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A-Pinene rearrangement

Epoxy-a-pinene, produced by epoxidation of (+)-a-pinene, rearranges in the presence of Lewis acids to (-)-campholenealdehyde which is not only one of the constituents of various juniper species, but also the starting reagent for the synthesis of fragrances with the odor of sandalwood. Sandalore, for example, is produced by Knoevenagel aUcenylation of campholenealdehyde with propanal followed by reduction of the aldehyde function with sodium borohydride... [Pg.126]

See other pages where A-Pinene rearrangement is mentioned: [Pg.54]

See also in sourсe #XX -- [ Pg.3 , Pg.705 , Pg.771 ]

See also in sourсe #XX -- [ Pg.705 , Pg.771 ]

See also in sourсe #XX -- [ Pg.3 , Pg.705 , Pg.771 ]

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2 -Pinen

2-Pinene

A rearrangements

A-Pinenes

Pinenes, rearrangement