The alkenyl acetates £9-12:Ac, zl l l -12:Ac and Zl l -14:Ac were identified as minor components of the C. murinana female pheromone blend by chemical analyses of volatile pheromone gland constituents and potential pheromone precursors, electrophysiological recordings from single receptor cells, and field trapping tests. Gland washes from virgin females contained these compounds at 3%, 10% and ...

In moths, the components of the female pheromone blend are detected in the male antennae by pheromone olfactory receptor neurons (Ph-ORNs) expressing narrowly tuned olfactory receptors. Responses to sex pheromones have generally been thought to be independent from the odorant background. However, interactions between pheromone components and plant volatiles have been reported at behavioral and ...

The first general method for the reductive dimerization of alkyl halides, alkyl mesylates, alkyl trifluoroacetates, and allylic acetates is reported which proceeds with low catalyst loading (0.5 to 5 mol%), generally high yields (80% ave yield), and good functional-group tolerance.

This paper describes the application of a new methodology to structural analysis of complex carbohydrates, in this case a bacterial antigenic polysaccharide, utilizing gas chromatography for the separation and tentative identification and mass spectroscopy for positive identification of partially methylated alditol acetates obtained from the original and partially degraded polysaccharide. [The ...

[reaction: see text] The Rh-TangPhos catalyst has been used for asymmetric hydrogenation of itaconic acid and enol acetate derivatives. A variety of chiral 2-substituted succinic acids and chiral acetates have been obtained in excellent ee values (up to 99% ee).

The arylation of bicyclic oxathiane glycosyl donors has been achieved using benzyne generated in situ from 1-aminobenzotriazole (1-ABT) and lead tetraacetate. Following sulfur arylation, glycosylation of acetate ions proceeded with high levels of stereoselectivity to afford α -glycosyl acetates in a 'one-pot' reaction, even in the presence of alternative acceptor alcohols.

Novel 2,3-dihydro-4-pyridinones were synthesized via the reaction of curcumin and primary amines or amine acetates under microwave irradiation. Montmorillonite K-10 was used as a catalyst. Reaction times did not exceed 120 s. The structures of the compounds were established by elemental analysis and from their mass, 1H- and 13C-NMR spectra.