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Synthesis 2009(18): 3150-3156
DOI: 10.1055/s-0029-1216905
DOI: 10.1055/s-0029-1216905
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Efficient Microwave-Assisted Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions in 5-Nitroimidazole Series
Further Information
Received
6 May 2009
Publication Date:
14 July 2009 (online)
Publication History
Publication Date:
14 July 2009 (online)

Abstract
A new simple, rapid and high yielding synthesis (mean yield = 83%) of various 4-aryl, 4-heteroaryl, and 4-styryl-1,2-dimethyl-5-nitro-1H-imidazoles by palladium-catalyzed Suzuki-Miyaura cross-coupling reactions using microwave irradiation is described.
Key words
cross-coupling - 5-nitroimidazoles - palladium - Suzuki reaction - arylations
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References
Detailed X-ray crystallographic data are available from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2, 1EZ, UK; fax: +44 (1223)336033; email: deposit@ccdc.cam.ac.uk. (compound 20: CCDC # 704224 and compound 21: CCDC # 716232). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.