BIOCHEMICAL PREPARATIONS OF BOTH THE ENANTIOMERS OF METHYL 3-HYDROXYPENTANOATE AND THEIR CONVERSION TO THE ENANTIOMERS OF 4-HEXANOLIDE, THE PHEROMONE OF TROGODERMA GLABRUM

DOI: 10.1016/S0040-4020(01)96410-5

Source and publish data:

Tetrahedron p. 919 - 926 (1985)

Update date:2022-07-31

Topics:

Authors:

Mori, Kenji

Mori, Hideto

Sugai, Takeshi

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Article abstract of DOI:10.1016/S0040-4020(01)96410-5

Both the enantiomers of methyl 3-hydroxypentanoate were prepared by microbial asymmetric reduction of 3-oxopentanoic esters.Conversion of methyl 3-hydroxypentanoate to 4-hexanolide, the pheromone of Trogoderma glabrum, was achieved.

Full text of DOI:10.1016/S0040-4020(01)96410-5

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