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Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction

A versatile continuous-flow synthesis of highly functionalized 1,2,4-oxadiazoles starting from carboxylic acids is reported. This process was applied to the multistep synthesis of imidazo[1,2-a]pyridin-2-yl-1,2,4-oxadiazoles, using a three reactor, multistep continuous-flow system without isolation...

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Detalles Bibliográficos
Autores principales: Herath, Ananda, Cosford, Nicholas D P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331298/
https://www.ncbi.nlm.nih.gov/pubmed/28326132
http://dx.doi.org/10.3762/bjoc.13.26
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author Herath, Ananda
Cosford, Nicholas D P
author_facet Herath, Ananda
Cosford, Nicholas D P
author_sort Herath, Ananda
collection PubMed
description A versatile continuous-flow synthesis of highly functionalized 1,2,4-oxadiazoles starting from carboxylic acids is reported. This process was applied to the multistep synthesis of imidazo[1,2-a]pyridin-2-yl-1,2,4-oxadiazoles, using a three reactor, multistep continuous-flow system without isolation of intermediates. This continuous-flow method was successfully combined with a single-step liquid–liquid microextraction unit to remove high boiling point polar solvents and impurities and provides the target compounds in high purity with excellent overall yields.
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spelling pubmed-53312982017-03-21 Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction Herath, Ananda Cosford, Nicholas D P Beilstein J Org Chem Full Research Paper A versatile continuous-flow synthesis of highly functionalized 1,2,4-oxadiazoles starting from carboxylic acids is reported. This process was applied to the multistep synthesis of imidazo[1,2-a]pyridin-2-yl-1,2,4-oxadiazoles, using a three reactor, multistep continuous-flow system without isolation of intermediates. This continuous-flow method was successfully combined with a single-step liquid–liquid microextraction unit to remove high boiling point polar solvents and impurities and provides the target compounds in high purity with excellent overall yields. Beilstein-Institut 2017-02-07 /pmc/articles/PMC5331298/ /pubmed/28326132 http://dx.doi.org/10.3762/bjoc.13.26 Text en Copyright © 2017, Herath and Cosford 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
Herath, Ananda
Cosford, Nicholas D P
Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
title Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
title_full Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
title_fullStr Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
title_full_unstemmed Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
title_short Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
title_sort continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331298/
https://www.ncbi.nlm.nih.gov/pubmed/28326132
http://dx.doi.org/10.3762/bjoc.13.26
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