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16288550
Source:
http://linkedlifedata.com/resource/pubmed/id/16288550
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pubmed-article:16288550
rdf:type
pubmed:Citation
lld:pubmed
pubmed-article:16288550
lifeskim:mentions
umls-concept:C0034255
lld:lifeskim
pubmed-article:16288550
lifeskim:mentions
umls-concept:C1522240
lld:lifeskim
pubmed-article:16288550
pubmed:issue
24
lld:pubmed
pubmed-article:16288550
pubmed:dateCreated
2005-11-18
lld:pubmed
pubmed-article:16288550
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.
lld:pubmed
pubmed-article:16288550
pubmed:language
eng
lld:pubmed
pubmed-article:16288550
pubmed:journal
http://linkedlifedata.com/r...
lld:pubmed
pubmed-article:16288550
pubmed:status
PubMed-not-MEDLINE
lld:pubmed
pubmed-article:16288550
pubmed:month
Nov
lld:pubmed
pubmed-article:16288550
pubmed:issn
1523-7060
lld:pubmed
pubmed-article:16288550
pubmed:author
pubmed-author:CoreyE JEJ
lld:pubmed
pubmed-article:16288550
pubmed:author
pubmed-author:TianYuanY
lld:pubmed
pubmed-article:16288550
pubmed:issnType
Print
lld:pubmed
pubmed-article:16288550
pubmed:day
24
lld:pubmed
pubmed-article:16288550
pubmed:volume
7
lld:pubmed
pubmed-article:16288550
pubmed:owner
NLM
lld:pubmed
pubmed-article:16288550
pubmed:authorsComplete
Y
lld:pubmed
pubmed-article:16288550
pubmed:pagination
5535-7
lld:pubmed
pubmed-article:16288550
pubmed:year
2005
lld:pubmed
pubmed-article:16288550
pubmed:articleTitle
Selective 4-arylation of pyridines by a nonmetalloorganic process.
lld:pubmed
pubmed-article:16288550
pubmed:affiliation
Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA. corey@chemistry.harvard.edu
lld:pubmed
pubmed-article:16288550
pubmed:publicationType
Journal Article
lld:pubmed
http://linkedlifedata.com/r...
pubmed:referesTo
pubmed-article:16288550
lld:pubmed