Dianions of unsaturated carboxylic acids in synthesis. Synthesis of juvocimene I

Article abstract of DOI:10.1080/00397919608003490

Juvocimene I is prepared by a non ambiguous synthesis based on the regioselective alkylation of 4-methylhexa-2,4-dienoic acid, and Wittig olefination of the aldehyde corresponding to the alkylated acid.

Full text of DOI:10.1080/00397919608003490

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Dianions of Unsaturated
Carboxylic Acids in Synthesis.
Synthesis of Juvocimene I
R. Mestres a & E. Muñoz a
a Department de Química Orgànica , Universitat de
València , Dr. Moliner 50, 46100, Burjassot, València,
Spain
Published online: 15 Aug 2006.
To cite this article: R. Mestres & E. Muñoz (1996) Dianions of Unsaturated Carboxylic
Acids in Synthesis. Synthesis of Juvocimene I, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:7,
1309-1319, DOI: 10.1080/00397919608003490
To link to this article: http://dx.doi.org/10.1080/00397919608003490
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