16288550

Source:http://linkedlifedata.com/resource/pubmed/id/16288550

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0034255, umls-concept:C1522240
pubmed:issue	24
pubmed:dateCreated	2005-11-18
pubmed:abstractText	[reaction: see text] Mild and position-selective nucleophilic 4-arylation of pyridines has been accomplished by the use of triflic anhydride N-activation.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Nov
pubmed:issn	1523-7060
pubmed:author	pubmed-author:CoreyE JEJ, pubmed-author:TianYuanY
pubmed:issnType	Print
pubmed:day	24
pubmed:volume	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5535-7
pubmed:year	2005
pubmed:articleTitle	Selective 4-arylation of pyridines by a nonmetalloorganic process.
pubmed:affiliation	Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA. corey@chemistry.harvard.edu
pubmed:publicationType	Journal Article