Enantio and Diastereoselective Addition of Phenylacetylene to Racemic α-chloroketones

In this report, we have presented the first diastereoselective addition of phenylacetylene to chiral racemic chloroketones. The addition is controlled by the reactivity of the chloroketones that allowed the stereoselective reaction to be performed at –20 °C. Chiral racemic chloroketones are used in...

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Detalles Bibliográficos
Autores principales: Alesi, Silvia, Emer, Enrico, Capdevila, Montse Guiteras, Petruzziello, Diego, Gualandi, Andrea, Cozzi, Pier Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264675/
https://www.ncbi.nlm.nih.gov/pubmed/21701439
http://dx.doi.org/10.3390/molecules16065298

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264675/
https://www.ncbi.nlm.nih.gov/pubmed/21701439
http://dx.doi.org/10.3390/molecules16065298

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