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• W2952488900 abstract "ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTNew Reagent for Reductive Coupling of Carbonyl and Imine Compounds: Highly Reactive Manganese-Mediated Pinacol Coupling of Aryl Aldehydes, Aryl Ketones, and AldiminesReuben D. Rieke and Seung-Hoi KimView Author Information Department of Chemistry, University of NebraskaLincoln, Lincoln, Nebraska 68588-0304 Cite this: J. Org. Chem. 1998, 63, 15, 5235–5239Publication Date (Web):July 7, 1998Publication History Received21 October 1997Published online7 July 1998Published inissue 1 July 1998https://doi.org/10.1021/jo971942yCopyright © 1998 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1497Altmetric-Citations75LEARN 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 (66 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Aldehydes,Chemical reactions,Ketones,Metals,Transition metals Get e-Alerts" @default.
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• W2952488900 title "New Reagent for Reductive Coupling of Carbonyl and Imine Compounds: Highly Reactive Manganese-Mediated Pinacol Coupling of Aryl Aldehydes, Aryl Ketones, and Aldimines" @default.
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