4.8 Article

Rh(I)-Catalyzed Asymmetric 1,2-Addition to α-Diketones with Chiral Sulfur-Alkene Hybrid Ligands

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ORGANIC LETTERS
卷 14, 期 2, 页码 624-627

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AMER CHEMICAL SOC
DOI: 10.1021/ol203238j

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  1. National Science Foundation of China [21072194, 21172222]
  2. 973 program [2010CB833300]

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This paper describes a Rh(I)-catalyzed highly efficient and enantioselective 1,2-addition of arylboronic acids to alpha-diketones with the use of a simple sulfur-alkene hybrid ligand. With as low as a 0.1 mol % catalyst loading, a variety of optically active alpha-hydroxyketones can be furnished in high yields with excellent ee's.

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