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Hydroxy-Directed Enantioselective Hydroxyalkylation in the Carbocyclic Ring of Indoles

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Hydroxy-Directed Enantioselective Hydroxyalkylation in the Carbocyclic Ring of Indoles

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Montesinos-Magraner, M.; Vila, C.; Blay, G.; Fernández, I.; Muñoz Roca, MDC.; Pedro, J. (2017). Hydroxy-Directed Enantioselective Hydroxyalkylation in the Carbocyclic Ring of Indoles. Organic Letters. 19(7):1546-1549. https://doi.org/10.1021/acs.orglett.7b00354

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/140846

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Title: Hydroxy-Directed Enantioselective Hydroxyalkylation in the Carbocyclic Ring of Indoles
Author: Montesinos-Magraner, M. Vila, C. Blay, G. Fernández, I. Muñoz Roca, María Del Carmen Pedro, J.R.
UPV Unit: Universitat Politècnica de València. Departamento de Física Aplicada - Departament de Física Aplicada
Issued date:
Abstract:
[EN] A Cinchona-derived squaramide catalyzes the reaction between hydroxyindoles and isatins leading to enantioenriched indoles substituted in the carbocyclic ring. The reaction proceeds efficiently with differently ...[+]
Copyrigths: Cerrado
Source:
Organic Letters. (issn: 1523-7060 )
DOI: 10.1021/acs.orglett.7b00354
Publisher:
American Chemical Society
Publisher version: https://doi.org/10.1021/acs.orglett.7b00354
Project ID:
info:eu-repo/grantAgreement/MINECO//CTQ2013-47494-P/ES/NUEVOS RETOS EN EL DESARROLLO DE PROCESOS ENANTIOSELECTIVOS DE FORMACION DE ENLACES C-C MEDIANTE CATALISIS DUAL COOPERATIVA./
Thanks:
Financial support from MINECO (Gobierno de Espana; CTQ2013-47494-P). M.M-M. thanks Universitat de Valencia for a predoctoral grant, and C.V. thanks MINECO for a JdC contract. Access to NMR and MS facilities from the SCSIE-UV.[+]
Type: Artículo

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