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Synthesis 2008(3): 474-478
DOI: 10.1055/s-2008-1032027
DOI: 10.1055/s-2008-1032027
PAPER
© Georg Thieme Verlag Stuttgart · New York
Palladium-Catalyzed Cross-Coupling Alkylation of Arenediazonium o-Benzenedisulfonimides
Further Information
Received
24 October 2007
Publication Date:
10 January 2008 (online)
Publication History
Publication Date:
10 January 2008 (online)
Abstract
Arenediazonium o-benzenedisulfonimides were reacted with tetramethyltin, tetrabutyltin or trialkylboranes. The reactions, carried out in the presence of palladium(II) derivatives as precatalysts, gave the methylation and alkylation products with good overall conversions. The o-benzenedisulfonimide was recovered in high yield from all the reactions and could be recycled for the preparation of other salts.
Key words
palladium - Stille reaction - Suzuki reaction - cross-coupling - diazo compounds
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