THE STEREOSPECIFIC PREPARATION OF METHYL FARNESOATE AND SYNTHETIC PRECURSORS OF C18- AND C17 JUVENILE HORMONES
- 5 December 1974
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 3 (12) , 1425-1428
- https://doi.org/10.1246/cl.1974.1425
Abstract
The new method for the stereospecific preparation of 1,5-diene units was successfully applied to the syntheses of methyl farnesoate and the synthetic precursors of C18- and C17 juvenile hormones, 15 and 20.Keywords
This publication has 3 references indexed in Scilit:
- THE HIGHLY STEREOSELECTIVE SYNTHESIS OF ETHYL GERANATEChemistry Letters, 1974
- THE STEREOSPECIFIC PREPARATION OF TRISUBSTITUTED OLEFINSChemistry Letters, 1973
- A highly stereoselective synthesis of (2Z,6E)-7-methyl-3-propyl-2,6-decadien-1-ol. A proposed revision in the stereochemistry of a tetrahomoterpene isolated from the colding mothTetrahedron Letters, 1973