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pubmed-article:11126297rdf:typepubmed:Citationlld:pubmed
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pubmed-article:11126297pubmed:issue6lld:pubmed
pubmed-article:11126297pubmed:dateCreated2000-12-20lld:pubmed
pubmed-article:11126297pubmed:abstractTextA new tetrafluorophenol activated resin that facilitates the use of 19F NMR to quantitate loading is presented. This new resin provides a useful tool for acylation, and a novel activated polymeric sulfonate ester to generate sulfonamides. This activated resin reacts with a wide scope of N-nucleophiles including primary and secondary amines, and anilines. This new activated resin methodology provides a powerful tool for pure single-compound library synthesis.lld:pubmed
pubmed-article:11126297pubmed:languageenglld:pubmed
pubmed-article:11126297pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:11126297pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:11126297pubmed:issn1520-4766lld:pubmed
pubmed-article:11126297pubmed:authorpubmed-author:CrawfordKKlld:pubmed
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pubmed-article:11126297pubmed:pagination691-7lld:pubmed
pubmed-article:11126297pubmed:dateRevised2003-10-31lld:pubmed
pubmed-article:11126297pubmed:articleTitlePolymer-supported tetrafluorophenol: a new activated resin for chemical library synthesis.lld:pubmed
pubmed-article:11126297pubmed:affiliationLead Discovery Department, Rhone Poulen Rorer, Collegeville, Pennsylvania 19426, USA.lld:pubmed
pubmed-article:11126297pubmed:publicationTypeJournal Articlelld:pubmed