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Synthesis 2010(1): 85-90
DOI: 10.1055/s-0029-1217082
DOI: 10.1055/s-0029-1217082
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of 2,2′-Bipyridines via Suzuki-Miyaura Cross-Coupling
Further Information
Received
26 August 2009
Publication Date:
26 October 2009 (online)
Publication History
Publication Date:
26 October 2009 (online)
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Abstract
For a long time, the Suzuki-Miyaura cross-coupling reaction could not be used for the synthesis of 2,2′-bipyridines due to the lack of sufficiently stable 2-pyridylboron compounds. Stabilized 2-pyridylboronic acid esters recently developed by Hodgson, however, were found to be ideally suited for this purpose. Two general protocols could be developed and demonstrated to be valuable alternatives, which can be used very efficiently for the synthesis of functionalized 2,2′-bipyridines.
Key words
cross-coupling reactions - bipyridines - palladium - 2-pyridylboronic acid esters - Suzuki-Miyaura reaction
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