4.4 Article

Highly enantioselective Michael addition of malononitrile to α,β-unsaturated pyrazolamides catalyzed by a bifunctional thiourea

期刊

TETRAHEDRON
卷 72, 期 7, 页码 973-978

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2015.12.067

关键词

Enantioselective; Michael addition; Malononitrile; alpha,beta-Unsaturated pyrazolamide; Bifunctional thiourea

资金

  1. National Natural Science Foundation of China [21402163]
  2. Department of Science and Technology of Sichuan Province [2013JY0135]
  3. Project of Postgraduate Degree Construction, Southwest University for Nationalities [2015XWD-S0703]

向作者/读者索取更多资源

A new protocol for the organocatalytic asymmetric Michael addition of malononitrile to alpha,beta-unsaturated pyrazolamides is reported. The Michael reaction proceeded smoothly in the presence of a bifunctional thiourea and provided the desired adducts in moderate to excellent yields (27-99%) and good to excellent enantioselectivities (80-95% ee). (C) 2015 Elsevier Ltd. All rights reserved.

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