (2) Å for the N atom. The benzothieno system is planar [mean deviation = 0.009 (2) Å]. In the crystal structure, mol-ecules form chains parallel to the b axis via inter-molecular O-H⋯O hydrogen bonds.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o1164-5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2961476</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>(11R,11aS)-11-Hydr-oxy-1,5,11,11a-tetra-hydro-1-benzothieno[2,3-f]indolizin-3(2H)-one.</pubmed_title><pmcid>PMC2961476</pmcid><pubmed_authors>Kozisek J</pubmed_authors><pubmed_authors>Marchalin S</pubmed_authors><pubmed_authors>Svorc L</pubmed_authors><pubmed_authors>Vrabel V</pubmed_authors><pubmed_authors>Safar P</pubmed_authors></additional><is_claimable>false</is_claimable><name>(11R,11aS)-11-Hydr-oxy-1,5,11,11a-tetra-hydro-1-benzothieno[2,3-f]indolizin-3(2H)-one.</name><description>The absolute configuration of the title compound, C(14)H(13)NO(2)S, was assigned from the synthesis and confirmed by the structure determination. The central six-membered ring of the indolizine system adopts an envelope conformation, the greatest deviation from the mean plane of the ring being 0.459 (2) Å for the N atom. The benzothieno system is planar [mean deviation = 0.009 (2) Å]. In the crystal structure, mol-ecules form chains parallel to the b axis via inter-molecular O-H⋯O hydrogen bonds.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 May</publication><modification>2025-04-26T19:00:37.924Z</modification><creation>2019-03-27T00:00:00Z</creation></dates><accession>S-EPMC2961476</accession><cross_references><pubmed>21202672</pubmed><doi>10.1107/S1600536808015456</doi></cross_references></HashMap>