Practical Synthesis of 1,3-O-Di-tert-butylsilylene-Protected d - and l -Erythritols as a Four-Carbon Chiral Building Block

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTPractical Synthesis of 1,3-O-Di-tert-butylsilylene-Protected d- and l-Erythritols as a Four-Carbon Chiral Building BlockYuji Mori and Hisafumi HayashiView Author Information Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-ku, Nagoya 468-8503, Japan [email protected]Cite this: J. Org. Chem. 2001, 66, 25, 8666–8668Publication Date (Web):November 20, 2001Publication History Received13 July 2001Published online20 November 2001Published inissue 1 December 2001https://pubs.acs.org/doi/10.1021/jo0107103https://doi.org/10.1021/jo0107103brief-reportACS PublicationsCopyright © 2001 American Chemical SocietyRequest reuse permissionsArticle Views806Altmetric-Citations29LEARN 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-Alertsclose SUBJECTS:Alcohols,Mixtures,Molecular structure,Reaction products,Redox reactions Get e-Alerts