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Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics
A reaction manifold has been discovered in which the chemoselectivity can be altered by switching between neat milling and liquid assisted grinding (LAG) with polar additives. After investigation of the reaction mechanism, it has been established that this switching in reaction pathway is due to the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282732/ https://www.ncbi.nlm.nih.gov/pubmed/30335216 http://dx.doi.org/10.1002/anie.201810141 |
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author | Howard, Joseph L. Brand, Michael C. Browne, Duncan L. |
author_facet | Howard, Joseph L. Brand, Michael C. Browne, Duncan L. |
author_sort | Howard, Joseph L. |
collection | PubMed |
description | A reaction manifold has been discovered in which the chemoselectivity can be altered by switching between neat milling and liquid assisted grinding (LAG) with polar additives. After investigation of the reaction mechanism, it has been established that this switching in reaction pathway is due to the neat mechanochemical conditions exhibiting different kinetics for a key step in the transformation. This proof of concept study demonstrates that mechanochemistry can be used to trap the kinetic product of a reaction. It is envisaged that, if this concept can be successfully applied to other transformations, novel synthetic processes could be discovered and known reaction pathways perturbed or diverted. |
format | Online Article Text |
id | pubmed-6282732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62827322018-12-11 Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics Howard, Joseph L. Brand, Michael C. Browne, Duncan L. Angew Chem Int Ed Engl Communications A reaction manifold has been discovered in which the chemoselectivity can be altered by switching between neat milling and liquid assisted grinding (LAG) with polar additives. After investigation of the reaction mechanism, it has been established that this switching in reaction pathway is due to the neat mechanochemical conditions exhibiting different kinetics for a key step in the transformation. This proof of concept study demonstrates that mechanochemistry can be used to trap the kinetic product of a reaction. It is envisaged that, if this concept can be successfully applied to other transformations, novel synthetic processes could be discovered and known reaction pathways perturbed or diverted. John Wiley and Sons Inc. 2018-11-08 2018-12-03 /pmc/articles/PMC6282732/ /pubmed/30335216 http://dx.doi.org/10.1002/anie.201810141 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Howard, Joseph L. Brand, Michael C. Browne, Duncan L. Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics |
title | Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics |
title_full | Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics |
title_fullStr | Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics |
title_full_unstemmed | Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics |
title_short | Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics |
title_sort | switching chemoselectivity: using mechanochemistry to alter reaction kinetics |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282732/ https://www.ncbi.nlm.nih.gov/pubmed/30335216 http://dx.doi.org/10.1002/anie.201810141 |
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