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Creators/Authors contains: "Clarkson, Aidan"

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  1. ; ; ; (, American Chemical Society)
    An acid-promoted dearomative rearrangement of O-arylhydroxylamines affords 2-aminocyclohexadien-1-ones, which can in turn be reductively quenched for the synthesis of trans-aminoalcohols on a cyclohexadiene core. This method serves as an efficient entry to the pharmaceutically relevant 1-arylcyclohexylamine scaffold in two steps (one purification) from commercially available or readily prepared 2-arylphenols. 
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  2. ; ; ; (, Organic Letters)
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