Enantioselective Biomimetic Transamination of β-Keto Carboxylic Acid Derivatives. An Efficient Asymmetric Synthesis of β-(Fluoroalkyl) β-Amino Acids

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTEnantioselective Biomimetic Transamination of β-Keto Carboxylic Acid Derivatives. An Efficient Asymmetric Synthesis of β-(Fluoroalkyl) β-Amino AcidsVadim A. Soloshonok, Taizo Ono, and Irina V. SoloshonokView Author Information National Industrial Research Institute of Nagoya, Hirate-cho 1-1, Kita-ku, Nagoya City, Aichi Prefecture 462, Japan Cite this: J. Org. Chem. 1997, 62, 22, 7538–7539Publication Date (Web):October 31, 1997Publication History Received9 June 1997Published online31 October 1997Published inissue 1 October 1997https://pubs.acs.org/doi/10.1021/jo9710238https://doi.org/10.1021/jo9710238rapid-communicationACS PublicationsCopyright © 1997 American Chemical SocietyRequest reuse permissionsArticle Views690Altmetric-Citations69LEARN 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-AlertscloseSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Biotechnology,Enantioselective synthesis,Isomerization,Organic compounds,Reaction products Get e-Alerts