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pubmed-article:14748580rdf:typepubmed:Citationlld:pubmed
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pubmed-article:14748580pubmed:dateCreated2004-1-29lld:pubmed
pubmed-article:14748580pubmed:abstractText[structure: see text] We have prepared 7,9-diazabicyclo[4.2.2]dec-3-ene-8,10-dione (3) and 7,9-diazabicyclo[4.2.2]decane-8,10-dione (4), which differ by virtue of the degree of unsaturation in the bridging carbacyclic tether on a 2,5-diketopiperazine. Remarkably different self-assembly patterns were observed in the solid state for the two compounds, attributed to subtle variations in the conformational constraints imposed by the tether.lld:pubmed
pubmed-article:14748580pubmed:languageenglld:pubmed
pubmed-article:14748580pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:14748580pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:14748580pubmed:monthFeblld:pubmed
pubmed-article:14748580pubmed:issn1523-7060lld:pubmed
pubmed-article:14748580pubmed:authorpubmed-author:ToungeBrett...lld:pubmed
pubmed-article:14748580pubmed:authorpubmed-author:DuYanmingYlld:pubmed
pubmed-article:14748580pubmed:authorpubmed-author:ReitzAllen...lld:pubmed
pubmed-article:14748580pubmed:authorpubmed-author:CreightonChri...lld:pubmed
pubmed-article:14748580pubmed:issnTypePrintlld:pubmed
pubmed-article:14748580pubmed:day5lld:pubmed
pubmed-article:14748580pubmed:volume6lld:pubmed
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pubmed-article:14748580pubmed:pagination309-12lld:pubmed
pubmed-article:14748580pubmed:year2004lld:pubmed
pubmed-article:14748580pubmed:articleTitleNoncovalent self-assembly of bicyclo[4.2.2]diketopiperazines: influence of saturation in the bridging carbacyclic ring.lld:pubmed
pubmed-article:14748580pubmed:affiliationDrug Discovery Division, Johnson & Johnson Pharmaceutical Research and Development, Spring House, Pennsylvania 19477, USA.lld:pubmed
pubmed-article:14748580pubmed:publicationTypeJournal Articlelld:pubmed