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- W2328133772 abstract "A series of dihydroxyacetone monoesters, characterized by branching, cyclization, and unsaturation in the carboxylic acid component, was synthesized, and the repellency of the novel compounds against Aedes aegypti (L.) mosquitoes was determined. In evaluations, compounds with a single branch in the chain were among the more active derivatives; i.e., dihydroxyacetone mono (4-methylpentanoate) (III) and dihydroxyacetone mono (2-methyl-hexanoate) (VII) have an efficacy paralleling that of dihydroxyacetone monohexanoate (I), particularly under conditions in which perspiration was induced in human volunteers. Compounds with more extensive branching, cyclization, or unsaturation, were less efficacious. Compound I had an activity comparable to that of a N, N. diethyl-m-toluamide (deet) standard, although at a greater concentration." @default.
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- W2328133772 date "1972-02-01" @default.
- W2328133772 modified "2023-10-14" @default.
- W2328133772 title "Dihydroxyacetone Monoester Mosquito Repellents. Effect of Branching, Cyclization, and Unsaturation upon Repellent Efficacy1" @default.
- W2328133772 doi "https://doi.org/10.1093/jee/65.1.66" @default.
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