4.5 Article

Continuous flow photolysis of aryl azides: Preparation of 3H-azepinones

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 7, 期 -, 页码 1124-1129

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.7.129

关键词

azepinones; azides; continuous flow; nitrenes; photochemistry

资金

  1. Max Planck Society
  2. AstraZeneca RD
  3. Macclesfield, UK
  4. Fonds de Recherche sur la Nature et les Technologies, Quebec

向作者/读者索取更多资源

Photolysis of aryl azides to give nitrenes, and their subsequent rearrangement in the presence of water to give 3H-azepinones, is performed in continuous flow in a photoreactor constructed of fluorinated ethylene polymer (FEP) tubing. Fine tuning of the reaction conditions using the flow reactor allowed minimization of secondary photochemical reactions.

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