SYNTHESIS AND BIOLOGICAL ACTIVITY OF OPTICALLY ACTIVE FORMS OF (E)-3,7-DIMETHYL-2-OCTENE-1,8-DIOLIC ACID (CALLOSOBRUCHUSIC ACID); A COMPONENT OF THE COPULATION RELEASE PHEROMONE (ERECTIN) OF THE AZUKI BEAN WEEVIL

DOI: 10.1016/S0040-4020(01)91957-X

Source and publish data:

Tetrahedron p. 2303 - 2306 (1983)

Update date:2022-08-05

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Authors:

Mori, Kenji

Ito, Teruhito

Tanaka, Kaoru

Honda, Hiroshi

Yamamoto, Izuru

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Article abstract of DOI:10.1016/S0040-4020(01)91957-X

Both enantiomers of callosobruchusic acid were synthesized, confirming its proposed plane structure as (E)-3,7-dimethyl-2-octene-1,8-dioic acid.Both of them were biologically active as the copulation release pheromone of Callosobruchus chinensis L.

Full text of DOI:10.1016/S0040-4020(01)91957-X

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