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The rapid generation of isothiocyanates in flow
Isothiocyanates are versatile starting materials for a wide range of chemical reactions. However, their high nucleophilic susceptibility means they are best prepared and used immediately. We report here on a flow platform for the fast and efficient formation of isothiocyanates by the direct conversi...
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/PMC3778409/ https://www.ncbi.nlm.nih.gov/pubmed/24062820 http://dx.doi.org/10.3762/bjoc.9.184 |
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author | Baumann, Marcus Baxendale, Ian R |
author_facet | Baumann, Marcus Baxendale, Ian R |
author_sort | Baumann, Marcus |
collection | PubMed |
description | Isothiocyanates are versatile starting materials for a wide range of chemical reactions. However, their high nucleophilic susceptibility means they are best prepared and used immediately. We report here on a flow platform for the fast and efficient formation of isothiocyanates by the direct conversion of easily prepared chloroximes. To expedite this chemistry a flow insert cartridge containing two immobilised reagents is used to affect the chemical transformation which typically eliminates the requirements for any conventional work-up or purification of the reaction stream. |
format | Online Article Text |
id | pubmed-3778409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-37784092013-09-23 The rapid generation of isothiocyanates in flow Baumann, Marcus Baxendale, Ian R Beilstein J Org Chem Full Research Paper Isothiocyanates are versatile starting materials for a wide range of chemical reactions. However, their high nucleophilic susceptibility means they are best prepared and used immediately. We report here on a flow platform for the fast and efficient formation of isothiocyanates by the direct conversion of easily prepared chloroximes. To expedite this chemistry a flow insert cartridge containing two immobilised reagents is used to affect the chemical transformation which typically eliminates the requirements for any conventional work-up or purification of the reaction stream. Beilstein-Institut 2013-08-08 /pmc/articles/PMC3778409/ /pubmed/24062820 http://dx.doi.org/10.3762/bjoc.9.184 Text en Copyright © 2013, Baumann and Baxendale 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 Baumann, Marcus Baxendale, Ian R The rapid generation of isothiocyanates in flow |
title | The rapid generation of isothiocyanates in flow |
title_full | The rapid generation of isothiocyanates in flow |
title_fullStr | The rapid generation of isothiocyanates in flow |
title_full_unstemmed | The rapid generation of isothiocyanates in flow |
title_short | The rapid generation of isothiocyanates in flow |
title_sort | rapid generation of isothiocyanates in flow |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778409/ https://www.ncbi.nlm.nih.gov/pubmed/24062820 http://dx.doi.org/10.3762/bjoc.9.184 |
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