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Jocelyn G. Millar

Researcher at University of California, Riverside

Publications -  454
Citations -  13748

Jocelyn G. Millar is an academic researcher from University of California, Riverside. The author has contributed to research in topics: Sex pheromone & Pheromone. The author has an hindex of 57, co-authored 435 publications receiving 12421 citations. Previous affiliations of Jocelyn G. Millar include National Research Council & University of California, Berkeley.

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Stereoselective synthesis of the obscure mealybug pheromone by hydrogenation of a tetrasubstituted alkene precursor

TL;DR: An improved diastereoselective synthesis of (1R∗,2R ∗,3S∗)-1-acetoxymethyl-2,3,4, 4, 4-tetramethylcyclopentane, the sex pheromone of the obscure mealybug, Pseudococcus viburni, is described in this article.
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Conserved male-specific cuticular hydrocarbon patterns in the trap-jaw ant Odontomachus brunneus

TL;DR: Male-specific cuticular hydrocarbon patterns for the trap-jaw ant Odontomachus brunneus are reported, demonstrating that male-specific overabundance of four hydrocarbons is conserved across populations despite population-level divergence of the remainder of the profile.
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Syntheses and determination of absolute configurations and biological activities of the enantiomers of the longtailed mealybug pheromone.

TL;DR: Comparison of the biological activities of both enantiomers and the racemate in field trials showed that the (S)-(+)-enantiomer was highly attractive to male mealybugs, strongly suggesting that female longtailed mealybug produce this enantiomer.
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Development of a High-Throughput Laboratory Bioassay for Testing Potential Attractants for Terrestrial Snails and Slugs.

TL;DR: Ch chopped cucumber was as attractive or more attractive than any other substrate tested, and chopped fresh cucumber (Cucumis sativus) was the most attractive substrate for both species.
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Sex Attractant Pheromone of Saturniid Moth Coloradia velda

TL;DR: The female-produced sex attractant pheromone of Coloradia velda has been identified by a combination of analytical methods and field tests as a blend of ( 10E,12Z)-hexadecadien-1-yl acetate, (10E, 12Z–16:Ac), (10 E,12E)- hexadec adenine acetate and (10e, 12E–16):Ac in a 10:1:0.33 ratio.