ChemInform Abstract: Synthetic Approaches to 2-(4-Hydroxy-7-chromanyl)benzoic Acids as Antagonists of Leukotriene B4.
โ Scribed by R. J. CHAMBERS; K. KOCH; M. S. BIGGERS; M. RAMCHANDANI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 43 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Synthetic Approaches to 2-(4-Hydroxy-7-chromanyl)benzoic Acids as Antagonists of Leukotriene B 4 .
-Two different ways to prepare desired title compounds (VII) and (XI) are used. The first includes seven steps, uses organostannane biaryl coupling and non-stereoselective reduction, which limits this reaction type in his further application. The second route is found to be efficient, is complete within four steps and involves a palladium-catalyzed coupling of ortho-metalated aryl oxazolines in tandem with stereospecific enone reduction as key steps. -(CHAMBERS, R.
๐ SIMILAR VOLUMES
A Short and Efficient Synthesis of 4-[2,2-Dimethyl-4(tol-4yl)benzochrom-3-en-7-yl]benzoic Acid. A Potent Retinoic Acid Receptor Antagonist. -A procedure for the synthesis of title compound (X) is given. The procedure is amenable to large-scale preparation. -