4.8 Article

Synthesis of α-CF3-Substituted Carbonyl Compounds with Relative and Absolute Stereocontrol Using Electrophilic CF3-Transfer Reagents

Journal

ORGANIC LETTERS
Volume 13, Issue 21, Pages 5762-5765

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol2023328

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Funding

  1. ETH Zurich
  2. bilateral French-Swiss Germaine de Stael programme

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Evans-type chiral lithium imide enolates undergo diastereoselective alpha-trifluoromethylation with a hypervalent Iodine-CF3 reagent with up to 91% combined Isolated yield and 97:3 dr. The resulting isolated dlastereopure products can be further transformed into valuable products without racemization.

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