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J Comb Chem ; 9(3): 454-61, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17411098

RESUMEN

An efficient synthesis of unsubstituted and substituted amides based on the 6,8-dioxa-3-azabicyclo[3.2.1]octane scaffold is described. The reaction, carried out at 60 degrees C in the absence of solvent, is characterized by its mildness and ease of workup. A library of amides, was synthesized by combination of methyl esters 1-6 with various amines. In addition, the microwave-assisted automated synthesis of the library was compared with the above conventional parallel synthesis. Microwave synthesis significantly decreased the reaction time from hours to minutes.


Asunto(s)
Amidas/química , Compuestos Bicíclicos Heterocíclicos con Puentes/química , Técnicas Químicas Combinatorias/métodos , Ésteres/síntesis química , Ésteres/química , Estructura Molecular , Estereoisomerismo
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