<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>73(Pt 8)</volume><submitter>Donkeng Dazie J</submitter><pubmed_abstract>The asymmetric unit of the title compound, C12H15NO, comprises two sym-metry-independent mol-ecules which differ mainly in the conformations of the tert-butyl groups. The mol-ecules contain an essentially planar five-membered 3-pyrroline ring incorporating a carbonyl substituent (pyrrolinone) which forms part of an isoindolinone skeleton. The planarity of the pyrrole ring is compared to other structures with isoindolinone. There are only weak intra- and inter-molecular C-H?O and C-H??-electron-ring inter-actions in the crystal structure.</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>1184-1188</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5598845</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure of 2-tert-butyl-2,3-di-hydro-1H-benzo[c]pyrrol-1-one.</pubmed_title><pmcid>PMC5598845</pmcid><pubmed_authors>Ludvik J</pubmed_authors><pubmed_authors>Donkeng Dazie J</pubmed_authors><pubmed_authors>Fabry J</pubmed_authors><pubmed_authors>Eigner V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure of 2-tert-butyl-2,3-di-hydro-1H-benzo[c]pyrrol-1-one.</name><description>The asymmetric unit of the title compound, C12H15NO, comprises two sym-metry-independent mol-ecules which differ mainly in the conformations of the tert-butyl groups. The mol-ecules contain an essentially planar five-membered 3-pyrroline ring incorporating a carbonyl substituent (pyrrolinone) which forms part of an isoindolinone skeleton. The planarity of the pyrrole ring is compared to other structures with isoindolinone. There are only weak intra- and inter-molecular C-H?O and C-H??-electron-ring inter-actions in the crystal structure.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jul</publication><modification>2021-02-20T10:10:56Z</modification><creation>2019-03-27T02:56:22Z</creation></dates><accession>S-EPMC5598845</accession><cross_references><pubmed>28932433</pubmed><doi>10.1107/S2056989017010337</doi></cross_references></HashMap>