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Holmquist, M.; Blay, G.; Muñoz Roca, MDC.; Pedro, JR. (2014). Enantioselective Addition of Nitromethane to 2-Acylpyridine N-Oxides. Expanding the Generation of Quaternary Stereocenters with the Henry Reaction. Organic Letters. 16(4):1204-1207. https://doi.org/10.1021/ol500082d
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/150433
Título: | Enantioselective Addition of Nitromethane to 2-Acylpyridine N-Oxides. Expanding the Generation of Quaternary Stereocenters with the Henry Reaction | |
Autor: | Holmquist, M. Blay, G. Pedro, J. R. | |
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[EN] The direct asymmetric Henry reaction with prochiral ketones, leading to tertiary nitroaldols, is an elusive reaction so far limited to a reduced number of reactive substrates such as trifluoromethyl ketones or alpha-keto ...[+]
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Derechos de uso: | Cerrado | |
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Versión del editor: | https://doi.org/10.1021/ol500082d | |
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Financial support from the Ministerio de Economia y Competitividad (Gobierno de Espana) and FEDER (EU) (CTQ2009-13083) and from Generalitat Valenciana (ACOMP2012-212 and ISIC 2012/001) is acknowledged. M.H. thanks the GV ...[+]
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