12054980

Source:http://linkedlifedata.com/resource/pubmed/id/12054980

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0598128, umls-concept:C1883254
pubmed:issue	12
pubmed:dateCreated	2002-6-10
pubmed:abstractText	Treatment of furoisoxazolidines with NaH leads to functionalized 3-amino-2(5H)-furanones through a new rearrangement pattern of the isoxazolidine nucleus. This process has been usefully exploited for the synthesis of enantiomerically pure (5R)-3-alkylamino-5-methyl-2(5H)-furanones.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jun
pubmed:issn	0022-3263
pubmed:author	pubmed-author:ChiacchioUgoU, pubmed-author:CorsaroAntoninoA, pubmed-author:IannazzoDanielaD, pubmed-author:PipernoAnnaA, pubmed-author:ProcopioAntonioA, pubmed-author:RescifinaAntonioA, pubmed-author:RomeoGiovanniG, pubmed-author:RomeoRobertoR
pubmed:issnType	Print
pubmed:day	14
pubmed:volume	67
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4380-3
pubmed:dateRevised	2003-11-3
pubmed:year	2002
pubmed:articleTitle	Intramolecular cycloadditions of alpha-allyloxycarbonylnitrones: stereoselective synthesis of 3-amino-2(5H)furanones.
pubmed:affiliation	Dipartimento di Scienze Chimiche, Università di Catania, Viale Andrea Doria 6, 95125, Italy. uchiacchio@dipchi.unict.it
pubmed:publicationType	Journal Article