羟醛反应
伊萨丁
立体选择性
化学
羟醛缩合
有机化学
催化作用
作者
J. Michael Ellis,Larry E. Overman,Huw R. Tanner,Jocelyn Wang
摘要
ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTA Versatile Synthesis of Unsymmetrical 3,3′-Bioxindoles: Stereoselective Mukaiyama Aldol Reactions of 2-Siloxyindoles with IsatinsJ. Michael Ellis, Larry E. Overman*, Huw R. Tanner, and Jocelyn WangView Author Information Department of Chemistry, 1102 Natural Sciences II, University of California, Irvine, California 92697-2025[email protected]Cite this: J. Org. Chem. 2008, 73, 22, 9151–9154Publication Date (Web):October 15, 2008Publication History Received22 August 2008Published online15 October 2008Published inissue 21 November 2008https://pubs.acs.org/doi/10.1021/jo801867whttps://doi.org/10.1021/jo801867wbrief-reportACS PublicationsCopyright © 2008 American Chemical SocietyRequest reuse permissionsArticle Views4152Altmetric-Citations27LEARN 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 (3)»Supporting Information Supporting Information SUBJECTS:Adducts,Aldol reactions,Oxindoles,Stereoselectivity,Substituents Get e-Alerts
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