Abstract
Cu-based catalysts represent a powerful tool for a variety of synthetic transformations, including arylation of nucleophiles, alkyne coupling, dipolar cycloadditions, Diels-Alder reactions, oxidations, condensations and enantioselective reactions. The use of water as reaction medium for these procedures is currently emerging as a very active research field. The present Review focuses on the more synthetically useful “on water” Cu-mediated processes, in which organic co-solvents are absent (or present in negligible amount), and covers the literature until the end of 2009.
Keywords: Copper catalysis, Water, Ullman reaction, Cycloadditions, Oxidations, Enantioselective reactions, dipolar cycloadditions, 2-Dimethylaminoethanol, 2,2'-Biquinoline-4,4'-dicarboxylic acid dipotassium salt, Ethylenediamine, Polyethylene glycol, N,N,N',N'Tetramethylethylenediamine
Current Organic Synthesis
Title: Cu-Mediated Organic Transformations in Water
Volume: 9 Issue: 1
Author(s): Fabio Marinelli
Affiliation:
Keywords: Copper catalysis, Water, Ullman reaction, Cycloadditions, Oxidations, Enantioselective reactions, dipolar cycloadditions, 2-Dimethylaminoethanol, 2,2'-Biquinoline-4,4'-dicarboxylic acid dipotassium salt, Ethylenediamine, Polyethylene glycol, N,N,N',N'Tetramethylethylenediamine
Abstract: Cu-based catalysts represent a powerful tool for a variety of synthetic transformations, including arylation of nucleophiles, alkyne coupling, dipolar cycloadditions, Diels-Alder reactions, oxidations, condensations and enantioselective reactions. The use of water as reaction medium for these procedures is currently emerging as a very active research field. The present Review focuses on the more synthetically useful “on water” Cu-mediated processes, in which organic co-solvents are absent (or present in negligible amount), and covers the literature until the end of 2009.
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Cite this article as:
Marinelli Fabio, Cu-Mediated Organic Transformations in Water, Current Organic Synthesis 2012; 9 (1) . https://dx.doi.org/10.2174/157017912798889134
DOI https://dx.doi.org/10.2174/157017912798889134 |
Print ISSN 1570-1794 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6271 |
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