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Merck
  • Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst.

Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst.

Journal of the American Chemical Society (2008-03-07)
Taichi Kano, Mitsuhiro Ueda, Keiji Maruoka
摘要

A direct asymmetric iodination reaction of aldehydes with NIS was found to be catalyzed by the novel axially chiral bifunctional amino alcohol (S)-1d. This method represents the rare example of the catalytic and highly enantioselective synthesis of optically active alpha-iodoaldehydes.

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Sigma-Aldrich
N-碘代琥珀酰亚胺, 95%