Source:http://linkedlifedata.com/resource/pubmed/id/11772102
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
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| pubmed:dateCreated |
2002-1-4
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| pubmed:abstractText |
[reaction: see text] The palladium-catalyzed coupling reaction of potassium alkenyltrifluoroborates with aryl or alkenyl halides or triflates proceeds readily with good yields. The trifluoroborates are air- and moisture-stable solids that can be stored indefinitely. The cross-coupling can be effected using PdCl(2)(dppf).CH(2)Cl(2) as the catalyst in n-PrOH in the presence of Et(3)N. A variety of functional groups are tolerated.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:month |
Jan
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| pubmed:issn |
1523-7060
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:day |
10
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| pubmed:volume |
4
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
107-9
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| pubmed:dateRevised |
2003-10-31
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| pubmed:year |
2002
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| pubmed:articleTitle |
Suzuki cross-coupling reactions of potassium alkenyltrifluoroborates.
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| pubmed:affiliation |
Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, USA. gmolandr@sas.upenn.edu
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| pubmed:publicationType |
Journal Article
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