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pubmed-article:16591739pubmed:dateCreated2010-6-29lld:pubmed
pubmed-article:16591739pubmed:abstractTextMethyl 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.lld:pubmed
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pubmed-article:16591739pubmed:statusPubMed-not-MEDLINElld:pubmed
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pubmed-article:16591739pubmed:issn0027-8424lld:pubmed
pubmed-article:16591739pubmed:authorpubmed-author:JohnsonW SWSlld:pubmed
pubmed-article:16591739pubmed:authorpubmed-author:Krishnakumara...lld:pubmed
pubmed-article:16591739pubmed:authorpubmed-author:CampbellS FSFlld:pubmed
pubmed-article:16591739pubmed:authorpubmed-author:MeyerA SASlld:pubmed
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pubmed-article:16591739pubmed:volume62lld:pubmed
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pubmed-article:16591739pubmed:pagination1005-9lld:pubmed
pubmed-article:16591739pubmed:dateRevised2010-9-14lld:pubmed
pubmed-article:16591739pubmed:year1969lld:pubmed
pubmed-article:16591739pubmed:articleTitleTotal synthesis of the racemic form of the second juvenile hormone (methyl 12-homojuvenate) from the cecropia silk moth.lld:pubmed
pubmed-article:16591739pubmed:affiliationDEPARTMENT OF CHEMISTRY, STANFORD UNIVERSITY.lld:pubmed
pubmed-article:16591739pubmed:publicationTypeJournal Articlelld:pubmed
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