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Phosphine-Free Palladium Acetate Catalyzed Suzuki Reaction in Water
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Abstract

Pd(OAc)2 in a mixture of water and poly(ethylene glycol) (PEG) is shown to be an extremely active catalyst for the Suzuki reaction of aryl iodides and bromides. The reaction can be conducted under mild conditions (50 °C) without the use of a microwave or phosphine ligand in high yields. The isolation of the products is readily performed by the extraction of diethyl ether, and the Pd(OAc)2−PEG can be reused without significant loss in activity.
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This article has been cited by 17 ACS Journal articles (5 most recent appear below).

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PdEDTA Held in an Ionic Liquid Brush as a Highly Efficient and Reusable Catalyst for Suzuki Reactions in Water
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Jun-Fa Wei, Jiao Jiao, Jin-Juan Feng, Jing Lv, Xi-Ru Zhang, Xian-Ying Shi and Zhan-Guo ChenThe Journal of Organic Chemistry2009 74 (16), 6283-6286An efficient and reusable catalyst with PdEDTA immobilized in an ionic liquid brush and a green procedure have been developed for coupling aryl iodides and bromides with phenylboronic acid. These reactions were conducted in water under aerobic conditions ...

The Garden of Green Organic Chemistry at Hendrix College
Thomas E. Goodwin2009 1011 (), 37-53The Garden of Green Organic Chemistry at Hendrix College
Thomas E. Goodwin2009 1011 (), 37-53The Hendrix College organic chemistry laboratories were converted to microscale experiments in 1988 to minimize possible adverse environmental impact, increase lab safety, and decrease generation of waste and costs of waste disposal. As we became aware of ...
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History
- Published In Issue July 22, 2005
- Received April 12, 2005
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