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A new synthetic protocol for coumarin amino acid
The hydrochloride of the racemic amino acid (2-(7-hydroxycoumarin-4-yl)ethyl)glycine, which can serve as a fluorescent probe in proteins, and two halogen derivatives of it, were synthesized by using a new synthetic protocol in five steps. It is less costly and relatively easy to prepare this kind of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566773/ https://www.ncbi.nlm.nih.gov/pubmed/23400513 http://dx.doi.org/10.3762/bjoc.9.30 |
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author | Xu, Xinyi Hu, Xiaosong Wang, Jiangyun |
author_facet | Xu, Xinyi Hu, Xiaosong Wang, Jiangyun |
author_sort | Xu, Xinyi |
collection | PubMed |
description | The hydrochloride of the racemic amino acid (2-(7-hydroxycoumarin-4-yl)ethyl)glycine, which can serve as a fluorescent probe in proteins, and two halogen derivatives of it, were synthesized by using a new synthetic protocol in five steps. It is less costly and relatively easy to prepare this kind of fluorescent amino acid with the new synthetic method. Furthermore, it can be applied to synthesize other derivatives of the coumarin amino acid with some specific properties. |
format | Online Article Text |
id | pubmed-3566773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-35667732013-02-11 A new synthetic protocol for coumarin amino acid Xu, Xinyi Hu, Xiaosong Wang, Jiangyun Beilstein J Org Chem Full Research Paper The hydrochloride of the racemic amino acid (2-(7-hydroxycoumarin-4-yl)ethyl)glycine, which can serve as a fluorescent probe in proteins, and two halogen derivatives of it, were synthesized by using a new synthetic protocol in five steps. It is less costly and relatively easy to prepare this kind of fluorescent amino acid with the new synthetic method. Furthermore, it can be applied to synthesize other derivatives of the coumarin amino acid with some specific properties. Beilstein-Institut 2013-02-06 /pmc/articles/PMC3566773/ /pubmed/23400513 http://dx.doi.org/10.3762/bjoc.9.30 Text en Copyright © 2013, Xu et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Xu, Xinyi Hu, Xiaosong Wang, Jiangyun A new synthetic protocol for coumarin amino acid |
title | A new synthetic protocol for coumarin amino acid |
title_full | A new synthetic protocol for coumarin amino acid |
title_fullStr | A new synthetic protocol for coumarin amino acid |
title_full_unstemmed | A new synthetic protocol for coumarin amino acid |
title_short | A new synthetic protocol for coumarin amino acid |
title_sort | new synthetic protocol for coumarin amino acid |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566773/ https://www.ncbi.nlm.nih.gov/pubmed/23400513 http://dx.doi.org/10.3762/bjoc.9.30 |
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