4.8 Article

A general [3+2+1] annulation strategy for the preparation of pyridine N-oxides

Journal

ORGANIC LETTERS
Volume 3, Issue 2, Pages 209-211

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol006831r

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[GRAPHICS] Stabilized ketone, aldehyde, and ester enolates react with vinamidinium hexafluorophosphate salts and hydroxylamine hydrochloride to give access to the corresponding pyridine N-oxides, The annulation reactions proceed in good to excellent yields with vinamidinium salts with a range of beta -substituents (R-3 = halo, aryl, nitro, trifluoromethyl).

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