Nucleophilic Additions to 4,4-Disubstituted 2,5-Cyclohexadienones: Can Dipole Effects Control Facial Selectivity?
Citations Over TimeTop 13% of 1999 papers
Abstract
ADVERTISEMENT RETURN TO ISSUEPREVArticleNucleophilic Additions to 4,4-Disubstituted 2,5-Cyclohexadienones: Can Dipole Effects Control Facial Selectivity?Peter Wipf and Jae-Kyu JungView Author Information Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260 Cite this: Chem. Rev. 1999, 99, 5, 1469–1480Publication Date (Web):March 23, 1999Publication History Received19 August 1998Revised7 December 1998Published online23 March 1999Published inissue 12 May 1999https://pubs.acs.org/doi/10.1021/cr9803838https://doi.org/10.1021/cr9803838research-articleACS PublicationsCopyright © 1999 American Chemical SocietyRequest reuse permissionsArticle Views1314Altmetric-Citations50LEARN 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-Alertsclose SUBJECTS:Addition reactions,Carbonyls,Electrostatics,Polarity,Selectivity Get e-Alerts
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