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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
18
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pubmed:dateCreated |
2008-9-16
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pubmed:abstractText |
Mild conditions have been developed to achieve Pd(OAc)2-catalyzed regioselective cross-coupling between indoles and potassium aryltrifluoroarylborates in the presence of Cu(OAc)2 in acetic acid at room temperature. A variety of potassium aryltrifluoroborates selectively undergo the direct arylation across indoles and afford 2-aryl indoles in moderate to good yields.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1520-6904
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
19
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7428-31
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pubmed:meshHeading |
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pubmed:year |
2008
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pubmed:articleTitle |
Palladium-catalyzed direct C-2 arylation of indoles with potassium aryltrifluoroborate salts.
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pubmed:affiliation |
Department of Chemistry, Zhejiang University, Hangzhou 310027, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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