The first total synthesis of iPF4α-VI and its deuterated analog
✍ Scribed by Seongjin Kim; John A. Lawson; Domenico Praticò; Garret A. FitzGerald; Joshua Rokach
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 119 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The total and stereospecific syntheses of iPF 4a -VI and d 4 -iPF 4a -VI have been accomplished. iPF 4a -VI is a docosahexanenoic acid (DHA)-derived isoprostane. DHA is the most abundant polyunsaturated fatty acid in the brain. Different synthetic designs have been used for the two syntheses. In the d 4 -iPF 4a -VI design, the deuterated part of the molecule was introduced last in the synthesis.
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