4.6 Article

Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 22, Issue 12, Pages 4030-4035

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201504844

Keywords

alkenes; arylation; hypervalent iodine; oxidation; rearrangement

Funding

  1. EPSRC [EP/J00569X/1]
  2. EU [621956]
  3. School of Chemistry, Cardiff University
  4. EPSRC [EP/J00569X/1] Funding Source: UKRI
  5. Engineering and Physical Sciences Research Council [EP/J00569X/1] Funding Source: researchfish

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A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes has been developed. This practically simple protocol provides access to enantioenriched -arylated ketones without the use of transition metals from readily accessible alkenes.

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