Matches in SemOpenAlex for { <https://semopenalex.org/work/W1971014553> ?p ?o ?g. }
Showing items 1 to 81 of
81
with 100 items per page.
- W1971014553 endingPage "4100" @default.
- W1971014553 startingPage "4097" @default.
- W1971014553 abstract "ADVERTISEMENT RETURN TO ISSUEPREVLetterNEXTA New Catalytic Cu(II)/Sparteine Oxidant System for β,β-Phenolic Couplings of Styrenyl Phenols: Synthesis of Carpanone and Unnatural AnalogsR. Nathan Daniels, Olugbeminiyi O. Fadeyi, and Craig W. LindsleyView Author Information Departments of Chemistry and Pharmacology, Institute of Chemical Biology, Vanderbilt University, Nashville, Tennessee 37232[email protected]Cite this: Org. Lett. 2008, 10, 18, 4097–4100Publication Date (Web):August 27, 2008Publication History Received18 July 2008Published online27 August 2008Published inissue 18 September 2008https://doi.org/10.1021/ol801643tCopyright © 2008 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1674Altmetric-Citations21LEARN 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 (180 KB) Get e-AlertsSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Aromatic compounds,Coupling reactions,Hydrocarbons,Ligands,Molecular structure Get e-Alerts" @default.
- W1971014553 created "2016-06-24" @default.
- W1971014553 creator A5032673796 @default.
- W1971014553 creator A5037325947 @default.
- W1971014553 creator A5060483072 @default.
- W1971014553 date "2008-08-27" @default.
- W1971014553 modified "2023-09-23" @default.
- W1971014553 title "A New Catalytic Cu(II)/Sparteine Oxidant System for β,β-Phenolic Couplings of Styrenyl Phenols: Synthesis of Carpanone and Unnatural Analogs" @default.
- W1971014553 cites W11703586 @default.
- W1971014553 cites W1970910370 @default.
- W1971014553 cites W1975866911 @default.
- W1971014553 cites W2014579414 @default.
- W1971014553 cites W2045316977 @default.
- W1971014553 cites W2046583902 @default.
- W1971014553 cites W2050095094 @default.
- W1971014553 cites W2058628645 @default.
- W1971014553 cites W2076834356 @default.
- W1971014553 cites W2087429567 @default.
- W1971014553 cites W2315142891 @default.
- W1971014553 cites W2318715949 @default.
- W1971014553 cites W2952764902 @default.
- W1971014553 doi "https://doi.org/10.1021/ol801643t" @default.
- W1971014553 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18729467" @default.
- W1971014553 hasPublicationYear "2008" @default.
- W1971014553 type Work @default.
- W1971014553 sameAs 1971014553 @default.
- W1971014553 citedByCount "21" @default.
- W1971014553 countsByYear W19710145532012 @default.
- W1971014553 countsByYear W19710145532013 @default.
- W1971014553 countsByYear W19710145532014 @default.
- W1971014553 countsByYear W19710145532015 @default.
- W1971014553 countsByYear W19710145532018 @default.
- W1971014553 countsByYear W19710145532019 @default.
- W1971014553 countsByYear W19710145532020 @default.
- W1971014553 countsByYear W19710145532021 @default.
- W1971014553 countsByYear W19710145532022 @default.
- W1971014553 countsByYear W19710145532023 @default.
- W1971014553 crossrefType "journal-article" @default.
- W1971014553 hasAuthorship W1971014553A5032673796 @default.
- W1971014553 hasAuthorship W1971014553A5037325947 @default.
- W1971014553 hasAuthorship W1971014553A5060483072 @default.
- W1971014553 hasConcept C136764020 @default.
- W1971014553 hasConcept C161191863 @default.
- W1971014553 hasConcept C161790260 @default.
- W1971014553 hasConcept C178790620 @default.
- W1971014553 hasConcept C185592680 @default.
- W1971014553 hasConcept C2777728882 @default.
- W1971014553 hasConcept C2778805511 @default.
- W1971014553 hasConcept C41008148 @default.
- W1971014553 hasConcept C518677369 @default.
- W1971014553 hasConceptScore W1971014553C136764020 @default.
- W1971014553 hasConceptScore W1971014553C161191863 @default.
- W1971014553 hasConceptScore W1971014553C161790260 @default.
- W1971014553 hasConceptScore W1971014553C178790620 @default.
- W1971014553 hasConceptScore W1971014553C185592680 @default.
- W1971014553 hasConceptScore W1971014553C2777728882 @default.
- W1971014553 hasConceptScore W1971014553C2778805511 @default.
- W1971014553 hasConceptScore W1971014553C41008148 @default.
- W1971014553 hasConceptScore W1971014553C518677369 @default.
- W1971014553 hasIssue "18" @default.
- W1971014553 hasLocation W19710145531 @default.
- W1971014553 hasLocation W19710145532 @default.
- W1971014553 hasOpenAccess W1971014553 @default.
- W1971014553 hasPrimaryLocation W19710145531 @default.
- W1971014553 hasRelatedWork W1990385249 @default.
- W1971014553 hasRelatedWork W2062327475 @default.
- W1971014553 hasRelatedWork W2396723359 @default.
- W1971014553 hasRelatedWork W2748952813 @default.
- W1971014553 hasRelatedWork W2899084033 @default.
- W1971014553 hasRelatedWork W2949395137 @default.
- W1971014553 hasRelatedWork W2949537469 @default.
- W1971014553 hasRelatedWork W2950168212 @default.
- W1971014553 hasRelatedWork W2951803252 @default.
- W1971014553 hasRelatedWork W4252524260 @default.
- W1971014553 hasVolume "10" @default.
- W1971014553 isParatext "false" @default.
- W1971014553 isRetracted "false" @default.
- W1971014553 magId "1971014553" @default.
- W1971014553 workType "article" @default.