Beilstein Journal of Organic Chemistry (Jul 2024)

Oxidation of benzylic alcohols to carbonyls using N-heterocyclic stabilized λ3-iodanes

  • Thomas J. Kuczmera,
  • Pim Puylaert,
  • Boris J. Nachtsheim

DOI
https://doi.org/10.3762/bjoc.20.149
Journal volume & issue
Vol. 20, no. 1
pp. 1677 – 1683

Abstract

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We present N-heterocycle-stabilized iodanes (NHIs) as suitable reagents for the mild oxidation of activated alcohols. Two different protocols, both involving activation by chloride additives, were used to synthesize benzylic ketones and aldehydes without overoxidation in up to 97% yield. Based on MS experiments an activated hydroxy(chloro)iodane is proposed as the reactive intermediate.

Keywords