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Lipshutz, B.H.; Taft, B.R.; Abela, A.R.; Ghorai, S.; Krasovskiy, A.; Duplais, C. |
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Title |
Catalysis in the service of green chemistry: Nobel prize-winning palladium-catalysed cross-couplings, run in water at room temperature |
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Journal Article |
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2012 |
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Platinum Metals Review |
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Platinum Met. Rev. |
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56 |
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2 |
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62-74 |
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Abstract |
Palladium-catalysed cross-couplings, in particular Heck, Suzuki-Miyaura and Negishi reactions developed over three decades ago, are routinely carried out in organic solvents. However, alternative media are currently of considerable interest given an increasing emphasis on making organic processes 'greener'; for example, by minimising organic waste in the form of organic solvents. Water is the obvious leading candidate in this regard. Hence, this review focuses on the application of micellar catalysis, in which a 'designer' surfactant enables these award-winning coupling reactions to be run in water at room temperature. © 2012 Johnson Matthey. |
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UMR-CNRS Ecofog, Institut Pasteur de la Guyane, 23 Avenue Pasteur, 97306 Cayenne, France |
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00321400 (Issn) |
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Cited By (since 1996): 1; Export Date: 15 May 2012; Source: Scopus; Coden: Ptmra; doi: 10.1595/147106712X629761; Language of Original Document: English; Correspondence Address: Lipshutz, B.H.; Department of Chemistry, University of California, Santa Barbara, CA 93106, United States; email: lipshutz@chem.ucsb.edu |
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EcoFoG @ webmaster @ |
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400 |
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