Source:http://linkedlifedata.com/resource/pubmed/id/16496976
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-2-24
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pubmed:abstractText |
The reactions of vinylidencyclopropanes 1 with diphenyl diselenide 2 in the presence of AIBN produced the corresponding products 4 or 5 in moderate to good yields under mild conditions. The transformation of 4 to the corresponding methylenecyclopropanes 6 was achieved by treatment with hydrogen peroxide (H2O2) in toluene, and these were further transformed to the corresponding naphthalene derivatives 7 by treatment with 30 mol % of TfOH in dichloromethane.
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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 |
0022-3263
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
71
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1920-3
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pubmed:year |
2006
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pubmed:articleTitle |
Reactions of vinylidenecyclopropanes with diphenyl diselenide in the presence of AIBN and further transformation to produce new naphthalene derivatives.
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pubmed:affiliation |
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China. mshi@pub.sioc.ac.cn
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pubmed:publicationType |
Journal Article
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