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- W2950363913 abstract "ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTThe Chemistry of Trichlorosilyl Enolates. 6. Mechanistic Duality in the Lewis Base-Catalyzed Aldol Addition ReactionScott E. Denmark, Xiping Su, and Yutaka NishigaichiView Author Information Roger Adams Laboratory, Department of Chemistry University of Illinois, Urbana, Illinois 61801 Cite this: J. Am. Chem. Soc. 1998, 120, 49, 12990–12991Publication Date (Web):December 1, 1998Publication History Received20 August 1998Published online1 December 1998Published inissue 1 December 1998https://doi.org/10.1021/ja982993vCopyright © 1998 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views962Altmetric-Citations65LEARN 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 (103 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Aldol reactions,Catalysts,Enolates,Molecular structure,Silicon Get e-Alerts" @default.
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- W2950363913 title "The Chemistry of Trichlorosilyl Enolates. 6. Mechanistic Duality in the Lewis Base-Catalyzed Aldol Addition Reaction" @default.
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