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Bifunctional phase-transfer catalysis in the asymmetric synthesis of biologically active isoindolinones.
Di Mola, Antonia; Tiffner, Maximilian; Scorzelli, Francesco; Palombi, Laura; Filosa, Rosanna; De Caprariis, Paolo; Waser, Mario; Massa, Antonio.
Afiliação
  • Di Mola A; Dipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy; Dipartimento di Farmacia, Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy.
  • Tiffner M; Institute of Organic Chemistry, Johannes Kepler University Linz Altenbergerstraße 69, 4040 Linz, Austria.
  • Scorzelli F; Dipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy.
  • Palombi L; Dipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy.
  • Filosa R; Dipartimento di Medicina Sperimentale, Università di Napoli, Napoli, Italy.
  • De Caprariis P; Dipartimento di Farmacia, Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy.
  • Waser M; Institute of Organic Chemistry, Johannes Kepler University Linz Altenbergerstraße 69, 4040 Linz, Austria.
  • Massa A; Dipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy.
Beilstein J Org Chem ; 11: 2591-9, 2015.
Article em En | MEDLINE | ID: mdl-26734105
ABSTRACT
New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key building block for a variety of biologically relevant isoindolinones. With this chiral compound in hand, the development of further transformations allowed for the synthesis of diverse derivatives of high pharmaceutical value, such as the Belliotti (S)-PD172938 and arylated analogues with hypnotic sedative activity, obtained in good overall total yield (50%) and high enantiomeric purity (95% ee). The synthetic routes developed herein are particularly convenient in comparison with the current methods available in literature and are particularly promising for large scale applications.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article