Formation of Aziridine-2-amides through 5-Halo-6-methylperhydropyrimidin-4-ones. A Route to Enantiopure l - and d -Threonine andallo-Threonine

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTFormation of Aziridine-2-amides through 5-Halo-6-methylperhydropyrimidin-4-ones. A Route to Enantiopure l- and d-Threonine and allo-ThreonineGiuliana Cardillo, Luca Gentilucci, Alessandra Tolomelli, and Claudia TomasiniView Author Information Dipartimento di Chimica “G. Ciamician” and C.S.F.M., Università di Bologna, Via Selmi, 2-40126 Bologna, Italy Cite this: J. Org. Chem. 1998, 63, 10, 3458–3462Publication Date (Web):April 28, 1998Publication History Received28 July 1997Published online28 April 1998Published inissue 1 May 1998https://doi.org/10.1021/jo971388sCopyright © 1998 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views508Altmetric-Citations18LEARN 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 (148 KB) Get e-AlertsSUBJECTS:Adducts,Aziridines,Chemical reactions,Halogenation,Hydrolysis Get e-Alerts