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Enantioconvergent alkylation of ketones with racemic secondary alcohols via hydrogen borrowing catalysis.
Cheang, Daniella M J; Armstrong, Roly J; Akhtar, Wasim M; Donohoe, Timothy J.
Afiliación
  • Cheang DMJ; Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK. timothy.donohoe@chem.ox.ac.uk.
  • Armstrong RJ; Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK. timothy.donohoe@chem.ox.ac.uk.
  • Akhtar WM; Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK. timothy.donohoe@chem.ox.ac.uk.
  • Donohoe TJ; Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK. timothy.donohoe@chem.ox.ac.uk.
Chem Commun (Camb) ; 56(24): 3543-3546, 2020 Mar 24.
Article en En | MEDLINE | ID: mdl-32104853
An enantioconvergent method for the alkylation of o-disubstituted aryl ketones with racemic secondary alcohols is described. This process is mediated by a commercially available iridium catalyst and proceeds via hydrogen borrowing catalysis. The highly enantioenriched ß-substituted ketone products were readily cleaved to a wide range of functional groups via retro-Friedel-Crafts acylation.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2020 Tipo del documento: Article
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