4.6 Article

Formation of Quaternary Chiral Centers by N-Heterocyclic Carbene-Cu-Catalyzed Asymmetric Conjugate Addition Reactions with Grignard Reagents on Trisubstituted Cyclic Enones

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 16, 期 32, 页码 9890-9904

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201000471

关键词

asymmetry; conjugate addition; copper; Grignard reaction; N-heterocyclic carbenes

资金

  1. Swiss National Research Foundation [200020-126663]
  2. COST action D40 [C07 0097]

向作者/读者索取更多资源

The copper-catalyzed conjugate addition of Grignard reagents to 3-substituted cyclic enones allows the formation of all-carbon chiral quaternary centers We demonstrate in this article that N-heterocyclic carbencs act as efficient chiral ligands for this transformation High enantioselectivities (up to 96% ee) could be obtained for a variety of substrates

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