Issue 1, 1997

Synthesis of Saturated Anacardic Acids, and Alkenyl and Alkynyl Analogues†

Abstract

The C-alkylation of esters of 2-methoxy-6-methylbenzoic acid and of the 4-methyl isomers affords a route to homologous compounds of the natural anacardic acid series and of the unnatural isoanacardic acids respectively; ω-alkenyl and ω-alkynyl compounds suitable for synthesising other natural phenolic lipids or for structure–activity studies are also accessible.

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 14-15

Synthesis of Saturated Anacardic Acids, and Alkenyl and Alkynyl Analogues†

J. H. P. Tyman and N. Visani, J. Chem. Res. (S), 1997, 14 DOI: 10.1039/A605538I

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements