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New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction

New L-serine derivative ligands were prepared and tested as cocatalyst in the Diels-Alder reactions between cyclopentadiene (CPD) and methyl acrylate, in the presence of several Lewis acids. The catalytic potential of the in situ formed complexes was evaluated based on the reaction yield. Bidentate...

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Autores principales: Sousa, Carlos A. D., Rodríguez-Borges, José E., Freire, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870085/
https://www.ncbi.nlm.nih.gov/pubmed/24383009
http://dx.doi.org/10.1155/2013/217675
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author Sousa, Carlos A. D.
Rodríguez-Borges, José E.
Freire, Cristina
author_facet Sousa, Carlos A. D.
Rodríguez-Borges, José E.
Freire, Cristina
author_sort Sousa, Carlos A. D.
collection PubMed
description New L-serine derivative ligands were prepared and tested as cocatalyst in the Diels-Alder reactions between cyclopentadiene (CPD) and methyl acrylate, in the presence of several Lewis acids. The catalytic potential of the in situ formed complexes was evaluated based on the reaction yield. Bidentate serine ligands showed good ability to coordinate medium strength Lewis acids, thus boosting their catalytic activity. The synthesis of the L-serine ligands proved to be highly efficient and straightforward.
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spelling pubmed-38700852014-01-01 New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction Sousa, Carlos A. D. Rodríguez-Borges, José E. Freire, Cristina ISRN Org Chem Research Article New L-serine derivative ligands were prepared and tested as cocatalyst in the Diels-Alder reactions between cyclopentadiene (CPD) and methyl acrylate, in the presence of several Lewis acids. The catalytic potential of the in situ formed complexes was evaluated based on the reaction yield. Bidentate serine ligands showed good ability to coordinate medium strength Lewis acids, thus boosting their catalytic activity. The synthesis of the L-serine ligands proved to be highly efficient and straightforward. Hindawi Publishing Corporation 2013-12-05 /pmc/articles/PMC3870085/ /pubmed/24383009 http://dx.doi.org/10.1155/2013/217675 Text en Copyright © 2013 Carlos A. D. Sousa et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sousa, Carlos A. D.
Rodríguez-Borges, José E.
Freire, Cristina
New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction
title New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction
title_full New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction
title_fullStr New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction
title_full_unstemmed New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction
title_short New L-Serine Derivative Ligands as Cocatalysts for Diels-Alder Reaction
title_sort new l-serine derivative ligands as cocatalysts for diels-alder reaction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870085/
https://www.ncbi.nlm.nih.gov/pubmed/24383009
http://dx.doi.org/10.1155/2013/217675
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