Source:http://linkedlifedata.com/resource/pubmed/id/14995184
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2004-3-3
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pubmed:abstractText |
The rhodium-catalyzed carbonylative [3+2+1] cycloaddition of trienes into bicyclohexenones has been developed. The carbonylated cycloaddition products have a high regioselectivity. This catalytic system tolerates functionalities including ether, sulfonamide, and ester.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0002-7863
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
126
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2714-5
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pubmed:dateRevised |
2008-1-17
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pubmed:year |
2004
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pubmed:articleTitle |
Rhodium-catalyzed carbonylative [2+2+1] cycloaddition reactions: catalytic formation of bicyclic cyclohexenones [corrected].
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pubmed:affiliation |
School of Chemistry and Center for Molecular Catalysis, Seoul National University, Seoul 151-747, Korea.
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pubmed:publicationType |
Journal Article,
Comment
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