4.8 Article

Catalytic Synthesis of N-Unprotected Piperazines, Morpholines, and Thiomorpholines from Aldehydes and SnAP Reagents

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 54, 期 37, 页码 10884-10888

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201505167

关键词

aldehydes; cross-coupling; homogeneous catalysis; nitrogen heterocycles; SnAP reagents

资金

  1. ETH Research Grant [ETH-12 11-1]
  2. European Research Council (ERC) [306793]
  3. European Research Council (ERC) [306793] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Commercially available SnAP (stannyl amine protocol) reagents allow the transformation of aldehydes and ketones into a variety of N-unprotected heterocycles. By identifying new ligands and reaction conditions, a robust catalytic variant that expands the substrate scope to previously inaccessible heteroaromatic substrates and new substitution patterns was realized. It also establishes the basis for a catalytic enantioselective process through the use of chiral ligands.

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