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Marmelo oxides A and

The reaction was applied to an acyclic system for the synthesis of furanoid terpenes (Scheme ll)51. The palladium-catalyzed intramolecular reaction of 47 afforded 48 which was transformed to the target molecule. The latter product was obtained as a 1 1 mixture of marmelo oxide A and B, which is the isomeric mixture found in nature. [Pg.669]

Synthetic Applications In several syntheses toward naturally occurring furanoid terpenes, the intramolecular oxyacetoxylation was applied as a key step [125]. For example, in the synthesis of marmelo oxides A and B,... [Pg.912]


See other pages where Marmelo oxides A and is mentioned: [Pg.199]    [Pg.266]    [Pg.469]    [Pg.374]    [Pg.375]    [Pg.912]    [Pg.418]    [Pg.647]    [Pg.199]    [Pg.266]    [Pg.469]    [Pg.374]    [Pg.375]    [Pg.912]    [Pg.418]    [Pg.647]    [Pg.912]    [Pg.311]    [Pg.418]    [Pg.224]    [Pg.304]    [Pg.425]    [Pg.224]   
See also in sourсe #XX -- [ Pg.374 , Pg.375 ]




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Marmelo oxides

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