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Solvent-free Suzuki and Stille cross-coupling reactions of 4- and 5-halo-1,2,3-triazoles
[Display omitted] An environmentally friendly and efficient synthesis of fully substituted 1,2,3-triazoles comprises solvent-free palladium-catalyzed Suzuki cross-coupling of halo-1,2,3-triazoles with pinacol arylboronates. The efficiencies of Stille and Suzuki reactions with halotriazoles under sol...
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Published in: | Mendeleev communications 2019-03, Vol.29 (2), p.147-149 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
An environmentally friendly and efficient synthesis of fully substituted 1,2,3-triazoles comprises solvent-free palladium-catalyzed Suzuki cross-coupling of halo-1,2,3-triazoles with pinacol arylboronates. The efficiencies of Stille and Suzuki reactions with halotriazoles under solvent-free conditions were compared. |
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ISSN: | 0959-9436 |
DOI: | 10.1016/j.mencom.2019.03.009 |