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- W2949572621 abstract "ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTNucleophilic Carbenes in Organic Synthesis. Construction of Functionalized Hydroindolones via a Novel Reaction Pathway of DimethoxycarbeneJames H. Rigby, Alexandre Cavezza, and Gulzar AhmedView Author Information Department of Chemistry, Wayne State University Detroit, Michigan 48202-3489 Cite this: J. Am. Chem. Soc. 1996, 118, 50, 12848–12849Publication Date (Web):December 18, 1996Publication History Received9 August 1996Published online18 December 1996Published inissue 1 January 1996https://doi.org/10.1021/ja962784fCopyright © 1996 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1117Altmetric-Citations49LEARN 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 (164 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Addition reactions,Carbene compounds,Cyclization,Organic compounds,Vinyl Get e-Alerts" @default.
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- W2949572621 title "Nucleophilic Carbenes in Organic Synthesis. Construction of Functionalized Hydroindolones <i>via</i> a Novel Reaction Pathway of Dimethoxycarbene" @default.
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