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Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
Synthesis of Spirocyclic Piperidines by Radical Hydroarylation
Racheal M Spurlin1, Amber L Harris1, Cameron J Pratt1
1Department of Chemistry, Emory University, Atlanta, GA 30322, USA.
Abstract:
Reported here are conditions for the construction of spirocyclic piperidines from linear aryl halide precursors. These conditions employ a strongly reducing organic photoredox catalyst in combination with a trialkylamine reductant to achieve formation of aryl radical species. Regioselective cyclization followed by hydrogen-atom transfer affords a range of complex spiropiperidines. This system operates efficiently under mild conditions without the need for toxic reagents or precious metals.
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