Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
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Résumé
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTAryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct ArylationDino Alberico, Mark E. Scott, and Mark LautensView Author Information Davenport Laboratories, Chemistry Department, University of Toronto, 80 St. George Street, Toronto, Ontario, Canada M5S 3H6 Cite this: Chem. Rev. 2007, 107, 1, 174–238Publication Date (Web):January 10, 2007Publication History Received6 July 2006Published online10 January 2007Published inissue 1 January 2007https://pubs.acs.org/doi/10.1021/cr0509760https://doi.org/10.1021/cr0509760research-articleACS PublicationsCopyright © 2007 American Chemical SocietyRequest reuse permissionsArticle Views36611Altmetric-Citations3415LEARN 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:Anions,Aromatic compounds,Arylation,Catalysts,Organic reactions Get e-Alerts
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La notice
- Revue
- Chemical Reviews
- Thématique
- Catalytic Cross-Coupling Reactions
- Domaine
- Chemistry
- Établissements canadiens
- University of Toronto
- Organismes subventionnaires
- —
- Mots-clés
- ArylCitationPower (physics)Social mediaChemistryComputer scienceLibrary scienceWorld Wide WebPhysicsOrganic chemistryThermodynamics
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