Control of the Enantiochemistry of Electrophilic Substitutions of N -Pivaloyl-α-lithio- o -ethylaniline: Stereoinformation Transfer Based on the Method of Organolithium Formation

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTControl of the Enantiochemistry of Electrophilic Substitutions of N-Pivaloyl-α-lithio-o-ethylaniline: Stereoinformation Transfer Based on the Method of Organolithium FormationAmit Basu and Peter BeakView Author Information Department of Chemistry, University of Illinois Urbana, Illinois 61801 Cite this: J. Am. Chem. Soc. 1996, 118, 6, 1575–1576Publication Date (Web):February 14, 1996Publication History Received12 June 1995Published online14 February 1996Published inissue 1 January 1996https://doi.org/10.1021/ja951895wCopyright © 1996 American Chemical SocietyRequest reuse permissionsArticle Views548Altmetric-Citations67LEARN 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 InReddit Read OnlinePDF (165 KB) Get e-AlertscloseSupporting Info (2)»Supporting Information Supporting Information SUBJECTS:Electrophiles,Molecular structure,Reagents,Stereoselectivity,Substitution reactions Get e-Alerts