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pubmed-article:10549145rdf:typepubmed:Citationlld:pubmed
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pubmed-article:10549145pubmed:issue9lld:pubmed
pubmed-article:10549145pubmed:dateCreated1999-11-23lld:pubmed
pubmed-article:10549145pubmed:abstractTextThe carbocyclic analogs of CMP, UMP, GMP, IMP, and ribo-TMP, of the same absolute configuration as the naturally occurring beta-D-ribofuranose-based ribonucleoside monophosphates, have been synthesized. The synthetic route employed Mitsunobu coupling of the heterocycles, appropriately protected where necessary, with a differentially protected, chiral carbocyclic core.lld:pubmed
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pubmed-article:10549145pubmed:authorpubmed-author:CaperelliC...lld:pubmed
pubmed-article:10549145pubmed:authorpubmed-author:AntleV DVDlld:pubmed
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pubmed-article:10549145pubmed:pagination1911-28lld:pubmed
pubmed-article:10549145pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:10549145pubmed:year1999lld:pubmed
pubmed-article:10549145pubmed:articleTitleSynthesis of chiral carbocyclic ribonucleotides.lld:pubmed
pubmed-article:10549145pubmed:affiliationDivision of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati Medical Center, OH 45267-0004, USA.lld:pubmed
pubmed-article:10549145pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10549145pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed