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Proc Natl Acad Sci U S A ; 68(6): 1294-5, 1971 Jun.
Article in English | MEDLINE | ID: mdl-5288378

ABSTRACT

The high-yield, stereoselective conversion of geraniol (3,7-dimethyl-trans-2,6-octadien-1-ol) to the insect juvenile hormone, methyl 12,14-dihomojuvenate (methyl cis-10-epoxy-3,11-dimethyl-7-ethyl-trans, trans-2,6-tridecadienoate), has been performed by means of a nine-step route that avoids chromatography of intermediates.


Subject(s)
Juvenile Hormones/chemical synthesis , Methods , Stereoisomerism
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