N-o cleavage reactions of heterobicycloalkene-fused 2-isoxazolines

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Abstract

Transition metal-mediated N-O bond cleavage reactions of heterobicycloalkene-fused 3-methyl-2-isoxazolines were investigated. Optimal cleavage conditions were found with Raney nickel/ AlCl3 mediation in aqueous methanol. The reaction provided a diverse collection of novel heterobicycle-fused β-hydroxyketones with good to excellent yields (66-95%) and without the need for chromatographic purification.

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Nagireddy, J. R., Tranmer, G. K., Carlson, E., & Tam, W. (2014). N-o cleavage reactions of heterobicycloalkene-fused 2-isoxazolines. Beilstein Journal of Organic Chemistry, 10, 2200–2205. https://doi.org/10.3762/bjoc.10.227

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