12120380

Source:http://linkedlifedata.com/resource/pubmed/id/12120380

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016850, umls-concept:C0439836, umls-concept:C0439851, umls-concept:C1552596, umls-concept:C1947931
pubmed:issue	3
pubmed:dateCreated	2002-7-17
pubmed:abstractText	The first calixhetarenes with more than one heteroatom in the constituent rings are prepared in one step by treatment of calix[4]furan 1a and calix[6]furan 1b with ethyl carbamate, thionyl chloride and pyridine to give 2, 3, 4 and 5, 6, 7 respectively; these products have been characterised by X-ray crystallography which reveals that in 2 all eight heteroatoms lie on one face of the macrocyle.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Feb
pubmed:issn	1359-7345
pubmed:author	pubmed-author:GuillardJérômeJ, pubmed-author:Meth-CohnOttoO, pubmed-author:ReesCharles WCW, pubmed-author:WhiteAndrew J PAJ, pubmed-author:WilliamsDavid JDJ
pubmed:issnType	Print
pubmed:day	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	232-3
pubmed:dateRevised	2003-11-3
pubmed:year	2002
pubmed:articleTitle	Direct conversion of macrocyclic furans into macrocyclic isothiazoles.
pubmed:affiliation	Chemistry Department, University of Sunderland, Sunderland, UK SR1 3SD.
pubmed:publicationType	Journal Article