4.8 Article

Sulfoxide-Alkene Hybrids: A New Class of Chiral Ligands for the Hayashi-Miyaura Reaction

Journal

ORGANIC LETTERS
Volume 13, Issue 12, Pages 3182-3185

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol200841x

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Funding

  1. European Research Council under the European Community [FP7/2007-2013]
  2. ERC [227763]
  3. Alexander von Humboldt Foundation
  4. European Research Council (ERC) [227763] Funding Source: European Research Council (ERC)

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Sulfoxide-alkene hybrids are introduced as a new class of chiral heterodentate ligands for the Hayashi-Miyaura reaction. The synthesis of these ligands was achieved without the use of protecting groups. A chiral resolution was performed via simple column-chromatographic separation of the diastereomeric ligands. Both diastereomers proved to be excellent ligands In Rh-catalyzed 1,4-addition reactions, furnishing chiral Products with high enantloselectivities and, remarkably, opposite stereoconfigurations.

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