15575678

Source:http://linkedlifedata.com/resource/pubmed/id/15575678

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0060850, umls-concept:C0185125, umls-concept:C0220781, umls-concept:C0596514, umls-concept:C1883254
pubmed:issue	25
pubmed:dateCreated	2004-12-3
pubmed:abstractText	[reaction: see text] A catalyst generated from Pd2(dba)3 and the ligand DPEphos effects intramolecular C-O bond formation between enolates and aryl halides in the conversion of 1-(2-haloaryl)ketones directly into the corresponding benzofurans. Both cyclic and acyclic ketones are efficient substrates. Thio ketones can also be employed allowing the preparation of the corresponding benzothiophenes.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Dec
pubmed:issn	1523-7060
pubmed:author	pubmed-author:GillmoreAdam TAT, pubmed-author:TaylorDawnD, pubmed-author:WillisMichael CMC
pubmed:issnType	Print
pubmed:day	9
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4755-7
pubmed:year	2004
pubmed:articleTitle	Palladium-catalyzed intramolecular O-arylation of enolates: application to benzo[b]furan synthesis.
pubmed:affiliation	Department of Chemistry, University of Bath, Bath BA2 7AY, UK. m.c.willis@bath.ac.uk
pubmed:publicationType	Journal Article