Enantioselective Synthesis of Juvenile Hormone III in Three Steps from Methyl Farnesoate
- 1 January 1993
- journal article
- research article
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 1993 (08) , 777-779
- https://doi.org/10.1055/s-1993-25939
Abstract
The asymmetric dihydroxylation of methyl farnesoate resulted in regioselective dihydroxylation of the 10, 11 olefin to give the (10S)and (10R) -(2E,6E)-10,11-dihydroxy-3,7,11-trimethyI-2,6-dodecadienoates in high ee. These diols were converted to juvenile hormone III and its enantiomer.Keywords
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