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Enantioselective Synthesis of 2-Amino-1,1-diarylalkanes Bearing a Carbocyclic Ring Substituted Indole through Asymmetric Catalytic Reaction of Hydroxyindoles with Nitroalkenes

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Enantioselective Synthesis of 2-Amino-1,1-diarylalkanes Bearing a Carbocyclic Ring Substituted Indole through Asymmetric Catalytic Reaction of Hydroxyindoles with Nitroalkenes

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Vila, C.; Rostoll-Berenguer, J.; Sánchez-García, R.; Blay, G.; Fernandez, I.; Muñoz Roca, MDC.; Pedro, JR. (2018). Enantioselective Synthesis of 2-Amino-1,1-diarylalkanes Bearing a Carbocyclic Ring Substituted Indole through Asymmetric Catalytic Reaction of Hydroxyindoles with Nitroalkenes. The Journal of Organic Chemistry. 83(12):6397-6407. https://doi.org/10.1021/acs.joc.8b00612

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/154384

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Title: Enantioselective Synthesis of 2-Amino-1,1-diarylalkanes Bearing a Carbocyclic Ring Substituted Indole through Asymmetric Catalytic Reaction of Hydroxyindoles with Nitroalkenes
Author: Vila, Carlos Rostoll-Berenguer, Jaume Sánchez-García, Rubén Blay, Gonzalo Fernandez, Isabel Muñoz Roca, María Del Carmen Pedro, Jose R.
UPV Unit: Universitat Politècnica de València. Departamento de Física Aplicada - Departament de Física Aplicada
Issued date:
Abstract:
[EN] An asymmetric catalytic reaction of hydroxyindoles with nitroalkenes leading to the Friedel-Crafts alkylation in the carbocyclic ring of indole is presented. The method is based on the activating/directing effects of ...[+]
Copyrigths: Cerrado
Source:
The Journal of Organic Chemistry. (issn: 0022-3263 )
DOI: 10.1021/acs.joc.8b00612
Publisher:
American Chemical Society
Publisher version: https://doi.org/10.1021/acs.joc.8b00612
Project ID:
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/
Thanks:
Financial support from the MINECO (Gobierno de Espana; CTQ2017-84900-P) is gratefully acknowledged. C.V. thanks MINECO for a JdC contract. J.R.-B. thanks the Ministry of Education for a Collaboration grant. Access to NMR, ...[+]
Type: Artículo

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