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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...

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Detalles Bibliográficos
Autores principales: Baumann, Marcus, Baxendale, Ian R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
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.
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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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