4.8 Article

Access to Oxoquinoline Heterocycles by N-Heterocyclic Carbene Catalyzed Ester Activation for Selective Reaction with an Enone

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 25, 页码 6506-6510

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201402620

关键词

C-H activation; cyclization; heterocycles; N-heterocyclic carbene; organocatalysis

资金

  1. Singapore National Research Foundation (NRF)
  2. Singapore Economic Development Board (EDB)
  3. GlaxoSmithKline (GSK)
  4. Nanyang Technological University (NTU)
  5. National Research Foundation [NRF-CRP4-2008-02]

向作者/读者索取更多资源

Organocatalytic ester activation is developed for a highly selective cascade reaction between saturated esters and amino enones. The reaction involves activation of the b-carbon atom of the ester as a key step. This method allows a single-step access to multicyclic oxoquinoline-type heterocycles with high enantiomeric ratios.

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