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ChemInform Abstract: Synthetic Approaches to 2-(4-Hydroxy-7-chromanyl)benzoic Acids as Antagonists of Leukotriene B4.

โœ 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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โœฆ 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.


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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. -