Source:http://linkedlifedata.com/resource/pubmed/id/16591739
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-6-29
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pubmed:abstractText |
Methyl cis-10-epoxy-3,7,11-trimethyl-trans,trans-2,6-tridecadienoate has been stereoselectively synthesized in 12 steps starting from methyl trans-gamma-bromo-beta,beta-dimethylacrylate and 1-acetyl-1-methylcyclopropane. The final product proved to be identical with the second, less abundant juvenile hormone (methyl 12-homojuvenate) isolated from the Cecropia silk moth. The biological activities of the compound were evaluated in various insects.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16591739-16591663,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16591739-5836318,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16591739-5848789,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16591739-5848792
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0027-8424
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1005-9
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pubmed:dateRevised |
2010-9-14
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pubmed:year |
1969
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pubmed:articleTitle |
Total synthesis of the racemic form of the second juvenile hormone (methyl 12-homojuvenate) from the cecropia silk moth.
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pubmed:affiliation |
DEPARTMENT OF CHEMISTRY, STANFORD UNIVERSITY.
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pubmed:publicationType |
Journal Article
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