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Enantioselective intramolecular (2+2)-photocycloaddition reactions of 4-substituted quinolones catalyzed by a chiral sensitizer with a hydrogen-bonding motif

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Enantioselective intramolecular (2+2)-photocycloaddition reactions of 4-substituted quinolones catalyzed by a chiral sensitizer with a hydrogen-bonding motif

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Müler, C.; Bauer, A.; Maturi, MM.; Cuquerella Alabort, MC.; Miranda Alonso, MÁ.; Bach, T. (2011). Enantioselective intramolecular (2+2)-photocycloaddition reactions of 4-substituted quinolones catalyzed by a chiral sensitizer with a hydrogen-bonding motif. Journal of the American Chemical Society. 133:16689-16697. doi:10.1021/ja207480q.

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/29275

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Título: Enantioselective intramolecular (2+2)-photocycloaddition reactions of 4-substituted quinolones catalyzed by a chiral sensitizer with a hydrogen-bonding motif
Autor:
Entidad UPV: Universitat Politècnica de València. Departamento de Química - Departament de Química
Fecha difusión:
Resumen:
Six 2-quinolones, which bear a terminal alkene linked by a three- or four-membered tether to carbon atom C4 of the quinolone, were synthesized and subjected to an intramolecular [2 + 2]-photocycloaddition. The reaction ...[+]
Derechos de uso: Cerrado
Fuente:
Journal of the American Chemical Society. (issn: 0002-7863 )
DOI: 10.1021/ja207480q
Editorial:
American Chemical Society
Versión del editor: http://dx.doi.org/10.1021/ja207480q
Patrocinador:
Deutsche Forschungsgemeinschaft (DFG) in Germany GRK 1626
Spanish Government CTQ2009-13699
Tipo: Artículo

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