A general synthetic approach to the amnesic shellfish toxins: total synthesis of (−)-isodomoic acid B, (−)-isodomoic acid E and (−)-isodomoic acid F

Autor: Simon Sedehizadeh, Nadia Fleary-Roberts, Gilles Lemière, Jonathan Clayden, Julie Toueg
Rok vydání: 2011
Předmět:
Zdroj: Lemière, G, Sedehizadeh, S, Toueg, J, Fleary-Roberts, N & Clayden, J 2011, ' A general synthetic approach to the amnesic shellfish toxins: Total synthesis of (-)-isodomoic acid B, (-)-isodomoic acid E and (-)-isodomoic acid F ', Chemical Communications, vol. 47, no. 13, pp. 3745-3747 . https://doi.org/10.1039/c1cc00048a
ISSN: 1364-548X
1359-7345
Popis: The alkynylpyrrolidine 4 was made via a dearomatising cyclisation of an aromatic amide, and was elaborated by stannylcupration and palladium-catalysed coupling to achieve the first total synthesis of three members of the isodomoic acid family; the same alkyne can be envisaged as a precursor to several more of this class of amnesic shellfish toxins. © The Royal Society of Chemistry.
Databáze: OpenAIRE