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Enaminone ligand-assisted homo- and cross-coupling of terminal alkynes under mild conditions
Copper-catalyzed oxidative coupling reactions of terminal alkynes have been performed at room temperature by using enaminone as effective ligand. Both symmetrical and unsymmetrical 1,3-diynes bearing various functional groups have been synthesized in moderate to excellent yields via homo- and cross-...
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Published in: | Tetrahedron letters 2013-07, Vol.54 (30), p.3953-3955 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Copper-catalyzed oxidative coupling reactions of terminal alkynes have been performed at room temperature by using enaminone as effective ligand. Both symmetrical and unsymmetrical 1,3-diynes bearing various functional groups have been synthesized in moderate to excellent yields via homo- and cross-coupling reactions. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2013.05.063 |