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Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()

The synthesis of several sulfates of trichothecene mycotoxins is presented. Deoxynivalenol (DON) and its acetylated derivatives were synthesized from 3-acetyldeoxynivalenol (3ADON) and used as substrate for sulfation in order to reach a series of five different DON-based sulfates as well as T2-toxin...

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Autores principales: Fruhmann, Philipp, Skrinjar, Philipp, Weber, Julia, Mikula, Hannes, Warth, Benedikt, Sulyok, Michael, Krska, Rudolf, Adam, Gerhard, Rosenberg, Erwin, Hametner, Christian, Fröhlich, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082130/
https://www.ncbi.nlm.nih.gov/pubmed/25170180
http://dx.doi.org/10.1016/j.tet.2014.05.064
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author Fruhmann, Philipp
Skrinjar, Philipp
Weber, Julia
Mikula, Hannes
Warth, Benedikt
Sulyok, Michael
Krska, Rudolf
Adam, Gerhard
Rosenberg, Erwin
Hametner, Christian
Fröhlich, Johannes
author_facet Fruhmann, Philipp
Skrinjar, Philipp
Weber, Julia
Mikula, Hannes
Warth, Benedikt
Sulyok, Michael
Krska, Rudolf
Adam, Gerhard
Rosenberg, Erwin
Hametner, Christian
Fröhlich, Johannes
author_sort Fruhmann, Philipp
collection PubMed
description The synthesis of several sulfates of trichothecene mycotoxins is presented. Deoxynivalenol (DON) and its acetylated derivatives were synthesized from 3-acetyldeoxynivalenol (3ADON) and used as substrate for sulfation in order to reach a series of five different DON-based sulfates as well as T2-toxin-3-sulfate. These substances are suspected to be formed during phase-II metabolism in plants and humans. The sulfation was performed using a sulfuryl imidazolium salt, which was synthesized prior to use. All protected intermediates and final products were characterized via NMR and will serve as reference materials for further investigations in the fields of toxicology and bioanalytics of mycotoxins.
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spelling pubmed-40821302014-08-26 Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin() Fruhmann, Philipp Skrinjar, Philipp Weber, Julia Mikula, Hannes Warth, Benedikt Sulyok, Michael Krska, Rudolf Adam, Gerhard Rosenberg, Erwin Hametner, Christian Fröhlich, Johannes Tetrahedron Article The synthesis of several sulfates of trichothecene mycotoxins is presented. Deoxynivalenol (DON) and its acetylated derivatives were synthesized from 3-acetyldeoxynivalenol (3ADON) and used as substrate for sulfation in order to reach a series of five different DON-based sulfates as well as T2-toxin-3-sulfate. These substances are suspected to be formed during phase-II metabolism in plants and humans. The sulfation was performed using a sulfuryl imidazolium salt, which was synthesized prior to use. All protected intermediates and final products were characterized via NMR and will serve as reference materials for further investigations in the fields of toxicology and bioanalytics of mycotoxins. Pergamon Press 2014-08-26 /pmc/articles/PMC4082130/ /pubmed/25170180 http://dx.doi.org/10.1016/j.tet.2014.05.064 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Fruhmann, Philipp
Skrinjar, Philipp
Weber, Julia
Mikula, Hannes
Warth, Benedikt
Sulyok, Michael
Krska, Rudolf
Adam, Gerhard
Rosenberg, Erwin
Hametner, Christian
Fröhlich, Johannes
Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()
title Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()
title_full Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()
title_fullStr Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()
title_full_unstemmed Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()
title_short Sulfation of deoxynivalenol, its acetylated derivatives, and T2-toxin()
title_sort sulfation of deoxynivalenol, its acetylated derivatives, and t2-toxin()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082130/
https://www.ncbi.nlm.nih.gov/pubmed/25170180
http://dx.doi.org/10.1016/j.tet.2014.05.064
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