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A New Biarylphosphine Ligand for the Pd-Catalyzed Synthesis of Diaryl Ethers under Mild Conditions

Author(s)
Salvi, Luca; Ali, Siraj Z.; Davis, Nicole Rose; Buchwald, Stephen Leffler
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.

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Abstract
A new bulky biarylphosphine ligand (L8) has been developed that allows the Pd-catalyzed C–O cross-coupling of a wide range of aryl halides and phenols under milder conditions than previously possible. A direct correlation between the size of the ligand substituents in the 2′, 4′, and 6′ positions of the nonphosphine containing ring and the reactivity of the derived catalyst system was observed. Specifically, the rate of coupling increased with the size of these substituents.
Date issued
2011-12
URI
http://hdl.handle.net/1721.1/81974
Department
Massachusetts Institute of Technology. Department of Chemistry
Journal
Organic Letters
Publisher
American Chemical Society (ACS)
Citation
Salvi, Luca, Nicole R. Davis, Siraj Z. Ali, and Stephen L. Buchwald. “A New Biarylphosphine Ligand for the Pd-Catalyzed Synthesis of Diaryl Ethers under Mild Conditions.” Organic Letters 14, no. 1 (January 6, 2012): 170-173.
Version: Author's final manuscript
ISSN
1523-7060
1523-7052

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