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...
Published in: | The Journal of Organic Chemistry |
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Online Access: | http://hdl.handle.net/10045/38257 https://doi.org/10.1021/jo400522m |
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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 |
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Open Polar |
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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 |
_version_ |
1766161555973472256 |