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Characterization of posticlure and the structure-related sex pheromone candidates prepared by epoxidation of (6 Z,9 Z,11 E)-6,9,11-trienes and (3 Z,6 Z,9 Z,11 E)-3,6,9,11-tetraenes.
- Source :
-
Analytical & Bioanalytical Chemistry . Sep2013, Vol. 405 Issue 23, p7405-7414. 10p. - Publication Year :
- 2013
-
Abstract
- trans-11,12-Epoxy-(6 Z,9 Z)-6,9-henicosadiene (posticlure) has been identified from a pheromone gland of the lymantriid species, Orgyia postica. Since the diversity of Lepidoptera suggests that some species utilize the structure-related epoxy compound as a sex pheromone component, epoxydienes and epoxytrienes derived from (6 Z,9 Z,11 E)-6,9,11-trienes and (3 Z,6 Z,9 Z,11 E)-3,6,9,11-tetraenes with a C-C chain were systematically synthesized and the chemical data were accumulated in order to contribute to a new pheromone research. Peracid oxidation of each triene and each tetraene produced, respectively, a mixture of three epoxydienes ( cis-6,7-epoxy-9,11-diene; cis-9,10-epoxy-6,11-diene; and trans-11,12-epoxy-6,9-diene) and four epoxytrienes ( cis-3,4-epoxy-6,9,11-triene; cis-6,7-epoxy-3,9,11-triene; cis-9,10-epoxy-3,6,11-triene; and trans-11,12-epoxy-3,6,9-triene). While the 9,10-epoxy compounds were unstable and, interestingly, converted into 9-ketone derivatives after chromatography over SiO, each positional isomer was isolated by HPLC equipped with an ODS column, and the chemical structure was determined by NMR analysis. On the GC-MS analysis with a DB-23 column, the positional isomers were also eluted separately and characteristic mass spectra were proposed. By comparing the spectral data of the epoxy compounds with a different carbon chain, diagnostic fragment ions reflecting the chemical structure were determined as follows: m/z 79, 109, 113, and M-114 for the 6,7-epoxydienes; m/z 69, 97, 111, 139, and M-111 for the 9,10-epoxydienes; m/z 57, 79, 109, 136, M-151, and M-111 for the 11,12-epoxydienes; m/z 79, 91, 105, and 119 for the 3,4-epoxytrienes; m/z 79, 124, M-124, M-96, and M-69 for the 6,7-epoxytrienes; m/z 79, 95, 109, 137, and M-108 for the 9,10-epoxytrienes; and m/z 79, 134, M-149, M-109, and M-95 for the 11,12-epoxytrienes. [ABSTRACT FROM AUTHOR]
- Subjects :
- *PHEROMONES
*EPOXIDATION
*TRIENES
*TETRAENES
*LYMANTRIIDAE
*ORGYIA
Subjects
Details
- Language :
- English
- ISSN :
- 16182642
- Volume :
- 405
- Issue :
- 23
- Database :
- Academic Search Index
- Journal :
- Analytical & Bioanalytical Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 90016021
- Full Text :
- https://doi.org/10.1007/s00216-013-7144-2