4.8 Article

Asymmetric Lewis Acid Mediated [1,2]-Rearrangement of Proline-Derived Ammonium Ylides

Journal

ORGANIC LETTERS
Volume 11, Issue 4, Pages 919-921

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol8028803

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Funding

  1. Royal Institute of Technology
  2. Swedish Research Council
  3. Knut and Alice Wallenberg foundation

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The first example of asymmetric Lewis acid mediated [1,2]-rearrangement of N-benzylic proline amides to form quaternary proline derivatives is reported. The presented reaction is shown to proceed with remarkable high C-N-C chirality transfer. Various quaternary proline derivatives have been prepared in good to excellent yields and high enantiomeric purity.

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