Pheromone synthesis—63 Synthesis of both the enantiomers of 2,3-dihydro-2- isopropyl-2,5-dimethylfuran, a sex specific compound in females of the beetle hylecoetus dermestoidesL☆

Add time:08/12/2019    Source:sciencedirect.com

Both the enantiomers of 2,3-dihydro-2-isopropyl-2,5-dimethylfuran were synthesized employing the Sharpless asymmetric epoxidation reaction. The (R)-(—)-enantiomer of this cyclic enol ether was also synthesized starting from (R)-(—)-linalool.

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