17328552

Source:http://linkedlifedata.com/resource/pubmed/id/17328552

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016850, umls-concept:C0043481, umls-concept:C0220781, umls-concept:C1883254, umls-concept:C2348236
pubmed:issue	7
pubmed:dateCreated	2007-3-22
pubmed:abstractText	[structure: see text]. 5-Endo-dig cycloisomerization of 1,4-di- and 1,2,4-trisubstituted but-3-yn-1-ones in the presence of a catalytic amount of zinc chloride (10 mol %) in dichloromethane at room temperature (22 degrees C) provides 2,5-di- and 2,3,5-trisubstituted furans in high yields (85-97%).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Mar
pubmed:issn	1523-7060
pubmed:author	pubmed-author:DembinskiRomanR, pubmed-author:DurhamAudreyA, pubmed-author:MorrealeMarco SMS, pubmed-author:SniadyAdamA, pubmed-author:WheelerKraig AKA
pubmed:issnType	Print
pubmed:day	29
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1175-8
pubmed:year	2007
pubmed:articleTitle	Room temperature zinc chloride-catalyzed cycloisomerization of Alk-3-yn-1-ones: synthesis of substituted furans.
pubmed:affiliation	Department of Chemistry, Oakland University, Rochester, MI 48309-4477, USA.
pubmed:publicationType	Journal Article