17134302

Source:http://linkedlifedata.com/resource/pubmed/id/17134302

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039673, umls-concept:C0220781, umls-concept:C1883254
pubmed:issue	25
pubmed:dateCreated	2006-11-30
pubmed:abstractText	We report a gold-catalyzed benzannulation of 3-hydroxy-1,5-enynes to generate tetrahydronaphthalenes. This mild process proves to be an effective method to synthesize various metasubstituted aromatic rings in good yields. [reaction: see text]
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Gold, http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents, http://linkedlifedata.com/resource/pubmed/chemical/Tetrahydronaphthalenes
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1523-7060
pubmed:author	pubmed-author:BarriaultLouisL, pubmed-author:GriséChristiane MCM
pubmed:issnType	Print
pubmed:day	7
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5905-8
pubmed:meshHeading	pubmed-meshheading:17134302-Catalysis, pubmed-meshheading:17134302-Cyclization, pubmed-meshheading:17134302-Gold, pubmed-meshheading:17134302-Indicators and Reagents, pubmed-meshheading:17134302-Isomerism, pubmed-meshheading:17134302-Magnetic Resonance Spectroscopy, pubmed-meshheading:17134302-Tetrahydronaphthalenes
pubmed:year	2006
pubmed:articleTitle	Gold-catalyzed synthesis of substituted tetrahydronaphthalenes.
pubmed:affiliation	Center for Catalysis Research and Innovation, Department of Chemistry, 10 Marie Curie, University of Ottawa, Ottawa, Ontario, Canada K1N 6N5.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't