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Synthesis 2004(5): 683-691
DOI: 10.1055/s-2004-816004
DOI: 10.1055/s-2004-816004
PAPER
© Georg Thieme Verlag Stuttgart · New York
Zinc-Mediated Radical Reactions of Per- (or Poly)fluorophenyl Aromatic Aldimines in Aqueous Media
Further Information
Received
2 November 2003
Publication Date:
09 March 2004 (online)
Publication History
Publication Date:
09 March 2004 (online)
![](https://www.thieme-connect.de/media/synthesis/200405/lookinside/thumbnails/10.1055-s-2004-816004-1.jpg)
Abstract
The intermolecular additions of alkyl halides to per- (or poly)fluorophenyl aromatic aldimines using zinc as a single-electron-transfer radical initiator have been studied in aqueous media. The reaction proceeds well for imines with different substituents at room temperature under air atmosphere and the corresponding fluorine-containing amines and 1,2-diamines are obtained in poor to good yields. A tentative reaction mechanism is proposed.
Key words
polyfluororinated amines - imines - zinc - alkyl halides - radical reactions
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