Dual Mechanisms of Acid-Catalyzed Rearrangement of Enol Ester Epoxides: Enantioselective Formation of α-Acyloxy Ketones

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTDual Mechanisms of Acid-Catalyzed Rearrangement of Enol Ester Epoxides: Enantioselective Formation of α-Acyloxy KetonesYuanming Zhu, Karl J. Manske, and Yian ShiView Author Information Department of Chemistry, Colorado State University Fort Collins, Colorado 80523 Cite this: J. Am. Chem. Soc. 1999, 121, 16, 4080–4081Publication Date (Web):April 8, 1999Publication History Received13 January 1999Published online8 April 1999Published inissue 1 April 1999https://doi.org/10.1021/ja990124fCopyright © 1999 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1229Altmetric-Citations36LEARN 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 (63 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Ethers,Ketones,Molecular structure,Organic compounds,Rearrangement Get e-Alerts