15387550

Source:http://linkedlifedata.com/resource/pubmed/id/15387550

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0000967, umls-concept:C0002078, umls-concept:C0220781, umls-concept:C0770014, umls-concept:C1883254
pubmed:issue	20
pubmed:dateCreated	2004-9-24
pubmed:abstractText	[reaction: see text] Substituted cyclopentadienone acetals (CPDAs) were synthesized by a thermal or palladium-catalyzed [3 + 2] cycloaddition reaction of a substituted cyclopropenone acetal to an electron-deficient acetylene. The synthesis afforded di-, tri-, and tetra-substituted CPDAs of considerable structural varieties that undergo Diels-Alder reaction to produce bicyclo[2.2.1]heptenes.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Sep
pubmed:issn	1523-7060
pubmed:author	pubmed-author:IsobeHiroyukiH, pubmed-author:NakamuraEiichiE, pubmed-author:SokJ EJE, pubmed-author:TanakaTakatsuguT, pubmed-author:TokuyamaHidetoshiH
pubmed:issnType	Print
pubmed:day	30
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3569-71
pubmed:year	2004
pubmed:articleTitle	Thermal and palladium-catalyzed [3 + 2] synthesis of cyclopentadienone acetals from cyclopropenone acetals and acetylenes.
pubmed:affiliation	Department of Chemistry, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
pubmed:publicationType	Journal Article