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Short Total Synthesis of (±)-γ-Lycorane by a Sequential Intramolecular Acylal Cyclisation (IAC) and Intramolecular Heck Addition Reaction.
Monaco, Alessandra; Szulc, Blanka R; Rao, Zenobia X; Barniol-Xicota, Marta; Sehailia, Moussa; Borges, Bruno M A; Hilton, Stephen T.
Afiliação
  • Monaco A; UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
  • Szulc BR; UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
  • Rao ZX; UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
  • Barniol-Xicota M; Laboratori de Química Farmacèutica (Unitat Associada al CSIC), Facultat de Farmàcia, Institute of Biomedicine (IBUB), Universitat de Barcelona, Av. Joan XXIII, s/n, 08028, Barcelona, Spain.
  • Sehailia M; UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
  • Borges BM; UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
  • Hilton ST; UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
Chemistry ; 23(20): 4750-4755, 2017 Apr 06.
Article em En | MEDLINE | ID: mdl-28217842
ABSTRACT
An intramolecular acylal cyclisation (IAC) approach to the synthesis of a range of bicyclic heterocycles is reported. As an example of the utility of the IAC reaction, the methodology was applied in a protecting-group-free five-step total synthesis of (±)-γ-lycorane, incorporating a new intramolecular Heck addition reaction to generate the pentacyclic core structure of the natural product in good yield.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Alcaloides de Amaryllidaceae Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Alcaloides de Amaryllidaceae Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido