Recent advances in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides
Catalytic asymmetric 1,3-dipolar cycloadditions of azomethine ylides have turned out to be one of the most efficient methods for the preparation of enantioenriched pyrrolidines. The past decade has witnessed the development of a bunch of well-defined catalytic systems capable of affording excellent...
| Autores: | , |
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| Formato: | artículo |
| Fecha de publicación: | 2014 |
| País: | España |
| Recursos: | Universidad Autónoma de Madrid |
| Repositorio: | Biblos-e Archivo. Repositorio Institucional de la UAM |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.uam.es:10486/670700 |
| Acesso em linha: | http://hdl.handle.net/10486/670700 https://dx.doi.org/10.1039/C4CC04381B |
| Access Level: | acceso abierto |
| Palavra-chave: | Aldehyde Azomethine ylide Carbonyl derivative Fluorine Fullerene derivative Pyrrolidine derivative Quinone derivative Thiourea Química |
| Resumo: | Catalytic asymmetric 1,3-dipolar cycloadditions of azomethine ylides have turned out to be one of the most efficient methods for the preparation of enantioenriched pyrrolidines. The past decade has witnessed the development of a bunch of well-defined catalytic systems capable of affording excellent diastereo and enantioselectivities. Recently, a great effort has been focused on expanding the scope of the cycloaddition with regard to both reaction partners. In this review, we will discuss important advances that have been reported in this area since 2011 |
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