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A simplified and scalable synthesis of artesunate
ABSTRACT: An efficient and economically viable approach for the large-scale conversion of artemisinin into the antimalarial frontline drug artesunate was developed. This advanced synthesis includes an NaBH(4)-induced reduction, followed by an esterification with succinic anhydride under basic condit...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225229/ https://www.ncbi.nlm.nih.gov/pubmed/28127092 http://dx.doi.org/10.1007/s00706-016-1865-9 |
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author | Presser, Armin Feichtinger, Andrea Buzzi, Silke |
author_facet | Presser, Armin Feichtinger, Andrea Buzzi, Silke |
author_sort | Presser, Armin |
collection | PubMed |
description | ABSTRACT: An efficient and economically viable approach for the large-scale conversion of artemisinin into the antimalarial frontline drug artesunate was developed. This advanced synthesis includes an NaBH(4)-induced reduction, followed by an esterification with succinic anhydride under basic conditions. The entire conversion follows the principles of green chemistry, i.e., application of reusable solvents. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-5225229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-52252292017-01-24 A simplified and scalable synthesis of artesunate Presser, Armin Feichtinger, Andrea Buzzi, Silke Monatsh Chem Original Paper ABSTRACT: An efficient and economically viable approach for the large-scale conversion of artemisinin into the antimalarial frontline drug artesunate was developed. This advanced synthesis includes an NaBH(4)-induced reduction, followed by an esterification with succinic anhydride under basic conditions. The entire conversion follows the principles of green chemistry, i.e., application of reusable solvents. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2016-12-02 2017 /pmc/articles/PMC5225229/ /pubmed/28127092 http://dx.doi.org/10.1007/s00706-016-1865-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Presser, Armin Feichtinger, Andrea Buzzi, Silke A simplified and scalable synthesis of artesunate |
title | A simplified and scalable synthesis of artesunate |
title_full | A simplified and scalable synthesis of artesunate |
title_fullStr | A simplified and scalable synthesis of artesunate |
title_full_unstemmed | A simplified and scalable synthesis of artesunate |
title_short | A simplified and scalable synthesis of artesunate |
title_sort | simplified and scalable synthesis of artesunate |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225229/ https://www.ncbi.nlm.nih.gov/pubmed/28127092 http://dx.doi.org/10.1007/s00706-016-1865-9 |
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