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Cinnamaldehyde citronellol

Recently, it has been shown that ultrasonic agitation during hydrogenation reactions over skeletal nickel can slow catalyst deactivation [122-124], Furthermore, ultrasonic waves can also significantly increase the reaction rate and selectivity of these reactions [123,124], Cavitations form in the liquid reaction medium because of the ultrasonic agitation, and subsequently collapse with intense localized temperature and pressure. It is these extreme conditions that affect the chemical reactions. Various reactions have been tested over skeletal catalysts, including xylose to xylitol, citral to citronellal and citronellol, cinnamaldehyde to benzenepropanol, and the enantioselective hydrogenation of 1-phenyl-1,2-propanedione. Ultrasound supported catalysis has been known for some time and is not peculiar to skeletal catalysts [125] however, research with skeletal catalysts is relatively recent and an active area. [Pg.151]

Citral Citronellol Coumarin Eugenol Farnesol Geraniol Hexyl cinnamaldehyde [Hexyl cinnamal]... [Pg.191]

See other pages where Cinnamaldehyde citronellol is mentioned: [Pg.3541]    [Pg.3541]    [Pg.727]    [Pg.257]    [Pg.687]    [Pg.457]    [Pg.459]    [Pg.1221]    [Pg.880]    [Pg.73]    [Pg.1317]    [Pg.186]   
See also in sourсe #XX -- [ Pg.11 ]



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Cinnamaldehyde

Citronellol

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