15357620

Source:http://linkedlifedata.com/resource/pubmed/id/15357620

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002505, umls-concept:C0006222, umls-concept:C0023688, umls-concept:C0030230, umls-concept:C0037638, umls-concept:C0439855, umls-concept:C0443286, umls-concept:C1704689, umls-concept:C1880497, umls-concept:C1996904, umls-concept:C2348236
pubmed:issue	19
pubmed:dateCreated	2004-9-10
pubmed:abstractText	An air- and moisture-stable (pi-allyl)palladium complex bearing a unique diphosphinidenecyclobutene ligand effectively catalyzes amination reactions of aryl bromides with amines, where the reactions proceed under mild conditions without solvent, with 2 mol % of catalyst and 1 equiv of t-BuOK at room temperature. Under these conditions the amination products were obtained in good to excellent isolated yields.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Sep
pubmed:issn	0022-3263
pubmed:author	pubmed-author:GajareAnil SAS, pubmed-author:OzawaFumiyukiF, pubmed-author:ToyotaKozoK, pubmed-author:YoshifujiMasaakiM
pubmed:issnType	Print
pubmed:day	17
pubmed:volume	69
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	6504-6
pubmed:year	2004
pubmed:articleTitle	Solvent free amination reactions of aryl bromides at room temperature catalyzed by a (pi-allyl)palladium complex bearing a diphosphinidenecyclobutene ligand.
pubmed:affiliation	Department of Chemistry, Graduate School of Science, Tohoku University, Aoba, Sendai 980-8578, Japan.
pubmed:publicationType	Journal Article