Adelaide Research & Scholarship
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https://hdl.handle.net/2440/4594
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| Type: | Journal article |
| Title: | Palladium-catalysed coupling of terminal alkynes with aryl halides aided by catalytic zinc |
| Author: | Crisp, Geoffrey T. Turner, Peter David Stephens, Kim A. |
| Citation: | Journal of Organometallic Chemistry, 1998; 570(2):219-224 |
| Issue Date: | 1998 |
| ISSN: | 0022-328X |
| School/Discipline: | School of Chemistry and Physics : Chemistry |
| Statement of Responsibility: | Geoffrey T Crisp, Peter D Turner, Kim A Stephens |
| Abstract: | The palladium-catalysed coupling of aryl halides with terminal alkynes can be performed using base, zinc chloride and sodium iodide. This protocol represents a convenient method for the generation of nucleophilic acetylides in situ. |
| Keywords: | Palladium catalysis; Coupling of oxyhalides with alkynes; Nucleophilic alkynes |
| Rights: | Copyright © 1998 Elsevier Science S.A. All rights reserved. |
| DOI: | 10.1016/S0022-328X(98)00765-7 |
| Appears in Collections: | Chemistry publications |
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