Citation: Xiao Ya YUAN, Hai Yan LI, Zheng Pu ZHANG, P. HODGE. Immobilizing BINOL via Suzuki Reaction: Synthesis and Application in Catalytic Asymmetric Oxidation of Sulfide to Sulfoxide[J]. Chinese Chemical Letters, ;2006, 17(7): 911-912.
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Immobilizing chiral 1,1'-bi-2-naphthol (BINOL) in one step onto polymer backbone via stable carbon-carbon bond through Suzuki reaction was achieved. The application of this immobilized chiral BINOL to the catalytic asymmetric oxidation of sulfide to sulfoxide exhibited good activity (up to 60% yield) and high enantioselectivity (up to 89% ee). The immobilized chiral catalyst was very stable and could be readily reused for over 5 times without significant loss of catalytic activity and enantioselectivity.
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Keywords:
- 1,1'-Bi-2-naphthol,
- asymmetric catalysis,
- immobilization,
- sulfoxide
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