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- W2014098216 abstract "ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTOrganocopper-Lewis acid mediated 1,3-chirality transfer of acyclic .gamma.,.delta.-dioxygenated (E)-.alpha.,.beta.-enoates. Regio-, (E)-stereo-, and diastereoselective .alpha.-alkylation approaching 100% selectivityToshiro. Ibuka, Tomio. Nakao, Shinji. Nishii, and Yoshinori. YamamotoCite this: J. Am. Chem. Soc. 1986, 108, 23, 7420–7422Publication Date (Print):November 1, 1986Publication History Published online1 May 2002Published inissue 1 November 1986https://doi.org/10.1021/ja00283a054RIGHTS & PERMISSIONSArticle Views403Altmetric-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 PDF (438 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information Get e-Alerts" @default.
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- W2014098216 title "Organocopper-Lewis acid mediated 1,3-chirality transfer of acyclic .gamma.,.delta.-dioxygenated (E)-.alpha.,.beta.-enoates. Regio-, (E)-stereo-, and diastereoselective .alpha.-alkylation approaching 100% selectivity" @default.
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