14961688

Source:http://linkedlifedata.com/resource/pubmed/id/14961688

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005899, umls-concept:C0220781, umls-concept:C0221821, umls-concept:C0439148, umls-concept:C1521991, umls-concept:C1524106, umls-concept:C1707689, umls-concept:C1883254
pubmed:issue	4
pubmed:dateCreated	2004-2-13
pubmed:abstractText	The design, synthesis and structural analysis of architecturally new cyclophanes (monomers, dimers, and trimers) are reported. Variable temperature NMR experiments reveal a regular, tandem dynamic in the cyclophane 2a that enables its description as a "molecular rocking chair". The NMR and X-ray structure investigations show important intra- and intermolecular aromatic pi-stacking interactions.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Feb
pubmed:issn	0022-3263
pubmed:author	pubmed-author:BalogMirelaM, pubmed-author:CondamineEricE, pubmed-author:GrosuIonI, pubmed-author:PléGérardG, pubmed-author:RamondencYvanY, pubmed-author:VargaRichard ARA
pubmed:issnType	Print
pubmed:day	20
pubmed:volume	69
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1337-45
pubmed:year	2004
pubmed:articleTitle	Design and synthesis of new macrocyclic cyclophanes using 1,3-dioxane units as bridges: a molecular "rocking chair".
pubmed:affiliation	Organic Chemistry Department and CSOFSTM, Babes-Bolyai University, Cluj-Napoca, Romania.
pubmed:publicationType	Journal Article