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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1977 Feb;74(2):419–422. doi: 10.1073/pnas.74.2.419

Characterization and synthesis of volatile compounds from the defensive secretions of some "daddy longlets" (Arachnida: Opiliones: Leiobunum spp.).

T H Jones, J Meinwald, K Hicks, T Eisner
PMCID: PMC392299  PMID: 265514

Abstract

Analyses of the chief volatile constituents of the defensive secretions of three oplionids were carried out. Leiobunum nigripalpi produces three closely related C7 compounds: E-4-methyl-4-hexen-3-one(I), 4-methylhexan-3-one(II), and 4-methylhexan-3-ol(III), along with E-4-methyl-4-hepten-3-one(IV), E,E-2,4-dimethylhexa-2,4-dienal(IX), and a minor, unidentified component. L. leiopenis secretion contains E-4-methyl-4-hepten-3-one(IV), 4-methylheptan-3-one(V), E,E-2,4-dimethylhexa-2,4-dien-1-ol(VII), and E,E-2,4-dimethylhepta-2,4-dien-1-ol(VIII). L. calcar yields chiefly E-4,6-dimethyl-6-octen-3-one(VI) and E,E-2,4-dimethylhexa-2,4-dien-1-ol(VII). Six of these compounds are new natural products. The structures of these compounds, which can be regarded either as polyketide-derived or as modified isoprenoids, raise interesting biosynthetic questions.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Meinwald J., Kluge A. F., Carrel J. E., Eisner T. Acyclic ketones in the defensive secretion of a "daddy longlegs" (Leiobunum vittatum). Proc Natl Acad Sci U S A. 1971 Jul;68(7):1467–1468. doi: 10.1073/pnas.68.7.1467. [DOI] [PMC free article] [PubMed] [Google Scholar]
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