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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...

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Detalles Bibliográficos
Autores principales: Howard, Joseph L., Brand, Michael C., Browne, Duncan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
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.
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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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