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Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins

A number of per-6-substituted cyclodextrin derivative syntheses have been effectively carried out in a planetary ball mill under solvent-free conditions. The preparation of Bridion(®) and important per-6-amino/thiocyclodextrin intermediates without polar aprotic solvents, a source of byproducts and...

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Autores principales: Jicsinszky, Laszlo, Caporaso, Marina, Martina, Katia, Calcio Gaudino, Emanuela, Cravotto, Giancarlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238617/
https://www.ncbi.nlm.nih.gov/pubmed/28144304
http://dx.doi.org/10.3762/bjoc.12.230
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author Jicsinszky, Laszlo
Caporaso, Marina
Martina, Katia
Calcio Gaudino, Emanuela
Cravotto, Giancarlo
author_facet Jicsinszky, Laszlo
Caporaso, Marina
Martina, Katia
Calcio Gaudino, Emanuela
Cravotto, Giancarlo
author_sort Jicsinszky, Laszlo
collection PubMed
description A number of per-6-substituted cyclodextrin derivative syntheses have been effectively carried out in a planetary ball mill under solvent-free conditions. The preparation of Bridion(®) and important per-6-amino/thiocyclodextrin intermediates without polar aprotic solvents, a source of byproducts and persistent impurities, could be performed. Isolation and purification processes could also be simplified. Considerably lower alkylthiol/halide ratio were necessary to reach the complete reaction in comparison with thiourea or azide reactions. While the presented mechanochemical syntheses were carried out on the millimolar scale, they are easily scalable.
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spelling pubmed-52386172017-01-31 Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins Jicsinszky, Laszlo Caporaso, Marina Martina, Katia Calcio Gaudino, Emanuela Cravotto, Giancarlo Beilstein J Org Chem Full Research Paper A number of per-6-substituted cyclodextrin derivative syntheses have been effectively carried out in a planetary ball mill under solvent-free conditions. The preparation of Bridion(®) and important per-6-amino/thiocyclodextrin intermediates without polar aprotic solvents, a source of byproducts and persistent impurities, could be performed. Isolation and purification processes could also be simplified. Considerably lower alkylthiol/halide ratio were necessary to reach the complete reaction in comparison with thiourea or azide reactions. While the presented mechanochemical syntheses were carried out on the millimolar scale, they are easily scalable. Beilstein-Institut 2016-11-10 /pmc/articles/PMC5238617/ /pubmed/28144304 http://dx.doi.org/10.3762/bjoc.12.230 Text en Copyright © 2016, Jicsinszky et al. https://creativecommons.org/licenses/by/4.0https://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/4.0), 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
Jicsinszky, Laszlo
Caporaso, Marina
Martina, Katia
Calcio Gaudino, Emanuela
Cravotto, Giancarlo
Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
title Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
title_full Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
title_fullStr Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
title_full_unstemmed Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
title_short Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
title_sort efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238617/
https://www.ncbi.nlm.nih.gov/pubmed/28144304
http://dx.doi.org/10.3762/bjoc.12.230
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