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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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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. |
format | Online Article Text |
id | pubmed-3870085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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