4.0 Article

Ionic liquid-supported proline as catalyst in direct asymmetric aldol reaction

Journal

RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 44, Issue 12, Pages 1807-1810

Publisher

MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S1070428008120154

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Funding

  1. Natural Science Foundation of China [20 862 004]
  2. Key Project of Science and Technology of Guizhou province [2007-2022]
  3. Special Scientific Research Foundation of Guizhou [TZJF-2006.25]

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Ionic-liquid-supported proline derivative was synthesized starting from L-proline and was used to catalyze direct asymmetric aldol reaction of acetone with aldehydes. The yield and optical purity of the condensation products, the corresponding beta-hydroxy carbonyl compounds were comparable with those obtained under homogeneous conditions. Moreover, the catalyst can be reused for at least four times.

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