Stereoselective Transformation of Enantiopure Cyclohexenol into cis-Hydrindan. An Enantioselective Formal Total Synthetic Route to (+)-Pumiliotoxin C

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTStereoselective Transformation of Enantiopure Cyclohexenol into cis-Hydrindan. An Enantioselective Formal Total Synthetic Route to (+)-Pumiliotoxin CMasahiro Toyota, Takanobu Asoh, Masaki Matsuura, and Keiichiro FukumotoView Author Information Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-77, Japan Cite this: J. Org. Chem. 1996, 61, 24, 8687–8691Publication Date (Web):November 29, 1996Publication History Received10 July 1996Published online29 November 1996Published inissue 1 January 1996https://doi.org/10.1021/jo9613085Copyright © 1996 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1272Altmetric-Citations39LEARN 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 (200 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Anions,Chemical synthesis,Cyclization,Organic compounds,Organic synthesis Get e-Alerts