Stereochemistry of a Cyclopropanone by Crystal Structure Analysis. The Exo Configuration of the Diels-Alder Adduct of Cyclopropenone and 1,3-Diphenylisobenzofuran Appears To Be Stabilized Relative to the Endo by an Attractive Ether-Carbonyl Interaction

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Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTStereochemistry of a Cyclopropanone by Crystal Structure Analysis. The Exo Configuration of the Diels-Alder Adduct of Cyclopropenone and 1,3-Diphenylisobenzofuran Appears To Be Stabilized Relative to the Endo by an Attractive Ether-Carbonyl InteractionMatthew H. J. Cordes, Susan de Gala, and Jerome A. BersonCite this: J. Am. Chem. Soc. 1994, 116, 24, 11161–11162Publication Date (Print):November 1, 1994Publication History Published online1 May 2002Published inissue 1 November 1994https://pubs.acs.org/doi/10.1021/ja00103a043https://doi.org/10.1021/ja00103a043research-articleACS PublicationsRequest reuse permissionsArticle Views237Altmetric-Citations21LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (2)»Supporting Information Supporting Information Get e-Alerts

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