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Bioorg Med Chem ; 24(21): 5249-5257, 2016 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-27622748

RESUMEN

In order to address the current downturn in the drug discovery pipeline, initiatives are being undertaken to synthesise screening libraries of sp3-rich, low molecular weight compounds. As part of the European Lead Factory initiative, the synthesis and derivatisation of a simple hexahydrooxazolo[5,4-c]pyridin-2(1H)-one bicyclic carbamate has been achieved. The synthetic route employed involved a telescoped hetero-Diels-Alder/[2,3]-sigmatropic rearrangement/cyclisation sequence to deliver the desired core scaffold containing two points for further diversification. When applied, this synthesis was found to be robust and scalable which allowed the production of a 155 compound library.


Asunto(s)
Oxazolidinonas/síntesis química , Bibliotecas de Moléculas Pequeñas/síntesis química , Cristalografía por Rayos X , Modelos Moleculares , Estructura Molecular , Oxazolidinonas/química , Bibliotecas de Moléculas Pequeñas/química
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