Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2006(10): 1045-1045
DOI: 10.1055/s-2006-949308
DOI: 10.1055/s-2006-949308
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York
Reductive Carboamination of Olefins with Aryldiazonium Salts
M. R. Heinrich*, O. Blank, S. Wölfel
Technische Universität München, Garching, Germany
Further Information
Publication History
Publication Date:
21 September 2006 (online)

Significance
Although the use of diazonium salts in the addition reaction to olefins has been known for a long time, this process was limited to electron-deficient alkenes. The authors developed for the first time a procedure which allows the functionalization of non-activated terminal alkenes bearing functional groups. This is a very simple and elegant method, allowing the fast assembly of complex polyfunctional molecules starting from inexpensive substituted anilines. Obviously, this method will soon find a broad application in the synthesis of biologically active compounds.