14518990

Source:http://linkedlifedata.com/resource/pubmed/id/14518990

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002078, umls-concept:C0030230, umls-concept:C0772162, umls-concept:C1704241
pubmed:issue	40
pubmed:dateCreated	2003-10-1
pubmed:abstractText	Reactions of alkynes with arenes proceeded in the presence of dinuclear palladium complexes and trialkylboranes to yield alkyne hydroarylation products with high stereoselectivity. In the reactions of monosubstituted benzenes, meta and para products were formed in statistical ratios, while no ortho isomers were detected.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7503056
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Oct
pubmed:issn	0002-7863
pubmed:author	pubmed-author:InoueYoshioY, pubmed-author:MitsuboshiTomohiroT, pubmed-author:SetoguchiHiroyukiH, pubmed-author:TsukadaNaofumiN
pubmed:issnType	Print
pubmed:day	8
pubmed:volume	125
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	12102-3
pubmed:dateRevised	2008-1-17
pubmed:year	2003
pubmed:articleTitle	Stereoselective cis-addition of aromatic C-H bonds to alkynes catalyzed by dinuclear palladium complexes.
pubmed:affiliation	Department of Materials Chemistry, Graduate School of Engineering, Tohoku University, Sendai 980-8579, Japan. tsukuda@aporg.che.tohoku.ac.jp
pubmed:publicationType	Journal Article