4.8 Article

Multiple regioselective functionalizations of quinolines via magnesiations

Journal

ORGANIC LETTERS
Volume 9, Issue 26, Pages 5525-5528

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol702494k

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A wide range of polyfunctionalized quinolines was prepared via chemo- and regioselective magnesiation reactions using appropriate Mg reagents, such as i-PrMgCl center dot LiCl, MesMgBr center dot LiCl, Mes(2)Mg center dot 2LiBr, TMPMgCl-LiCl, and TMP2Mg center dot 2LiCl. An application to the total synthesis of the biologically active compound talnetant was performed (six steps, 28%).

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