Synthesis of (5E,9E)-5,9-Hexacosadienoic Acid via Copper- and Palladium-Mediated Reactions Using 1-Acetoxy-4-chloro-2-butene as a Synthon.
- 1 January 1988
- journal article
- research article
- Published by Danish Chemical Society in Acta Chemica Scandinavica
- Vol. 42b (6) , 397-402
- https://doi.org/10.3891/acta.chem.scand.42b-0397
Abstract
A synthesis of (5E,9E)-5,9-hexacosadienoic acid (1), a double-bond isomer of a marine natural product, was performed using 1-acetoxy-4-chloro-2-butene (2) as a building block.This publication has 3 references indexed in Scilit:
- Phospholipid studies of marine organisms. 7. Stereospecific synthesis of (5Z,9Z)-, (5Z,9E)-, (5E,9Z)-, and (5E,9E)-5,9-hexacosadienoic acidThe Journal of Organic Chemistry, 1984
- Synthesis of the major pheromonal component of the Monarch butterfly (Danaus plexippus) via palladium-catalyzed 1,4-functionalization of isopreneThe Journal of Organic Chemistry, 1983
- Organopalladium Compounds in Organic Synthesis and in CatalysisPublished by Elsevier ,1982