Enantiomeric Resolution of (±)-Mandelic Acid by (1R,2S)-(–)-Ephedrine. An Organic Chemistry Laboratory Experiment Illustrating Stereoisomerism
2005; American Chemical Society; Volume: 82; Issue: 7 Linguagem: Inglês
10.1021/ed082p1040
ISSN1938-1328
AutoresMarsha R. Baar, Andrea L. Cerrone-Szakal,
Tópico(s)Various Chemistry Research Topics
ResumoADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTEnantiomeric Resolution of (±)-Mandelic Acid by (1R,2S)-(–)-Ephedrine. An Organic Chemistry Laboratory Experiment Illustrating StereoisomerismMarsha R. Baar and Andrea L. Cerrone-Szakal View Author Information Department of Chemistry, Muhlenberg College, Allentown, PA 18104Cite this: J. Chem. Educ. 2005, 82, 7, 1040Publication Date (Web):July 1, 2005Publication History Received3 August 2009Published online1 July 2005Published inissue 1 July 2005https://pubs.acs.org/doi/10.1021/ed082p1040https://doi.org/10.1021/ed082p1040research-articleACS PublicationsRequest reuse permissionsArticle Views1631Altmetric-Citations12LEARN 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:Amines,Organic chemistry,Pharmaceutics,Stereoisomerism,Transition temperature Get e-Alerts
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