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Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction
Chiral polymeric particles (CPPs) were studied extensively in recent years due to their importance in pharmaceutical applications. Here, nanosized CPPs were synthesized and applied as catalysts for direct asymmetric aldol reaction. The CPPs were prepared by miniemulsion or inverse miniemulsion based...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817469/ https://www.ncbi.nlm.nih.gov/pubmed/36688059 http://dx.doi.org/10.1039/d2ra07244k |
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author | Abuaf, Meir Das, Subhomoy Mastai, Yitzhak |
author_facet | Abuaf, Meir Das, Subhomoy Mastai, Yitzhak |
author_sort | Abuaf, Meir |
collection | PubMed |
description | Chiral polymeric particles (CPPs) were studied extensively in recent years due to their importance in pharmaceutical applications. Here, nanosized CPPs were synthesized and applied as catalysts for direct asymmetric aldol reaction. The CPPs were prepared by miniemulsion or inverse miniemulsion based on various chiral amino acid derivatives and characterized by dynamic light scattering and scanning electron microscopy. The nanoparticles with spherical structure between 250 and 400 nm and high chiral surface area were used as catalysts in the aldol reaction at room temperature without additional solvent. l-tryptophan gave the highest enantiomeric excess, >86% with similar catalytic performance four times. |
format | Online Article Text |
id | pubmed-9817469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-98174692023-01-20 Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction Abuaf, Meir Das, Subhomoy Mastai, Yitzhak RSC Adv Chemistry Chiral polymeric particles (CPPs) were studied extensively in recent years due to their importance in pharmaceutical applications. Here, nanosized CPPs were synthesized and applied as catalysts for direct asymmetric aldol reaction. The CPPs were prepared by miniemulsion or inverse miniemulsion based on various chiral amino acid derivatives and characterized by dynamic light scattering and scanning electron microscopy. The nanoparticles with spherical structure between 250 and 400 nm and high chiral surface area were used as catalysts in the aldol reaction at room temperature without additional solvent. l-tryptophan gave the highest enantiomeric excess, >86% with similar catalytic performance four times. The Royal Society of Chemistry 2023-01-06 /pmc/articles/PMC9817469/ /pubmed/36688059 http://dx.doi.org/10.1039/d2ra07244k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Abuaf, Meir Das, Subhomoy Mastai, Yitzhak Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
title | Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
title_full | Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
title_fullStr | Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
title_full_unstemmed | Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
title_short | Organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
title_sort | organocatalytic chiral polymeric nanoparticles for asymmetric aldol reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817469/ https://www.ncbi.nlm.nih.gov/pubmed/36688059 http://dx.doi.org/10.1039/d2ra07244k |
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