Practical, Stereoselective Synthesis of Cecropia Juvenile Hormone
AUTOR(ES)
Tamelen, E. E. Van
RESUMO
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.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=389175Documentos Relacionados
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- Synthesis of a material with high juvenile hormone activity.
