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Synthesis 2011(10): 1581-1586
DOI: 10.1055/s-0030-1260009
DOI: 10.1055/s-0030-1260009
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Biaryl Derivatives by Using Ruthenium-Mediated [2+2+2] Cyclotrimerization and Suzuki-Miyaura Cross-Coupling as Key Steps
Further Information
Received
10 February 2011
Publication Date:
19 April 2011 (online)
Publication History
Publication Date:
19 April 2011 (online)
Abstract
Functionalized biaryl derivatives have been prepared by applying [2+2+2] cyclotrimerization with the aid of Grubbs’ first-generation catalyst (G-I). The trimerized products were subjected to the Suzuki-Miyaura cross-coupling reaction sequence to generate highly functionalized biaryl derivatives.
Key words
terphenyl - quinquephenyl - [2+2+2] cyclotrimerization - Suzuki-Miyaura cross-coupling - metathesis
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References
CCDC-797048 (7b) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.