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 DERMESTOIDES L

DOI: 10.1016/S0040-4020(01)91128-7

Source and publish data:

Tetrahedron p. 1761 - 1766 (1984)

Update date:2022-08-04

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Authors:

Mori, Kenji

Ebata, Takashi

Takechi, Shozo

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Article abstract of DOI:10.1016/S0040-4020(01)91128-7

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 from (R)-(-)-linalool.

Full text of DOI:10.1016/S0040-4020(01)91128-7

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