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Asymmetric tandem Michael addition/oxidation of pyrazolones with p-benzoquinone catalyzed by cinchona alkaloids

期刊

TETRAHEDRON-ASYMMETRY
卷 26, 期 23, 页码 1382-1387

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2015.10.006

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资金

  1. National Natural Science Foundation of China [21076035, 20972022]
  2. Program for New Century Excellent Talents in University [NCET-11-0053]
  3. Fundamental Research Funds of the Central Universities [DUT13ZD202]

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By employing a natural cinchona alkaloid as a catalyst, the enantioselective tandem Michael addition/oxidation of 4-substituted pyrazol-5-ones with p-benzoquinones was realized. The reaction afforded a wide range of 4,4-disubstituted pyrazol-5-ones with moderate to good yields (up to 72%) and moderate to good enantioselectivities (up to 99%). (C) 2015 Elsevier Ltd. All rights reserved.

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