4.8 Article

Nucleophilic Amination of Methoxy Arenes Promoted by a Sodium Hydride/Iodide Composite

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 56, 期 39, 页码 11807-11811

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201705916

关键词

amination; DFT calculations; nitrogen heterocycles; nucleophilic aromatic substitution; sodium hydride

资金

  1. Nanyang Technological University (NTU)
  2. Singapore Ministry of Education (Academic Research Fund Tier 1) [RG2/15]
  3. Tokyo Biochemical Research Foundation
  4. Tohoku University
  5. Tohoku Kaihatsu Memorial Foundation
  6. Grants-in-Aid for Scientific Research [17J10805, 17H06173] Funding Source: KAKEN

向作者/读者索取更多资源

A method for the nucleophilic amination of methoxy arenes was established by using sodium hydride (NaH) in the presence of lithium iodide (LiI). This method offers an efficient route to benzannulated nitrogen heterocycles. Mechanistic studies showed that the reaction proceeds through an unusual concerted nucleophilic aromatic substitution.

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