15387632

Source:http://linkedlifedata.com/resource/pubmed/id/15387632

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205198, umls-concept:C0522535, umls-concept:C0596311, umls-concept:C1330957, umls-concept:C1948027
pubmed:issue	20
pubmed:dateCreated	2004-9-24
pubmed:abstractText	Triarylmethanols are effectively dehydroarylated and reacted with some unsaturated compounds by using an appropriate palladium catalyst system such as Pd(OAc)2-P(1-Nap)3 (1-Nap = 1-naphthyl) to give the corresponding arenes and hydroarylation products, respectively, along with diaryl ketones.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Oct
pubmed:issn	0022-3263
pubmed:author	pubmed-author:MiuraMasahiroM, pubmed-author:NomotoMichiyoM, pubmed-author:NomuraMasakatsuM, pubmed-author:SatohTetsuyaT, pubmed-author:TeraoYoshitoY
pubmed:copyrightInfo	Copyright 2004 American Chemical Society
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	69
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	6942-4
pubmed:year	2004
pubmed:articleTitle	Palladium-catalyzed dehydroarylation of triarylmethanols and their coupling with unsaturated compounds accompanied by C-C bond cleavage.
pubmed:affiliation	Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.
pubmed:publicationType	Journal Article