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Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Dereved Nitroalkenes

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Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Dereved Nitroalkenes

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Vila, C.; Dharmaraj, NR.; Faubel, A.; Blay, G.; Cardona, ML.; Muñoz Roca, MDC.; Pedro, JR. (2019). Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Dereved Nitroalkenes. European Journal of Organic Chemistry. (19):3040-3044. https://doi.org/10.1002/ejoc.201900328

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/139151

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Título: Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Dereved Nitroalkenes
Autor: Vila, C. Dharmaraj, N. R. Faubel, A. Blay, G. Cardona, M. L. Muñoz Roca, María Del Carmen Pedro, J. R.
Entidad UPV: Universitat Politècnica de València. Departamento de Física Aplicada - Departament de Física Aplicada
Fecha difusión:
Resumen:
[EN] Hydroquinine 2,5-diphenyl-4,6-pyrimidinediyl diether [(DHQ)(2)Pyr] catalyzed the regio-, diastereo-, and enantioselective addition of 4-substituted pyrazolones to isatin-derived nitroalkenes, providing a variety of ...[+]
Palabras clave: Asymmetric catalysis , Nitroalkenes , Pyrazolones , Organocatalysis , Nucleophilic substitution
Derechos de uso: Reserva de todos los derechos
Fuente:
European Journal of Organic Chemistry. (issn: 1434-193X )
DOI: 10.1002/ejoc.201900328
Editorial:
John Wiley & Sons
Versión del editor: https://doi.org/10.1002/ejoc.201900328
Código del Proyecto:
info:eu-repo/grantAgreement/MINECO//RYC-2016-20187/
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-84900-P/ES/REACCIONES DE ADICION ENANTIOSELECTIVAS MEDIANTE SISTEMAS MULTICATALITICOS. HERRAMIENTAS PARA LA SINTESIS EFICIENTE DE MOLECULAS CON ACTIVIDAD FARMACOLOGICA/
Descripción: This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Agradecimientos:
Financial support from the Agencia Estatal de Investigacion (AEI, Spanish Government) and Fondo Europeo de Desarrollo Regional (FEDER, European Union) (CTQ2017-84900-P) is acknowledged. C. V. thanks the Spanish Government ...[+]
Tipo: Artículo

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