Source:http://linkedlifedata.com/resource/pubmed/id/19718728
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
38
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| pubmed:dateCreated |
2009-9-28
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| pubmed:abstractText |
Recent breakthroughs have proved that direct palladium(II)-catalyzed allylic C-H alkylation can be achieved. This new procedure shows that the inherent requirement for a leaving group in the Tsuji-Trost palladium-catalyzed allylic alkylation can be lifted. These initial reports hold great promise for the development of allylic C-H alkylation into a widely applicable methodology, thus providing a means to enhance synthetic efficiency in these reactions.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:month |
Sep
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| pubmed:issn |
1521-3765
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:day |
28
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| pubmed:volume |
15
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
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| pubmed:pagination |
9632-6
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| pubmed:year |
2009
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| pubmed:articleTitle |
Toward efficient palladium-catalyzed allylic C-H alkylation.
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| pubmed:affiliation |
Department of Chemistry, Technical University of Denmark, Kemitorvet, building 207, Denmark.
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| pubmed:publicationType |
Journal Article
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