Tandem Aldol−Tishchenko Reactions of Lithium Enolates: A Highly Stereoselective Method for Diol and Triol Synthesis

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTTandem Aldol−Tishchenko Reactions of Lithium Enolates: A Highly Stereoselective Method for Diol and Triol SynthesisPaul M. Bodnar, Jared T. Shaw, and K. A. WoerpelView Author Information Department of Chemistry, University of California, Irvine, California 92697-2025Cite this: J. Org. Chem. 1997, 62, 17, 5674–5675Publication Date (Web):August 22, 1997Publication History Received6 June 1997Published online22 August 1997Published inissue 1 August 1997https://pubs.acs.org/doi/10.1021/jo971012ehttps://doi.org/10.1021/jo971012erapid-communicationACS PublicationsCopyright © 1997 American Chemical SocietyRequest reuse permissionsArticle Views1757Altmetric-Citations74LEARN 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 InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Aldehydes,Aldol reactions,Enolates,Lithium,Transfer reactions Get e-Alerts