Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts

Wet unsupported and supported 1,1′-binaphthalene-2,2′-diamine (BINAM) derived prolinamides are efficient organocatalysts under solvent-free conditions at room temperature to perform the synthesis of chiral tacrine analogues in good yields (up to 93%) and excellent enantioselectivies (up to 96%). The...

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Published in:The Journal of Organic Chemistry
Main Authors: Bañón Caballero, Abraham, Guillena, Gabriela, Nájera, Carmen
Other Authors: Universidad de Alicante. Departamento de Química Orgánica, Universidad de Alicante. Instituto Universitario de Síntesis Orgánica, Catálisis Estereoselectiva en Síntesis Orgánica (CESO), Síntesis Asimétrica (SINTAS)
Format: Article in Journal/Newspaper
Language:English
Published: American Chemical Society 2013
Subjects:
Online Access:http://hdl.handle.net/10045/38257
https://doi.org/10.1021/jo400522m
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spelling ftunivalicante:oai:rua.ua.es:10045/38257 2023-05-15T17:53:51+02:00 Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts Bañón Caballero, Abraham Guillena, Gabriela Nájera, Carmen Universidad de Alicante. Departamento de Química Orgánica Universidad de Alicante. Instituto Universitario de Síntesis Orgánica Catálisis Estereoselectiva en Síntesis Orgánica (CESO) Síntesis Asimétrica (SINTAS) 2013-05-10 http://hdl.handle.net/10045/38257 https://doi.org/10.1021/jo400522m eng eng American Chemical Society http://dx.doi.org/10.1021/jo400522m Journal of Organic Chemistry. 2013, 78(11): 5349-5356. doi:10.1021/jo400522m 0022-3263 (Print) 1520-6904 (Online) http://hdl.handle.net/10045/38257 doi:10.1021/jo400522m © 2013 American Chemical Society info:eu-repo/semantics/openAccess Solvent-free Enantioselective Friedländer condensation Wet 1,1′-binaphthalene-2,2′-diamine-derived prolinamides Organocatalysis Química Orgánica info:eu-repo/semantics/article 2013 ftunivalicante https://doi.org/10.1021/jo400522m 2020-06-05T13:08:40Z Wet unsupported and supported 1,1′-binaphthalene-2,2′-diamine (BINAM) derived prolinamides are efficient organocatalysts under solvent-free conditions at room temperature to perform the synthesis of chiral tacrine analogues in good yields (up to 93%) and excellent enantioselectivies (up to 96%). The Friedländer reaction involved in this process takes place with several cyclohexanone derivatives and 2-aminoaromatic aldehydes, and it is compatible with the presence of either electron-withdrawing or electron-donating groups at the aromatic ring of the 2-aminoaryl aldehyde derivatives used as electrophiles. The reaction can be extended to cyclopentanone derivatives, affording a regioisomeric but separable mixture of products. The use of the wet silica gel supported organocatalyst, under solvent-free conditions, for this process led to the expected product (up to 87% enantiomeric excess), with its reuse being possible at least up to five times. This work was financially supported by the Ministerio de Ciencia e Innovación (MICINN: Projects: CTQ2010-20387 and Consolider Ingenio 2010 CSD2007-00006), the Generalitat Valenciana (Prometeo/2009/039, the University of Alicante and the EU (ORCA action CM0905). A.B.-C. thanks the Spanish MICINN for a predoctoral fellowship (FPU AP2009-3601). Article in Journal/Newspaper Orca RUA - Repositorio Institucional de la Universidad de Alicante The Journal of Organic Chemistry 78 11 5349 5356
institution Open Polar
collection RUA - Repositorio Institucional de la Universidad de Alicante
op_collection_id ftunivalicante
language English
topic Solvent-free
Enantioselective
Friedländer condensation
Wet 1,1′-binaphthalene-2,2′-diamine-derived prolinamides
Organocatalysis
Química Orgánica
spellingShingle Solvent-free
Enantioselective
Friedländer condensation
Wet 1,1′-binaphthalene-2,2′-diamine-derived prolinamides
Organocatalysis
Química Orgánica
Bañón Caballero, Abraham
Guillena, Gabriela
Nájera, Carmen
Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts
topic_facet Solvent-free
Enantioselective
Friedländer condensation
Wet 1,1′-binaphthalene-2,2′-diamine-derived prolinamides
Organocatalysis
Química Orgánica
description Wet unsupported and supported 1,1′-binaphthalene-2,2′-diamine (BINAM) derived prolinamides are efficient organocatalysts under solvent-free conditions at room temperature to perform the synthesis of chiral tacrine analogues in good yields (up to 93%) and excellent enantioselectivies (up to 96%). The Friedländer reaction involved in this process takes place with several cyclohexanone derivatives and 2-aminoaromatic aldehydes, and it is compatible with the presence of either electron-withdrawing or electron-donating groups at the aromatic ring of the 2-aminoaryl aldehyde derivatives used as electrophiles. The reaction can be extended to cyclopentanone derivatives, affording a regioisomeric but separable mixture of products. The use of the wet silica gel supported organocatalyst, under solvent-free conditions, for this process led to the expected product (up to 87% enantiomeric excess), with its reuse being possible at least up to five times. This work was financially supported by the Ministerio de Ciencia e Innovación (MICINN: Projects: CTQ2010-20387 and Consolider Ingenio 2010 CSD2007-00006), the Generalitat Valenciana (Prometeo/2009/039, the University of Alicante and the EU (ORCA action CM0905). A.B.-C. thanks the Spanish MICINN for a predoctoral fellowship (FPU AP2009-3601).
author2 Universidad de Alicante. Departamento de Química Orgánica
Universidad de Alicante. Instituto Universitario de Síntesis Orgánica
Catálisis Estereoselectiva en Síntesis Orgánica (CESO)
Síntesis Asimétrica (SINTAS)
format Article in Journal/Newspaper
author Bañón Caballero, Abraham
Guillena, Gabriela
Nájera, Carmen
author_facet Bañón Caballero, Abraham
Guillena, Gabriela
Nájera, Carmen
author_sort Bañón Caballero, Abraham
title Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts
title_short Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts
title_full Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts
title_fullStr Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts
title_full_unstemmed Solvent-Free Enantioselective Friedländer Condensation with Wet 1,1′-Binaphthalene-2,2′-diamine-Derived Prolinamides as Organocatalysts
title_sort solvent-free enantioselective friedländer condensation with wet 1,1′-binaphthalene-2,2′-diamine-derived prolinamides as organocatalysts
publisher American Chemical Society
publishDate 2013
url http://hdl.handle.net/10045/38257
https://doi.org/10.1021/jo400522m
genre Orca
genre_facet Orca
op_relation http://dx.doi.org/10.1021/jo400522m
Journal of Organic Chemistry. 2013, 78(11): 5349-5356. doi:10.1021/jo400522m
0022-3263 (Print)
1520-6904 (Online)
http://hdl.handle.net/10045/38257
doi:10.1021/jo400522m
op_rights © 2013 American Chemical Society
info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.1021/jo400522m
container_title The Journal of Organic Chemistry
container_volume 78
container_issue 11
container_start_page 5349
op_container_end_page 5356
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