Regioselective formation of 2,5-disubstituted oxazoles via copper(I)-catalyzed cycloaddition of acyl azides and 1-alkynes
The reaction of 1-alkynes with acyl azides in the presence of [Tpm *,BrCu(NCMe)]BF4 [Tpm*,Br = tris(3,5-dimethyl-4-bromopyrazolyl)methane] as the catalyst provides 2,5-oxazoles in moderate to high yields. This is a novel transformation of the CuAAC type that constitutes a significant variation of th...
| Autores: | , , , |
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| Formato: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2011 |
| País: | España |
| Recursos: | Universidad de Sevilla (US) |
| Repositorio: | idUS. Depósito de Investigación de la Universidad de Sevilla |
| OAI Identifier: | oai:idus.us.es:11441/134669 |
| Acesso em linha: | https://hdl.handle.net/11441/134669 https://doi.org/10.1021/ja109732s |
| Access Level: | acceso abierto |
| Resumo: | The reaction of 1-alkynes with acyl azides in the presence of [Tpm *,BrCu(NCMe)]BF4 [Tpm*,Br = tris(3,5-dimethyl-4-bromopyrazolyl)methane] as the catalyst provides 2,5-oxazoles in moderate to high yields. This is a novel transformation of the CuAAC type that constitutes a significant variation of the commonly observed [3 + 2] cycloaddition reaction to yield 1,2,3-triazoles. |
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