Abstract
Pd-catalyzed coupling of aryl halides with TeocNHOTBS, followed by treatment of the products with TBAF, provides effective access to a wide range of N-arylhydroxylamines by a route that produces stable doubly-protected intermediates and allows the protective groups to be removed under mild conditions that do not cause extensive degradation of the final product.
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CITATION STYLE
APA
Beaudoin, D., & Wuest, J. D. (2011). Synthesis of N-arylhydroxylamines by Pd-catalyzed coupling. Tetrahedron Letters, 52(17), 2221–2223. https://doi.org/10.1016/j.tetlet.2010.12.034
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