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Synthesis of p-Santalol

The synthesis starts from norbornanone (6.37). This is methylated using iodomethane with sodamide as the base. Alkylation of methyl-norbornanone (6.38), norbornanone (6.37) with Buchi s bromide (6.39) (prepared by addition of hydrogen bromide to acrolein in ethylene [Pg.146]


As an example of the synthesis of p-santalol, we will look at that of Erman and Kretschmar, since it also illustrates two interesting points of general relevance. The overall scheme is shown in Figure 6.8. [Pg.145]

Scheme 15.12 Synthesis of the pheromone 2.6-dimethyl-1.5-heptadiene-3-n1 acetate. Scheme 15.13 Synthesis of p-santalol. Scheme 15.12 Synthesis of the pheromone 2.6-dimethyl-1.5-heptadiene-3-n1 acetate. Scheme 15.13 Synthesis of p-santalol.

See other pages where Synthesis of p-Santalol is mentioned: [Pg.145]    [Pg.563]   
See also in sourсe #XX -- [ Pg.8 , Pg.145 , Pg.146 ]




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