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Switching Chemoselectivity: Using Mechanochemistry to Alter Reaction Kinetics.
Howard, Joseph L; Brand, Michael C; Browne, Duncan L.
Afiliação
  • Howard JL; School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3EQ, UK.
  • Brand MC; School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3EQ, UK.
  • Browne DL; School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3EQ, UK.
Angew Chem Int Ed Engl ; 57(49): 16104-16108, 2018 Dec 03.
Article em En | MEDLINE | ID: mdl-30335216
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido